-
1
-
-
0345746381
-
A magic bullet: Research for profit and the growth of knowledge in Germany around 1900
-
[CrossRef]
-
Lenoir, T. A magic bullet: Research for profit and the growth of knowledge in Germany around 1900. Minerva 1988, 26, 66–88. [CrossRef].
-
(1988)
Minerva
, vol.26
, pp. 66-88
-
-
Lenoir, T.1
-
2
-
-
74949107560
-
Antibody-drug conjugates: Linking cytotoxic payloads to monoclonal antibodies
-
Laurent, D.; Bernhard, S. Antibody-drug conjugates: Linking cytotoxic payloads to monoclonal antibodies. Bioconjug. Chem. 2010, 21, 5–13.
-
(2010)
Bioconjug. Chem
, vol.21
, pp. 5-13
-
-
Laurent, D.1
Bernhard, S.2
-
3
-
-
84903762549
-
Antibody-drug conjugates: Current status and future directions
-
[CrossRef] [PubMed]
-
Perez, H.L.; Cardarelli, P.M.; Deshpande, S.; Gangwar, S.; Schroeder, G.M.; Vite, G.D.; Borzilleri, R.M. Antibody-drug conjugates: Current status and future directions. Drug Discov. Today 2014, 19, 869–881. [CrossRef] [PubMed].
-
(2014)
Drug Discov. Today
, vol.19
, pp. 869-881
-
-
Perez, H.L.1
Cardarelli, P.M.2
Deshpande, S.3
Gangwar, S.4
Schroeder, G.M.5
Vite, G.D.6
Borzilleri, R.M.7
-
4
-
-
84898066972
-
Antibody-drug conjugates: An emerging concept in cancer therapy
-
[CrossRef] [PubMed]
-
Chari, R.V.J.; Miller, M. L.; Widdison, W.C. Antibody-drug conjugates: An emerging concept in cancer therapy. Angew. Chem. Int. Ed. Engl. 2014, 53, 3796–3827. [CrossRef] [PubMed].
-
(2014)
Angew. Chem. Int. Ed. Engl
, vol.53
, pp. 3796-3827
-
-
Chari, R.V.J.1
Miller, M.L.2
Widdison, W.C.3
-
5
-
-
84872861443
-
American association of pharmaceutical scientists national biotechnology conference short course: Translational challenges in developing antibody-drug conjugates
-
[CrossRef]
-
Thudium, K.; Bilic, S.; Leipold, D.; Mallet, W.; Kaur, S.; Meibohm, B.; Erickson, H.; Tibbitts, J.; Zhao, H.; Gupta, M. American association of pharmaceutical scientists national biotechnology conference short course: Translational challenges in developing antibody-drug conjugates. MAbs 2013, 5, 5–12. [CrossRef].
-
(2013)
Mabs
, vol.5
, pp. 5-12
-
-
Thudium, K.1
Bilic, S.2
Leipold, D.3
Mallet, W.4
Kaur, S.5
Meibohm, B.6
Erickson, H.7
Tibbitts, J.8
Zhao, H.9
Gupta, M.10
-
6
-
-
84873053339
-
Antibody-drug conjugates in cancer therapy
-
[CrossRef] [PubMed]
-
Sievers, E.L.; Senter, P.D. Antibody-drug conjugates in cancer therapy. Annu. Rev. Med. 2013, 64, 15–29. [CrossRef] [PubMed].
-
(2013)
Annu. Rev. Med
, vol.64
, pp. 15-29
-
-
Sievers, E.L.1
Senter, P.D.2
-
7
-
-
84934444193
-
Selecting an optimal antibody for antibody-drug conjugate therapy: Internalization and intracellular localization
-
[PubMed]
-
Harper, J.; Mao, S.; Strout, P.; Kamal, A. Selecting an optimal antibody for antibody-drug conjugate therapy: Internalization and intracellular localization. Methods Mol. Biol. 2013, 1045, 41–49. [PubMed].
-
(2013)
Methods Mol. Biol
, vol.1045
, pp. 41-49
-
-
Harper, J.1
Mao, S.2
Strout, P.3
Kamal, A.4
-
8
-
-
84934442221
-
Antibody-drug conjugate target selection: Critical factors
-
[PubMed]
-
Bander, N.H. Antibody-drug conjugate target selection: Critical factors. Methods Mol. Biol. 2013, 1045, 29–40. [PubMed].
-
(2013)
Methods Mol. Biol
, vol.1045
, pp. 29-40
-
-
Bander, N.H.1
-
9
-
-
84879591299
-
The antibody-drug conjugate: An enabling modality for natural product-based cancer therapeutics
-
[CrossRef] [PubMed]
-
Gerber, H.-P.; Koehn, F.E.; Abraham, R.T. The antibody-drug conjugate: An enabling modality for natural product-based cancer therapeutics. Nat. Prod. Rep. 2013, 30, 625–639. [CrossRef] [PubMed].
-
(2013)
Nat. Prod. Rep
, vol.30
, pp. 625-639
-
-
Gerber, H.-P.1
Koehn, F.E.2
Abraham, R.T.3
-
10
-
-
84955494300
-
Recent advances in the construction of antibody–drug conjugates
-
[CrossRef]
-
Chudasama, V.; Maruani, A.; Caddick, S. Recent advances in the construction of antibody–drug conjugates. Nat. Chem. 2016, 8, 114–119. [CrossRef].
-
(2016)
Nat. Chem
, vol.8
, pp. 114-119
-
-
Chudasama, V.1
Maruani, A.2
Caddick, S.3
-
11
-
-
84953431794
-
Antibody-drug conjugates—An emerging class of cancer treatment
-
[CrossRef] [PubMed]
-
Diamantis, N.; Banerji, U. Antibody-drug conjugates—An emerging class of cancer treatment. Br. J. Cancer 2016. [CrossRef] [PubMed].
-
(2016)
Br. J. Cancer
-
-
Diamantis, N.1
Banerji, U.2
-
12
-
-
37548998932
-
Contributions of a disulfide bond to the structure, stability, and dimerization of human IgG1 antibody CH3 domain
-
[CrossRef] [PubMed]
-
McAuley, A.; Jacob, J.; Kolvenbach, C.G.; Westland, K.; Lee, H.J.; Brych, S.R.; Rehder, D.; Kleemann, G.R.; Brems, D.N.; Matsumura, M. Contributions of a disulfide bond to the structure, stability, and dimerization of human IgG1 antibody CH3 domain. Protein Sci. 2008, 17, 95–106. [CrossRef] [PubMed].
-
(2008)
Protein Sci.
, vol.17
, pp. 95-106
-
-
McAuley, A.1
Jacob, J.2
Kolvenbach, C.G.3
Westland, K.4
Lee, H.J.5
Brych, S.R.6
Rehder, D.7
Kleemann, G.R.8
Brems, D.N.9
Matsumura, M.10
-
13
-
-
25444507922
-
Reduction–alkylation strategies for the modification of specific monoclonal antibody disulfides
-
[CrossRef] [PubMed]
-
Sun, M.M.C.; Beam, K.S.; Cerveny, C.G.; Hamblett, K.J.; Blackmore, R.S.; Torgov, M.Y.; Handley, F.G.M.; Ihle, N.C.; Senter, P.D.; Alley, S.C. Reduction–alkylation strategies for the modification of specific monoclonal antibody disulfides. Bioconjug. Chem. 2005, 16, 1282–1290. [CrossRef] [PubMed].
-
(2005)
Bioconjug. Chem
, vol.16
, pp. 1282-1290
-
-
Sun, M.M.C.1
Beam, K.S.2
Cerveny, C.G.3
Hamblett, K.J.4
Blackmore, R.S.5
Torgov, M.Y.6
Handley, F.G.M.7
Ihle, N.C.8
Senter, P.D.9
Alley, S.C.10
-
14
-
-
0027134326
-
(6-Maleimidocaproyl) hydrazone of doxorubicin-a new derivative for the preparation of immunoconjugates of doxorubicin
-
[CrossRef] [PubMed]
-
Willner, D.; Trail, P.A.; Hofstead, S.J.; King, H.D.; Lasch, S.J.; Braslawsky, G.R.; Greenfield, R.S.; Kaneko, T.; Firestone, R.A. (6-Maleimidocaproyl) hydrazone of doxorubicin-a new derivative for the preparation of immunoconjugates of doxorubicin. Bioconjug. Chem. 1993, 4, 521–527. [CrossRef] [PubMed].
-
(1993)
Bioconjug. Chem
, vol.4
, pp. 521-527
-
-
Willner, D.1
Trail, P.A.2
Hofstead, S.J.3
King, H.D.4
Lasch, S.J.5
Braslawsky, G.R.6
Greenfield, R.S.7
Kaneko, T.8
Firestone, R.A.9
-
15
-
-
10744222473
-
Development of potent monoclonal antibody auristatin conjugates for cancer therapy
-
[CrossRef]
-
Doronina, S.O.; Toki, B.E.; Torgov, M.Y.; Mendelsohn, B.A.; Cerveny, C.G.; Chace, D.F.; DeBlanc, R.L.; Gearing, R.P.; Bovee, T.D.; Siegall, C.B.; et al. Development of potent monoclonal antibody auristatin conjugates for cancer therapy. Nat. Biotechnol. 2003, 21, 778–784. [CrossRef].
-
(2003)
Nat. Biotechnol
, vol.21
, pp. 778-784
-
-
Doronina, S.O.1
Toki, B.E.2
Torgov, M.Y.3
Mendelsohn, B.A.4
Cerveny, C.G.5
Chace, D.F.6
Deblanc, R.L.7
Gearing, R.P.8
Bovee, T.D.9
Siegall, C.B.10
-
16
-
-
0042738861
-
CAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity
-
[CrossRef] [PubMed]
-
Francisco, J.A.; Cerveny, C.G.; Meyer, D.L.; Mixan, B.J.; Klussman, K.; Chace, D.F.; Rejniak, S.X.; Gordon, K.A.; DeBlanc, R.; Toki, B.E.; et al. cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. Blood 2003, 102, 1458–1465. [CrossRef] [PubMed].
-
(2003)
Blood
, vol.102
, pp. 1458-1465
-
-
Francisco, J.A.1
Cerveny, C.G.2
Meyer, D.L.3
Mixan, B.J.4
Klussman, K.5
Chace, D.F.6
Rejniak, S.X.7
Gordon, K.A.8
Deblanc, R.9
Toki, B.E.10
-
17
-
-
6044223544
-
Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate
-
[CrossRef] [PubMed]
-
Hamblett, K.J.; Senter, P.D.; Chace, D.F.; Sun, M.M.C.; Lenox, J.; Cerveny, C.G.; Kissler, K.M.; Bernhardt, S.X.; Kopcha, A.K.; Zabinski, R.F.; et al. Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate. Clin. Cancer Res. 2004, 10, 7063–7070. [CrossRef] [PubMed].
-
(2004)
Clin. Cancer Res
, vol.10
, pp. 7063-7070
-
-
Hamblett, K.J.1
Senter, P.D.2
Chace, D.F.3
Sun, M.M.C.4
Lenox, J.5
Cerveny, C.G.6
Kissler, K.M.7
Bernhardt, S.X.8
Kopcha, A.K.9
Zabinski, R.F.10
-
18
-
-
33745684533
-
Engineered antibody-drug conjugates with defined sites and stoichiometries of drug attachment
-
[CrossRef] [PubMed]
-
McDonagh, C.F.; Turcott, E.; Westendorf, L.; Webster, J.B.; Alley, S.C.; Kim, K.; Andreyka, J.; Stone, I.; Hamblett, K.J.; Francisco, J.A.; et al. Engineered antibody-drug conjugates with defined sites and stoichiometries of drug attachment. Prot. Eng. Des. Sel. 2006, 19, 299–307. [CrossRef] [PubMed].
-
(2006)
Prot. Eng. Des. Sel.
, vol.19
, pp. 299-307
-
-
McDonagh, C.F.1
Turcott, E.2
Westendorf, L.3
Webster, J.B.4
Alley, S.C.5
Kim, K.6
Andreyka, J.7
Stone, I.8
Hamblett, K.J.9
Francisco, J.A.10
-
19
-
-
4644309963
-
Production technologies for monoclonal antibodies and their fragments
-
[CrossRef] [PubMed]
-
Andersen, D.C.; Reilly, D.E. Production technologies for monoclonal antibodies and their fragments. Curr. Opin. Biotechnol. 2004, 15, 456–462. [CrossRef] [PubMed].
-
(2004)
Curr. Opin. Biotechnol.
, vol.15
, pp. 456-462
-
-
Andersen, D.C.1
Reilly, D.E.2
-
20
-
-
0019406560
-
A new preparation of modified immune serum globulin (Human) suitable for intravenous administration. I. Standardization of the reduction and alkylation reaction
-
[CrossRef] [PubMed]
-
Schroeder, D.D.; Tankersly, D.L.; Lundblad, J.L. A new preparation of modified immune serum globulin (human) suitable for intravenous administration. I. Standardization of the reduction and alkylation reaction. Vox. Sang. 1981, 40, 373–382. [CrossRef] [PubMed].
-
(1981)
Vox. Sang.
, vol.40
, pp. 373-382
-
-
Schroeder, D.D.1
Tankersly, D.L.2
Lundblad, J.L.3
-
21
-
-
77953603827
-
Ranking the susceptibility of disulfide bonds in human IgG1 antibodies by reduction, differential alkylation, and LC-MS analysis
-
[CrossRef]
-
Liu, H.; Chumsae, C.; Gaza-Bulseco, G.; Hurkmans, K.; Radziejewski, C.H. Ranking the susceptibility of disulfide bonds in human IgG1 antibodies by reduction, differential alkylation, and LC-MS analysis. Anal. Chem. 2010, 82, 5219–5226. [CrossRef].
-
(2010)
Anal. Chem
, vol.82
, pp. 5219-5226
-
-
Liu, H.1
Chumsae, C.2
Gaza-Bulseco, G.3
Hurkmans, K.4
Radziejewski, C.H.5
-
22
-
-
84863230506
-
Preparation of cystamine core dendrimer and antibody_dendrimer conjugates for MRI angiography
-
[CrossRef] [PubMed]
-
Nwe, K.; Milenic, D.E.; Ray, G.L.; Kim, Y.-S.; Brechbiel, M.W. Preparation of cystamine core dendrimer and antibody_dendrimer conjugates for MRI angiography. Mol. Pharm. 2012, 9, 374–381. [CrossRef] [PubMed].
-
(2012)
Mol. Pharm
, vol.9
, pp. 374-381
-
-
Nwe, K.1
Milenic, D.E.2
Ray, G.L.3
Kim, Y.-S.4
Brechbiel, M.W.5
-
23
-
-
84866353023
-
Therapeutic anti-methamphetamine antibody fragment-nanoparticle conjugates: Synthesis and in vitro characterization
-
[CrossRef] [PubMed]
-
Nanaware-Kharade, N.; Gonzalez, G.A.; Lay, J.O.; Hendrickson, H.P.; Peterson, E.C. Therapeutic anti-methamphetamine antibody fragment-nanoparticle conjugates: Synthesis and in vitro characterization. Bioconjug. Chem. 2012, 23, 1864–1872. [CrossRef] [PubMed].
-
(2012)
Bioconjug. Chem.
, vol.23
, pp. 1864-1872
-
-
Nanaware-Kharade, N.1
Gonzalez, G.A.2
Lay, J.O.3
Hendrickson, H.P.4
Peterson, E.C.5
-
24
-
-
85013795111
-
-
2nd ed.; Academic Press: New York, NY, USA
-
Hermanson, G.T. Bioconjugate Techniques, 2nd ed.; Academic Press: New York, NY, USA, 2008; pp. 1041–1132.
-
(2008)
Bioconjugate Techniques
, pp. 1041-1132
-
-
Hermanson, G.T.1
-
25
-
-
44849088699
-
Peptide/protein-polymer conjugates: Synthetic strategies and design concepts
-
[CrossRef] [PubMed]
-
Gauthier, M.A.; Klok, H.-A. Peptide/protein-polymer conjugates: Synthetic strategies and design concepts. Chem. Commun. 2008, 21, 2591–2611. [CrossRef] [PubMed].
-
(2008)
Chem. Commun
, vol.21
, pp. 2591-2611
-
-
Gauthier, M.A.1
Klok, H.-A.2
-
26
-
-
84863012529
-
Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates
-
[CrossRef] [PubMed]
-
Shen, B.-Q.; Xu, K.; Liu, L.; Raab, H.; Bhakta, S.; Kenrick, M.; Parsons-Reponte, K.L.; Tien, J.; Yu, S.-F.; Mai, E.; et al. Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates. Nat. Biotechnol. 2012, 30, 184–189. [CrossRef] [PubMed].
-
(2012)
Nat. Biotechnol
, vol.30
, pp. 184-189
-
-
Shen, B.-Q.1
Xu, K.2
Liu, L.3
Raab, H.4
Bhakta, S.5
Kenrick, M.6
Parsons-Reponte, K.L.7
Tien, J.8
Yu, S.-F.9
Mai, E.10
-
27
-
-
84934976018
-
Functional native disulfide bridging enables delivery of a potent, stable and targeted antibody_drug conjugate (ADC)
-
[CrossRef] [PubMed]
-
Nunes, J.P.M.; Morais, M.; Vassileva, V.; Robinson, E.; Rajkumar, V.S.; Smith, M.E.B.; Pedley, R.B.; Caddick, S.; Baker, J.R.; Chudasama, V. Functional native disulfide bridging enables delivery of a potent, stable and targeted antibody_drug conjugate (ADC). Chem. Commun. 2015, 51, 10624–10627. [CrossRef] [PubMed].
-
(2015)
Chem. Commun
, vol.51
, pp. 10624-10627
-
-
Nunes, J.P.M.1
Morais, M.2
Vassileva, V.3
Robinson, E.4
Rajkumar, V.S.5
Smith, M.E.B.6
Pedley, R.B.7
Caddick, S.8
Baker, J.R.9
Chudasama, V.10
-
28
-
-
84921407368
-
Self-hydrolyzing maleimides improve the stability and pharmacological properties of antibody-drug conjugates
-
[CrossRef] [PubMed]
-
Lyon, R.P.; Setter, J.R.; Bovee, T.D.; Doronina, S.O.; Hunter, J.H.; Anderson, M.E.; Balasubramanian, C.L.; Duniho, S.M.; Leiske, C.I.; Li, F.; et al. Self-hydrolyzing maleimides improve the stability and pharmacological properties of antibody-drug conjugates. Nat. Biotechnol. 2014, 32, 1059–1062. [CrossRef] [PubMed].
-
(2014)
Nat. Biotechnol
, vol.32
, pp. 1059-1062
-
-
Lyon, R.P.1
Setter, J.R.2
Bovee, T.D.3
Doronina, S.O.4
Hunter, J.H.5
Anderson, M.E.6
Balasubramanian, C.L.7
Duniho, S.M.8
Leiske, C.I.9
Li, F.10
-
29
-
-
84908052265
-
Mild method for succinimide hydrolysis on ADCs: Impact on ADC potency, stability, exposure, and efficacy
-
[CrossRef] [PubMed]
-
Tumey, L.N.; Charati, M.; He, T.; Sousa, E.; Ma, D.; Han, X.; Clark, T.; Casavant, J.; Loganzo, F.; Barletta, F.; et al. Mild method for succinimide hydrolysis on ADCs: Impact on ADC potency, stability, exposure, and efficacy. Bioconjug. Chem. 2014, 25, 1871–1880. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 1871-1880
-
-
Tumey, L.N.1
Charati, M.2
He, T.3
Sousa, E.4
Ma, D.5
Han, X.6
Clark, T.7
Casavant, J.8
Loganzo, F.9
Barletta, F.10
-
30
-
-
0037137606
-
Tumor-specific novel taxoid-monoclonal antibody conjugates
-
[CrossRef] [PubMed]
-
Ojima, I.; Geng, X.; Wu, X.; Qu, C.; Borella, C.P.; Xie, H.; Wilhelm, S.D.; Leece, B.A.; Bartle, L.M.; Goldmacher, V.S.; et al. Tumor-specific novel taxoid-monoclonal antibody conjugates. J. Med. Chem. 2002, 45, 5620–5623. [CrossRef] [PubMed].
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5620-5623
-
-
Ojima, I.1
Geng, X.2
Wu, X.3
Qu, C.4
Borella, C.P.5
Xie, H.6
Wilhelm, S.D.7
Leece, B.A.8
Bartle, L.M.9
Goldmacher, V.S.10
-
31
-
-
33745847797
-
Semisynthetic maytansine analogues for the targeted treatment of cancer
-
[CrossRef] [PubMed]
-
Widdison, W.C.; Wilhelm, S.D.; Cavanagh, E.E.; Whiteman, K.R.; Leece, B.A.; Kovtun, Y.; Goldmacher, V.S.; Xie, H.; Steeves, R.M.; Lutz, R.J.; et al. Semisynthetic maytansine analogues for the targeted treatment of cancer. J. Med. Chem. 2006, 49, 4392–4408. [CrossRef] [PubMed].
-
(2006)
J. Med. Chem
, vol.49
, pp. 4392-4408
-
-
Widdison, W.C.1
Wilhelm, S.D.2
Cavanagh, E.E.3
Whiteman, K.R.4
Leece, B.A.5
Kovtun, Y.6
Goldmacher, V.S.7
Xie, H.8
Steeves, R.M.9
Lutz, R.J.10
-
32
-
-
84923225838
-
CBTF: New amine-to-thiol coupling reagent for preparation of antibody conjugates with increased plasma stability
-
[CrossRef] [PubMed]
-
Kolodych, S.; Koniev, O.; Baatarkhuu, Z.; Bonnefoy, J.-Y.; Debaene, F.; Cianférani, S.; Dorsselaer, A.V.; Wagner, A. CBTF: New amine-to-thiol coupling reagent for preparation of antibody conjugates with increased plasma stability. Bioconjug. Chem. 2015, 26, 197–200. [CrossRef] [PubMed].
-
(2015)
Bioconjug. Chem
, vol.26
, pp. 197-200
-
-
Kolodych, S.1
Koniev, O.2
Baatarkhuu, Z.3
Bonnefoy, J.-Y.4
Debaene, F.5
Cianférani, S.6
Dorsselaer, A.V.7
Wagner, A.8
-
33
-
-
84922713475
-
Cysteine-selective reactions for antibody conjugation
-
[CrossRef] [PubMed]
-
Cal, P.M.; Bernardes, G.J.; Gois, P.M. Cysteine-selective reactions for antibody conjugation. Angew. Chem. Int. Ed. Engl. 2014, 53, 10585–10587. [CrossRef] [PubMed].
-
(2014)
Angew. Chem. Int. Ed. Engl
, vol.53
, pp. 10585-10587
-
-
Cal, P.M.1
Bernardes, G.J.2
Gois, P.M.3
-
34
-
-
84943585335
-
Methods to make homogenous antibody drug conjugates
-
[CrossRef] [PubMed]
-
Kline, T.; Steiner, A.R.; Penta, K.; Sato, A.K.; Hallam, T.J.; Yin, G. Methods to make homogenous antibody drug conjugates. Pharm. Res. 2015, 32, 3480–3493. [CrossRef] [PubMed].
-
(2015)
Pharm. Res
, vol.32
, pp. 3480-3493
-
-
Kline, T.1
Steiner, A.R.2
Penta, K.3
Sato, A.K.4
Hallam, T.J.5
Yin, G.6
-
35
-
-
84902660348
-
Bridging disulfides for stable and defined antibody drug conjugates
-
[CrossRef] [PubMed]
-
Badescu, G.; Bryant, P.; Bird, M.; Henseleit, K.; Swierkosz, J.; Parekh, V.; Tommasi, R.; Pawlisz, E.; Jurlewicz, K.; Farys, M.; et al. Bridging disulfides for stable and defined antibody drug conjugates. Bioconjug. Chem. 2014, 25, 1124–1136. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 1124-1136
-
-
Badescu, G.1
Bryant, P.2
Bird, M.3
Henseleit, K.4
Swierkosz, J.5
Parekh, V.6
Tommasi, R.7
Pawlisz, E.8
Jurlewicz, K.9
Farys, M.10
-
36
-
-
84930652377
-
In vitro and in vivo evaluation of cysteine rebridged trastuzumab-MMAE antibody drug conjugates with defined drug-to-antibody ratios
-
[CrossRef] [PubMed]
-
Bryant, P.; Pabst, M.; Badescu, G.; Bird, M.; McDowell, W.; Jamieson, E.; Swierkosz, J.; Jurlewicz, K.; Tommasi, R.; Henseleit, K.; et al. In vitro and in vivo evaluation of cysteine rebridged trastuzumab-MMAE antibody drug conjugates with defined drug-to-antibody ratios. Mol. Pharm. 2015, 12, 1872–1879. [CrossRef] [PubMed].
-
(2015)
Mol. Pharm
, vol.12
, pp. 1872-1879
-
-
Bryant, P.1
Pabst, M.2
Badescu, G.3
Bird, M.4
McDowell, W.5
Jamieson, E.6
Swierkosz, J.7
Jurlewicz, K.8
Tommasi, R.9
Henseleit, K.10
-
37
-
-
84946567523
-
Antibody_drug conjugates (ADCs) derived from interchain cysteine cross-linking demonstrate improved homogeneity and other pharmacological properties over conventional heterogeneous ADCs
-
[CrossRef] [PubMed]
-
Behrens, C.R.; Ha, E.H.; Chinn, L.L.; Bowers, S.; Probst, G.; Fitch-Bruhns, M.; Monteon, J.; Valdiosera, A.; Bermudez, A.; Liao-Chan, S.; et al. Antibody_drug conjugates (ADCs) derived from interchain cysteine cross-linking demonstrate improved homogeneity and other pharmacological properties over conventional heterogeneous ADCs. Mol. Pharm. 2015, 12, 3986–3998. [CrossRef] [PubMed].
-
(2015)
Mol. Pharm
, vol.12
, pp. 3986-3998
-
-
Behrens, C.R.1
Ha, E.H.2
Chinn, L.L.3
Bowers, S.4
Probst, G.5
Fitch-Bruhns, M.6
Monteon, J.7
Valdiosera, A.8
Bermudez, A.9
Liao-Chan, S.10
-
38
-
-
84951196784
-
Next-generation disulfide stapling: Reduction and functional re-bridging all in one
-
[CrossRef]
-
Lee, M.T.W.; Maruani, A.; Baker, J.R.; Caddick, S.; Chudasama, V. Next-generation disulfide stapling: Reduction and functional re-bridging all in one. Chem. Sci. 2016, 7, 799–802. [CrossRef].
-
(2016)
Chem. Sci
, vol.7
, pp. 799-802
-
-
Lee, M.T.W.1
Maruani, A.2
Baker, J.R.3
Caddick, S.4
Chudasama, V.5
-
39
-
-
84943801701
-
Site-selective multi-porphyrin attachment enables the formation of a next-generation antibody-based photodynamic therapeutic
-
[CrossRef] [PubMed]
-
Maruani, A.; Savoie, H.; Bryden, F.; Caddick, S.; Boyle, R.; Chudasama, V. Site-selective multi-porphyrin attachment enables the formation of a next-generation antibody-based photodynamic therapeutic. Chem. Commun. 2015, 51, 15304–15307. [CrossRef] [PubMed].
-
(2015)
Chem. Commun
, vol.51
, pp. 15304-15307
-
-
Maruani, A.1
Savoie, H.2
Bryden, F.3
Caddick, S.4
Boyle, R.5
Chudasama, V.6
-
40
-
-
84926284885
-
Plug-and-play approach to antibody-based therapeutics via a chemoselective dual click strategy
-
[CrossRef] [PubMed]
-
Maruani, A.; Smith, M.E.B.; Miranda, E.; Chester, K.A.; Chudasama, V.; Caddick, S. A plug-and-play approach to antibody-based therapeutics via a chemoselective dual click strategy. Nat. Commun. 2015, 6, 6645. [CrossRef] [PubMed].
-
(2015)
Nat. Commun
, vol.6
, pp. 6645
-
-
Maruani, A.1
Smith, M.E.B.2
Miranda, E.3
Chester, K.A.4
Chudasama, V.5
Caddick, S.A.6
-
41
-
-
0037399074
-
Directed evolution of O6-alkylguanine-DNA alkyltransferase for efficient labeling of fusion proteins with small molecules in vivo
-
[CrossRef]
-
Juillerat, A.; Gronemeyer, T.; Keppler, A.; Gendreizig, S.; Pick, H.; Vogel, H.; Johnsson, K. Directed evolution of O6-alkylguanine-DNA alkyltransferase for efficient labeling of fusion proteins with small molecules in vivo. Chem. Biol. 2003, 10, 313–317. [CrossRef].
-
(2003)
Chem. Biol
, vol.10
, pp. 313-317
-
-
Juillerat, A.1
Gronemeyer, T.2
Keppler, A.3
Gendreizig, S.4
Pick, H.5
Vogel, H.6
Johnsson, K.7
-
42
-
-
84908102253
-
Development of novel ADCs: Conjugation of tubulysin analogues to trastuzumab monitored by dual radiolabeling
-
[CrossRef] [PubMed]
-
Cohen, R.; Vugts, D.J.; Visser, G.W.M.; Walsum, M.S.-V.; Bolijn, M.; Spiga, M.; Lazzari, P.; Shankar, S.; Sani, M.; Zanda, M.; et al. Development of novel ADCs: Conjugation of tubulysin analogues to trastuzumab monitored by dual radiolabeling. Cancer Res. 2014, 74, 5700–5710. [CrossRef] [PubMed].
-
(2014)
Cancer Res.
, vol.74
, pp. 5700-5710
-
-
Cohen, R.1
Vugts, D.J.2
Visser, G.W.M.3
Walsum, M.S.4
Bolijn, M.5
Spiga, M.6
Lazzari, P.7
Shankar, S.8
Sani, M.9
Zanda, M.10
-
43
-
-
0023823192
-
Determination of the number of e-amino groups available for conjugation of effect or molecules to monoclonal antibodies
-
[CrossRef] [PubMed]
-
Mueller, B.M.; Wrasidlo, W.A.; Reisfeld, R.A. Determination of the number of e-amino groups available for conjugation of effect or molecules to monoclonal antibodies. Hybridoma 1988, 7, 453–456. [CrossRef] [PubMed].
-
(1988)
Hybridoma
, vol.7
, pp. 453-456
-
-
Mueller, B.M.1
Wrasidlo, W.A.2
Reisfeld, R.A.3
-
44
-
-
77956637683
-
Physicochemical stability of the antibody-drug conjugate Trastuzumab-DM1: Changes due to modification and conjugation processes
-
[CrossRef] [PubMed]
-
Wakankar, A.A.; Feeney, M.B.; Rivera, J.; Chen, Y.; Kim, M.; Sharma, V.K.; Wang, Y.J. Physicochemical stability of the antibody-drug conjugate Trastuzumab-DM1: Changes due to modification and conjugation processes. Bioconjug. Chem. 2010, 21, 1588–1595. [CrossRef] [PubMed].
-
(2010)
Bioconjug. Chem.
, vol.21
, pp. 1588-1595
-
-
Wakankar, A.A.1
Feeney, M.B.2
Rivera, J.3
Chen, Y.4
Kim, M.5
Sharma, V.K.6
Wang, Y.J.7
-
45
-
-
0030805884
-
Calicheamicin derivatives conjugated to monoclonal antibodies: Determination of loading values and distributions by infrared and UV matrix-assisted laser desorption/ionization mass spectrometry and electrospray ionization mass spectrometry
-
[CrossRef]
-
Siegel, M.M.; Tabei, K.; Kunz, A.; Hollander, I.J.; Hamann, R.R.; Bell, D.H.; Berkenkamp, S.; Hillenkamp, F. Calicheamicin derivatives conjugated to monoclonal antibodies: Determination of loading values and distributions by infrared and UV matrix-assisted laser desorption/ionization mass spectrometry and electrospray ionization mass spectrometry. Anal. Chem. 1997, 69, 2716–2726. [CrossRef].
-
(1997)
Anal. Chem
, vol.69
, pp. 2716-2726
-
-
Siegel, M.M.1
Tabei, K.2
Kunz, A.3
Hollander, I.J.4
Hamann, R.R.5
Bell, D.H.6
Berkenkamp, S.7
Hillenkamp, F.8
-
46
-
-
0033893747
-
Region-selective labeling of antibodies as determined by electrospray ionization-mass spectrometry (ESI-MS)
-
[CrossRef]
-
Adamczyk, M.; Gebler, J.; Shreder, K.; Wu, J. Region-selective labeling of antibodies as determined by electrospray ionization-mass spectrometry (ESI-MS). Bioconjug. Chem. 2000, 11, 557–563. [CrossRef].
-
(2000)
Bioconjug. Chem
, vol.11
, pp. 557-563
-
-
Adamczyk, M.1
Gebler, J.2
Shreder, K.3
Wu, J.4
-
47
-
-
0036007596
-
Gemtuzumab ozogamicin, a potent and selective anti-CD33 antibody-calicheamicin conjugate for treatment of acute myeloid leukemia
-
[CrossRef] [PubMed]
-
Hamann, P.R.; Hinman, L.M.; Hollander, I.; Beyer, C.F.; Lindh, D.; Holcomb, R.; Hallett, W.; Tsou, H.R.; Upeslacis, J.; Shochat, D.; et al. Gemtuzumab ozogamicin, a potent and selective anti-CD33 antibody-calicheamicin conjugate for treatment of acute myeloid leukemia. Bioconjug. Chem. 2002, 13, 47–58. [CrossRef] [PubMed].
-
(2002)
Bioconjug. Chem
, vol.13
, pp. 47-58
-
-
Hamann, P.R.1
Hinman, L.M.2
Hollander, I.3
Beyer, C.F.4
Lindh, D.5
Holcomb, R.6
Hallett, W.7
Tsou, H.R.8
Upeslacis, J.9
Shochat, D.10
-
48
-
-
84938751906
-
Conjugates of small molecule drugs with antibodies and other proteins
-
[CrossRef]
-
Feng, Y.; Zhu, Z.; Chen, W.; Prabakaran, P.; Lin, K.; Dimitrov, D. Conjugates of small molecule drugs with antibodies and other proteins. Biomedicines 2014, 2, 1–13. [CrossRef].
-
(2014)
Biomedicines
, vol.2
, pp. 1-13
-
-
Feng, Y.1
Zhu, Z.2
Chen, W.3
Prabakaran, P.4
Lin, K.5
Dimitrov, D.6
-
49
-
-
79960092388
-
Cancer-targeting antibody-drug con jugates:Site-specific conjugation of doxorubicin to anti-EGFR 528 Fab9 through a polyethylene glycol linker. Aust
-
[CrossRef]
-
Hong, L.P.T.; Scoble, J.A.; Doughty, L.; Coia, G.; Williams, C.C. Cancer-targeting antibody-drug con jugates:Site-specific conjugation of doxorubicin to anti-EGFR 528 Fab9 through a polyethylene glycol linker. Aust. J. Chem. 2011, 64, 779–789. [CrossRef].
-
(2011)
J. Chem
, vol.64
, pp. 779-789
-
-
Hong, L.P.T.1
Scoble, J.A.2
Doughty, L.3
Coia, G.4
Williams, C.C.5
-
50
-
-
78650297318
-
Site-specific and stoichiometric modification of antibodies by bacterial transglutaminase
-
[CrossRef] [PubMed]
-
Jeger, S.; Zimmermann, K.; Blanc, A.; Grünberg, J.; Honer, M.; Hunziker, P.; Struthers, H.; Schibli, R. Site-specific and stoichiometric modification of antibodies by bacterial transglutaminase. Angew. Chem. Int. Ed. Engl. 2010, 49, 9995–9997. [CrossRef] [PubMed].
-
(2010)
Angew. Chem. Int. Ed. Engl
, vol.49
, pp. 9995-9997
-
-
Jeger, S.1
Zimmermann, K.2
Blanc, A.3
Grünberg, J.4
Honer, M.5
Hunziker, P.6
Struthers, H.7
Schibli, R.8
-
51
-
-
0033618622
-
Staphylococcus aureus sortase, an enzyme that anchors surface proteins to the cell wall
-
[CrossRef] [PubMed]
-
Mazmanian, S.K.; Liu, G.; Ton-That, H.; Schneewind, O. Staphylococcus aureus sortase, an enzyme that anchors surface proteins to the cell wall. Science 1999, 285, 760–763. [CrossRef] [PubMed].
-
(1999)
Science
, vol.285
, pp. 760-763
-
-
Mazmanian, S.K.1
Liu, G.2
Ton-That, H.3
Schneewind, O.4
-
52
-
-
65549164210
-
Sortase-mediated ligation: A gift from Gram-positive bacteria to protein engineering
-
[CrossRef] [PubMed]
-
Tsukiji, S.; Nagamune, T. Sortase-mediated ligation: A gift from Gram-positive bacteria to protein engineering. Chem. Biochem. Eur. J. Chem. Biol. 2009, 10, 787–798. [CrossRef] [PubMed].
-
(2009)
Chem. Biochem. Eur. J. Chem. Biol
, vol.10
, pp. 787-798
-
-
Tsukiji, S.1
Nagamune, T.2
-
53
-
-
84859891859
-
Engineering of an anti-epidermal growth factor receptor antibody to single chain format and labeling by Sortase A-mediated protein ligation
-
[CrossRef] [PubMed]
-
Madej, M.P.; Coia, G.; Williams, C.C.; Caine, J.M.; Pearce, L.A.; Attwood, R.; Bartone, N.A.; Dolezal, O.; Nisbet, R.M.; Nuttall, S.D.; et al. Engineering of an anti-epidermal growth factor receptor antibody to single chain format and labeling by Sortase A-mediated protein ligation. Biotechnol. Bioeng. 2012, 109, 1461–1470. [CrossRef] [PubMed].
-
(2012)
Biotechnol. Bioeng
, vol.109
, pp. 1461-1470
-
-
Madej, M.P.1
Coia, G.2
Williams, C.C.3
Caine, J.M.4
Pearce, L.A.5
Attwood, R.6
Bartone, N.A.7
Dolezal, O.8
Nisbet, R.M.9
Nuttall, S.D.10
-
54
-
-
84866928403
-
Enzymatic antibody tagging: Toward a universal biocompatible targeting tool
-
[CrossRef] [PubMed]
-
Ta, H.T.; Peter, K.; Hagemeyer, C.E. Enzymatic antibody tagging: Toward a universal biocompatible targeting tool. Trends Cardiovasc. Med. 2012, 22, 105–111. [CrossRef] [PubMed].
-
(2012)
Trends Cardiovasc. Med
, vol.22
, pp. 105-111
-
-
Ta, H.T.1
Peter, K.2
Hagemeyer, C.E.3
-
55
-
-
84883180740
-
Efficient N-terminal labeling of proteins by use of sortase
-
[CrossRef]
-
Williamson, D.J.; Fascione, M.A.; Webb, M.E.; Turnbull, W.B. Efficient N-terminal labeling of proteins by use of sortase. Angew. Chem. 2012, 124, 9511–9514. [CrossRef].
-
(2012)
Angew. Chem
, vol.124
, pp. 9511-9514
-
-
Williamson, D.J.1
Fascione, M.A.2
Webb, M.E.3
Turnbull, W.B.4
-
56
-
-
18744401100
-
Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase
-
[CrossRef] [PubMed]
-
Chen, I.; Howarth, M.; Lin, W.; Ting, A.Y. Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase. Nat. Methods 2005, 2, 99–104. [CrossRef] [PubMed].
-
(2005)
Nat. Methods
, vol.2
, pp. 99-104
-
-
Chen, I.1
Howarth, M.2
Lin, W.3
Ting, A.Y.4
-
57
-
-
20144367846
-
Design, synthesis, and in vitro evaluation of dipeptide-based antibody minor groove binder conjugates
-
[CrossRef] [PubMed]
-
Jeffrey, S.C.; Torgov, M.Y.; Andreyka, J.B.; Boddington, L.; Cerveny, C.G.; Denny, W.A.; Gordon, K.A.; Gustin, D.; Haugen, J.; Toni Kline, T.; et al. Design, synthesis, and in vitro evaluation of dipeptide-based antibody minor groove binder conjugates. J. Med. Chem. 2005, 48, 1344–1358. [CrossRef] [PubMed].
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1344-1358
-
-
Jeffrey, S.C.1
Torgov, M.Y.2
Andreyka, J.B.3
Boddington, L.4
Cerveny, C.G.5
Denny, W.A.6
Gordon, K.A.7
Gustin, D.8
Haugen, J.9
Toni Kline, T.10
-
58
-
-
67649215051
-
Design, synthesis, and biological evaluation of antibody-drug conjugates comprised of potent camptothecin analogues
-
[CrossRef] [PubMed]
-
Burke, P.J.; Senter, P.D.; Meyer, D.W.; Miyamoto, J.B.; Anderson, M.; Toki, B.E.; Manikumar, G.; Wani, M.C.; Kroll, D.J.; Jeffrey, S.C. Design, synthesis, and biological evaluation of antibody-drug conjugates comprised of potent camptothecin analogues. Bioconjug. Chem. 2009, 20, 1242–1250. [CrossRef] [PubMed].
-
(2009)
Bioconjug. Chem
, vol.20
, pp. 1242-1250
-
-
Burke, P.J.1
Senter, P.D.2
Meyer, D.W.3
Miyamoto, J.B.4
Anderson, M.5
Toki, B.E.6
Manikumar, G.7
Wani, M.C.8
Kroll, D.J.9
Jeffrey, S.C.10
-
59
-
-
0036074253
-
Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: Model studies of enzymatic drug release and antigen-specific in vitro anticancer activity
-
[CrossRef] [PubMed]
-
Dubowchik, G.M.; Firestone, R.A.; Padilla, L.; Willner, D.; Hofstead, S.J.; Mosure, K.; Knipe, J.O.; Lasch, S.J.; Trail, P.A. Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: Model studies of enzymatic drug release and antigen-specific in vitro anticancer activity. Bioconjug. Chem. 2002, 13, 855–869. [CrossRef] [PubMed].
-
(2002)
Bioconjug. Chem
, vol.13
, pp. 855-869
-
-
Dubowchik, G.M.1
Firestone, R.A.2
Padilla, L.3
Willner, D.4
Hofstead, S.J.5
Mosure, K.6
Knipe, J.O.7
Lasch, S.J.8
Trail, P.A.9
-
60
-
-
0037068501
-
Monoclonal antibody conjugates of doxorubicin prepared with branched peptide linkers: Inhibition of aggregation by methoxytriethyleneglycol chains
-
[CrossRef] [PubMed]
-
King, H.D.; Dubowchik, G.M.; Mastalerz, H.; Willner, D.; Hofstead, S.J.; Firestone, R.A.; Lasch, S.J.; Trail, P.A. Monoclonal antibody conjugates of doxorubicin prepared with branched peptide linkers: Inhibition of aggregation by methoxytriethyleneglycol chains. J. Med. Chem. 2002, 45, 4336–4343. [CrossRef] [PubMed].
-
(2002)
J. Med. Chem
, vol.45
, pp. 4336-4343
-
-
King, H.D.1
Dubowchik, G.M.2
Mastalerz, H.3
Willner, D.4
Hofstead, S.J.5
Firestone, R.A.6
Lasch, S.J.7
Trail, P.A.8
-
61
-
-
0037147785
-
Synthesis of an immunoconjugate of camptothecin
-
[CrossRef]
-
Walker, M.A.; Dubowchik, G.M.; Hofstead, S.J.; Trail, P.A.; Firestone, R.A. Synthesis of an immunoconjugate of camptothecin. Bioorg. Med. Chem. Lett. 2002, 12, 217–219. [CrossRef].
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 217-219
-
-
Walker, M.A.1
Dubowchik, G.M.2
Hofstead, S.J.3
Trail, P.A.4
Firestone, R.A.5
-
62
-
-
84930626816
-
Design, synthesis, and evaluation of linker-duocarmycin payloads: Toward selection of HER2-targeting antibody_drug conjugate SYD985
-
[CrossRef]
-
Elgersma, R.C.; Coumans, R.G.E.; Huijbregts, T.; Menge, W.M.P.B.; Joosten, J.A.F.; Spijker, H.J.; de Groot, F.M.H.; van der Lee, M.M.C.; Ubink, R.; van den Dobbelsteen, D.J. Design, synthesis, and evaluation of linker-duocarmycin payloads: Toward selection of HER2-targeting antibody_drug conjugate SYD985. Mol. Pharm. 2015, 12, 1813–1835. [CrossRef].
-
(2015)
Mol. Pharm.
, vol.12
, pp. 1813-1835
-
-
Elgersma, R.C.1
Coumans, R.G.E.2
Huijbregts, T.3
Menge, W.M.P.B.4
Joosten, J.A.F.5
Spijker, H.J.6
De Groot, F.M.H.7
Van Der Lee, M.M.C.8
Ubink, R.9
Dobbelsteen, V.D.10
-
63
-
-
56249091442
-
Antibody conjugates of 7-ethyl-10-hydroxycamptothecin (SN-38) for targeted cancer chemotherapy
-
[CrossRef] [PubMed]
-
Moon, S.-J.; Govindan, S.V.; Cardillo, T.M.; D’Souza, C.A.; Hansen, H.J.; Goldenberg, D.M. Antibody conjugates of 7-ethyl-10-hydroxycamptothecin (SN-38) for targeted cancer chemotherapy. J. Med. Chem. 2008, 51, 6916–6926. [CrossRef] [PubMed].
-
(2008)
J. Med. Chem
, vol.51
, pp. 6916-6926
-
-
Moon, S.-J.1
Govindan, S.V.2
Cardillo, T.M.3
D’Souza, C.A.4
Hansen, H.J.5
Goldenberg, D.M.6
-
64
-
-
42949130549
-
Novel prodrugs of SN-38 using multiarm poly(Ethylene glycol) linkers
-
[CrossRef] [PubMed]
-
Zhao, H.; Rubio, B.; Sapra, P.; Wu, D.; Reddy, P.; Sai, P.; Martinez, A.; Gao, Y.; Lozanguiez, Y.; Longley, C.; et al. Novel prodrugs of SN-38 using multiarm poly(ethylene glycol) linkers. Bioconjug. Chem. 2008, 19, 849–859. [CrossRef] [PubMed].
-
(2008)
Bioconjug. Chem.
, vol.19
, pp. 849-859
-
-
Zhao, H.1
Rubio, B.2
Sapra, P.3
Wu, D.4
Reddy, P.5
Sai, P.6
Martinez, A.7
Gao, Y.8
Lozanguiez, Y.9
Longley, C.10
-
65
-
-
0037155531
-
Protease mediated fragmentation of p-amidobenzyl ethers: A new strategy for the activation of anticancer prodrugs
-
[CrossRef]
-
Toki, B.E.; Cerveny, C.G.; Wahl, A.F.; Senter, P.D. Protease mediated fragmentation of p-amidobenzyl ethers: A new strategy for the activation of anticancer prodrugs. J. Org. Chem. 2002, 67, 1866–1872. [CrossRef].
-
(2002)
J. Org. Chem
, vol.67
, pp. 1866-1872
-
-
Toki, B.E.1
Cerveny, C.G.2
Wahl, A.F.3
Senter, P.D.4
-
66
-
-
0035046645
-
DNA minor groove alkylating agents
-
[CrossRef] [PubMed]
-
Denny, W.A. DNA minor groove alkylating agents. Curr. Med. Chem. 2001, 8, 533–544. [CrossRef] [PubMed].
-
(2001)
Curr. Med. Chem
, vol.8
, pp. 533-544
-
-
Denny, W.A.1
-
67
-
-
77249172711
-
Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy
-
[CrossRef] [PubMed]
-
Quiles, S.; Raisch, K.P.; Sanford, L.L.; Bonner, J.A.; Safavy, A. Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy. J. Med. Chem. 2010, 53, 586–594. [CrossRef] [PubMed].
-
(2010)
J. Med. Chem
, vol.53
, pp. 586-594
-
-
Quiles, S.1
Raisch, K.P.2
Sanford, L.L.3
Bonner, J.A.4
Safavy, A.5
-
68
-
-
84904408813
-
Aldehyde tag coupled with HIPS chemistry enables the production of ADCs conjugated site-specifically to different antibody regions with distinct in vivo efficacy and PK outcomes
-
[CrossRef]
-
Drake, P.M.; Albers, A.E.; Baker, J.; Banas, S.; Barfield, R.M.; Bhat, A.S.; de Hart, G.W.; Garofalo, A.W.; Holder, P. Aldehyde tag coupled with HIPS chemistry enables the production of ADCs conjugated site-specifically to different antibody regions with distinct in vivo efficacy and PK outcomes. Bioconjug. Chem. 2014, 25, 1331–1341. [CrossRef].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 1331-1341
-
-
Drake, P.M.1
Albers, A.E.2
Baker, J.3
Banas, S.4
Barfield, R.M.5
Bhat, A.S.6
De Hart, G.W.7
Garofalo, A.W.8
Holder, P.9
-
69
-
-
84861034877
-
Site-specific chemical protein conjugation using genetically encoded aldehyde tags
-
[CrossRef]
-
Rabuka, D.; Rush, J.S.; de Hart, G.W.; Wu, P.; Bertozzi, C.R. Site-specific chemical protein conjugation using genetically encoded aldehyde tags. Nat. Protoc. 2012, 7, 1052–1067. [CrossRef].
-
(2012)
Nat. Protoc
, vol.7
, pp. 1052-1067
-
-
Rabuka, D.1
Rush, J.S.2
De Hart, G.W.3
Wu, P.4
Bertozzi, C.R.5
-
70
-
-
84879340492
-
Hydrazino-Pictet-Spengler ligation as a biocompatible method for the generation of stable protein conjugates
-
[CrossRef]
-
Agarwal, P.; Kudirka, R.; Albers, A.E.; Barfield, R.M.; de Hart, G.W.; Drake, P.M.; Jones, L.C.; Rabuka, D. Hydrazino-Pictet-Spengler ligation as a biocompatible method for the generation of stable protein conjugates. Bioconjug. Chem. 2013, 24, 846–851. [CrossRef].
-
(2013)
Bioconjug. Chem
, vol.24
, pp. 846-851
-
-
Agarwal, P.1
Kudirka, R.2
Albers, A.E.3
Barfield, R.M.4
De Hart, G.W.5
Drake, P.M.6
Jones, L.C.7
Rabuka, D.8
-
71
-
-
84906055556
-
The exploding genetic code
-
[CrossRef] [PubMed]
-
Lemke, E.A. The exploding genetic code. ChemBioChem 2014, 15, 1691–1694. [CrossRef] [PubMed].
-
(2014)
Chembiochem
, vol.15
, pp. 1691-1694
-
-
Lemke, E.A.1
-
72
-
-
84878842686
-
Protein conjugation with genetically encoded unnatural amino acids
-
[CrossRef] [PubMed]
-
Kim, C.H.; Axup, J.Y.; Schultz, P.G. Protein conjugation with genetically encoded unnatural amino acids. Curr. Opin. Chem. Biol. 2013, 17, 412–419. [CrossRef] [PubMed].
-
(2013)
Curr. Opin. Chem. Biol
, vol.17
, pp. 412-419
-
-
Kim, C.H.1
Axup, J.Y.2
Schultz, P.G.3
-
73
-
-
79953052077
-
Selective formation of covalent protein heterodimers with an unnatural amino acid
-
[CrossRef] [PubMed]
-
Hutchins, B.M.; Kazane, S.A.; Staflin, K.; Forsyth, J.S.; Felding-Habermann, B.; Smider, V.V.; Schultz, P.G. Selective formation of covalent protein heterodimers with an unnatural amino acid. Chem. Biol. 2011, 18, 299–303. [CrossRef] [PubMed].
-
(2011)
Chem. Biol
, vol.18
, pp. 299-303
-
-
Hutchins, B.M.1
Kazane, S.A.2
Staflin, K.3
Forsyth, J.S.4
Felding-Habermann, B.5
Smider, V.V.6
Schultz, P.G.7
-
74
-
-
84867040452
-
Synthesis of site-specific antibody–drug conjugates using unnatural amino acids
-
[CrossRef] [PubMed]
-
Axup, J.Y.; Bajjuri, K.M.; Ritland, M.; Hutchins, B.M.; Kim, C.H.; Kazane, S.A.; Halder, R.; Forsyth, J.S.; Santidrian, A.F. Synthesis of site-specific antibody–drug conjugates using unnatural amino acids. Proc. Natl. Acad. Sci. USA 2012, 109, 16101–16106. [CrossRef] [PubMed].
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 16101-16106
-
-
Axup, J.Y.1
Bajjuri, K.M.2
Ritland, M.3
Hutchins, B.M.4
Kim, C.H.5
Kazane, S.A.6
Halder, R.7
Forsyth, J.S.8
Santidrian, A.F.9
-
75
-
-
84896537748
-
Site-specific antibody–drug conjugation through glycoengineering
-
[CrossRef]
-
Zhou, Q.; Stefano, J.E.; Manning, C.; Kyazike, J.; Chen, B.; Gianolio, D.A.; Park, A.; Busch, M.; Bird, J. Site-specific antibody–drug conjugation through glycoengineering. Bioconjug. Chem. 2014, 25, 510–520. [CrossRef].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 510-520
-
-
Zhou, Q.1
Stefano, J.E.2
Manning, C.3
Kyazike, J.4
Chen, B.5
Gianolio, D.A.6
Park, A.7
Busch, M.8
Bird, J.9
-
76
-
-
84875213206
-
Site-Specific protein bioconjugation via a pyridoxal 51-phosphate-mediated N-terminal transamination reaction
-
[PubMed]
-
Witus, L.S.; Francis, M. Site-Specific protein bioconjugation via a pyridoxal 51-phosphate-mediated N-terminal transamination reaction. Curr. Protoc. Chem. Biol. 2010, 2, 125–134. [PubMed].
-
(2010)
Curr. Protoc. Chem. Biol
, vol.2
, pp. 125-134
-
-
Witus, L.S.1
Francis, M.2
-
77
-
-
54749084565
-
Hydrolytic stability of hydrazones and oximes
-
[CrossRef] [PubMed]
-
Kalia, J.; Raines, R.T. Hydrolytic stability of hydrazones and oximes. Angew. Chem. Int. Ed. 2008, 47, 7523–7526. [CrossRef] [PubMed].
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 7523-7526
-
-
Kalia, J.1
Raines, R.T.2
-
78
-
-
33845555256
-
Mild and simple biomimetic conversion of amines to carbonyl compounds
-
[CrossRef]
-
Buckley, T.F.; Rapoport, H. Mild and simple biomimetic conversion of amines to carbonyl compounds. J. Am. Chem. Soc. 1982, 104, 4446–4450. [CrossRef].
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 4446-4450
-
-
Buckley, T.F.1
Rapoport, H.2
-
79
-
-
84887810619
-
Site-Specific Protein Transamination Using N-Methylpyridinium-4-Carboxaldehyde
-
[CrossRef] [PubMed]
-
Witus, L.S.; Netirojjanakul, C.; Palla, K.S.; Muehl, E. M.; Weng, C.-H.; Iavarone, A.T.; Francis, M.B. Site-Specific Protein Transamination Using N-Methylpyridinium-4-Carboxaldehyde. J. Am. Chem. Soc. 2013, 135, 17223–17229. [CrossRef] [PubMed].
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 17223-17229
-
-
Witus, L.S.1
Netirojjanakul, C.2
Palla, K.S.3
Muehl, E.M.4
Weng, C.-H.5
Iavarone, A.T.6
Francis, M.B.7
-
80
-
-
84902668734
-
Parallel Synthesis and screening of peptide conjugates
-
[CrossRef] [PubMed]
-
Dirksen, A.; Madsen, M.; Iacono, G.D.; Matin, M.J.; Bacica, M.; Stankovic, N.; Callans, S.; Bhat, A. Parallel Synthesis and screening of peptide conjugates. Bioconjug. Chem. 2014, 25, 1052–1060. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem.
, vol.25
, pp. 1052-1060
-
-
Dirksen, A.1
Madsen, M.2
Iacono, G.D.3
Matin, M.J.4
Bacica, M.5
Stankovic, N.6
Callans, S.7
Bhat, A.8
-
81
-
-
84883673308
-
Bioconjugation by native chemical tagging of C–H bonds
-
[CrossRef] [PubMed]
-
Zhou, Q.; Gui, J.; Pan, C.-M.; Albone, E.; Cheng, X.; Suh, E.M.; Grasso, L.; Ishihara, Y.; Baran, P.S. Bioconjugation by native chemical tagging of C–H bonds. J. Am. Chem. Soc. 2013, 135, 12994–12997. [CrossRef] [PubMed].
-
(2013)
J. Am. Chem. Soc
, vol.135
, pp. 12994-12997
-
-
Zhou, Q.1
Gui, J.2
Pan, C.-M.3
Albone, E.4
Cheng, X.5
Suh, E.M.6
Grasso, L.7
Ishihara, Y.8
Baran, P.S.9
-
82
-
-
0036901574
-
Transglutaminases: Nature’s biological glues
-
[CrossRef] [PubMed]
-
Griffin, M.; Casadio, R.; Bergamini, C.M. Transglutaminases: Nature’s biological glues. Biochem. J. 2002, 396, 377–396. [CrossRef] [PubMed].
-
(2002)
Biochem. J.
, vol.396
, pp. 377-396
-
-
Griffin, M.1
Casadio, R.2
Bergamini, C.M.3
-
83
-
-
84896530100
-
Transglutaminase-based chemo-enzymatic conjugation approach yields homogeneous antibody–drug conjugates
-
[CrossRef] [PubMed]
-
Dennler, P.; Chiotellis, A.; Fischer, E.; Brégeon, D.; Belmant, C.; Gauthier, L.; Lhospice, F.; Romagne, F.; Schibli, R. Transglutaminase-based chemo-enzymatic conjugation approach yields homogeneous antibody–drug conjugates. Bioconjug. Chem. 2014, 25, 569–578. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 569-578
-
-
Dennler, P.1
Chiotellis, A.2
Fischer, E.3
Brégeon, D.4
Belmant, C.5
Gauthier, L.6
Lhospice, F.7
Romagne, F.8
Schibli, R.9
-
84
-
-
84901052647
-
Versatility of microbial transglutaminase
-
[CrossRef] [PubMed]
-
Strop, P. Versatility of microbial transglutaminase. Bioconjug. Chem. 2014, 25, 855–862. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 855-862
-
-
Strop, P.1
-
85
-
-
84874300889
-
Location matters: Site of conjugation modulates stability and pharmacokinetics of antibody drug conjugates
-
[CrossRef] [PubMed]
-
Strop, P.; Liu, S.H.; Dorywalska, M.; Delaria, K.; Dushin, R.G.; Tran, T.T.; Ho, W.H.; Farias, S.; Casas, M.G.; Abdiche, Y.; et al. Location matters: Site of conjugation modulates stability and pharmacokinetics of antibody drug conjugates. Chem. Biol. 2013, 20, 161–167. [CrossRef] [PubMed].
-
(2013)
Chem. Biol.
, vol.20
, pp. 161-167
-
-
Strop, P.1
Liu, S.H.2
Dorywalska, M.3
Delaria, K.4
Dushin, R.G.5
Tran, T.T.6
Ho, W.H.7
Farias, S.8
Casas, M.G.9
Abdiche, Y.10
-
86
-
-
84894445908
-
Production of site-specific antibody–drug conjugates using optimized non-natural amino acids in a cell-free expression system
-
[CrossRef] [PubMed]
-
Zimmerman, E.S.; Heibeck, T.H.; Gill, A.; Li, X.; Murray, C.J.; Madlansacay, M.R.; Tran, C.; Uter, N.T.; Yin, G.; Rivers, P.J. Production of site-specific antibody–drug conjugates using optimized non-natural amino acids in a cell-free expression system. Bioconjug. Chem. 2014, 25, 351–361. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 351-361
-
-
Zimmerman, E.S.1
Heibeck, T.H.2
Gill, A.3
Li, X.4
Murray, C.J.5
Madlansacay, M.R.6
Tran, C.7
Uter, N.T.8
Yin, G.9
Rivers, P.J.10
-
87
-
-
84896500653
-
Regioselective and stoichiometrically controlled conjugation of photodynamic sensitizers to a HER2 targeting antibody fragment
-
[CrossRef] [PubMed]
-
Bryden, F.; Maruani, A.; Savoie, H.; Chudasama, V.; Smith, M.E.B.; Caddick, S.; Boyle, R.W. Regioselective and stoichiometrically controlled conjugation of photodynamic sensitizers to a HER2 targeting antibody fragment. Bioconjug. Chem. 2014, 25, 611–617. [CrossRef] [PubMed].
-
(2014)
Bioconjug. Chem
, vol.25
, pp. 611-617
-
-
Bryden, F.1
Maruani, A.2
Savoie, H.3
Chudasama, V.4
Smith, M.E.B.5
Caddick, S.6
Boyle, R.W.7
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