메뉴 건너뛰기




Volumn 27, Issue 5, 2016, Pages 1324-1331

One-Step Conjugation Method for Site-Specific Antibody-Drug Conjugates through Reactive Cysteine-Engineered Antibodies

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ANTIBODIES; CELL ENGINEERING; HYDROLYSIS; PLASMA STABILITY; SULFUR COMPOUNDS;

EID: 84971251113     PISSN: 10431802     EISSN: 15204812     Source Type: Journal    
DOI: 10.1021/acs.bioconjchem.6b00133     Document Type: Article
Times cited : (53)

References (32)
  • 1
    • 84877310777 scopus 로고    scopus 로고
    • Maturing antibody-drug conjugate pipeline hits 30
    • Mullard, A. (2013) Maturing antibody-drug conjugate pipeline hits 30 Nat. Rev. Drug Discovery 12, 329-32 10.1038/nrd4009
    • (2013) Nat. Rev. Drug Discovery , vol.12 , pp. 329-332
    • Mullard, A.1
  • 2
    • 84898066972 scopus 로고    scopus 로고
    • Antibody-drug conjugates: An emerging concept in cancer therapy
    • Chari, R. V., Miller, M. L., and Widdison, W. C. (2014) Antibody-drug conjugates: an emerging concept in cancer therapy Angew. Chem., Int. Ed. 53, 3796-827 10.1002/anie.201307628
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 3796-3827
    • Chari, R.V.1    Miller, M.L.2    Widdison, W.C.3
  • 4
    • 84923228905 scopus 로고    scopus 로고
    • Site-specific antibody-drug conjugates: The nexus of bioorthogonal chemistry, protein engineering, and drug development
    • Agarwal, P. and Bertozzi, C. R. (2015) Site-specific antibody-drug conjugates: the nexus of bioorthogonal chemistry, protein engineering, and drug development Bioconjugate Chem. 26, 176-92 10.1021/bc5004982
    • (2015) Bioconjugate Chem. , vol.26 , pp. 176-192
    • Agarwal, P.1    Bertozzi, C.R.2
  • 11
    • 84903715027 scopus 로고    scopus 로고
    • Preparation of well-defined antibody-drug conjugates through glycan remodeling and strain-promoted azide-alkyne cycloadditions
    • Li, X., Fang, T., and Boons, G. J. (2014) Preparation of well-defined antibody-drug conjugates through glycan remodeling and strain-promoted azide-alkyne cycloadditions Angew. Chem., Int. Ed. 53, 7179-82 10.1002/anie.201402606
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 7179-7182
    • Li, X.1    Fang, T.2    Boons, G.J.3
  • 14
    • 84904408813 scopus 로고    scopus 로고
    • 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
    • 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., and Jones, L. C. et al. 2014, 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 Bioconjugate Chem. 25, 1331-41 10.1021/bc500189z
    • (2014) Bioconjugate 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    Jones, L.C.10
  • 17
    • 84934988904 scopus 로고    scopus 로고
    • Identification of highly reactive cysteine residues at less exposed positions in the Fab constant region for site-specific conjugation
    • Shiraishi, Y., Muramoto, T., Nagatomo, K., Shinmi, D., Honma, E., Masuda, K., and Yamasaki, M. (2015) Identification of highly reactive cysteine residues at less exposed positions in the Fab constant region for site-specific conjugation Bioconjugate Chem. 26, 1032-40 10.1021/acs.bioconjchem.5b00080
    • (2015) Bioconjugate Chem. , vol.26 , pp. 1032-1040
    • Shiraishi, Y.1    Muramoto, T.2    Nagatomo, K.3    Shinmi, D.4    Honma, E.5    Masuda, K.6    Yamasaki, M.7
  • 18
    • 84941317860 scopus 로고    scopus 로고
    • Antibody-drug conjugates for cancer therapy: The technological and regulatory challenges of developing drug-biologic hybrids
    • Hamilton, G. S. (2015) Antibody-drug conjugates for cancer therapy: The technological and regulatory challenges of developing drug-biologic hybrids Biologicals 43, 318-32 10.1016/j.biologicals.2015.05.006
    • (2015) Biologicals , vol.43 , pp. 318-332
    • Hamilton, G.S.1
  • 19
    • 84934438721 scopus 로고    scopus 로고
    • Engineering THIOMABs for Site-Specific Conjugation of Thiol-Reactive Linkers
    • In (Ducry, L. Ed.) pp, Springer, New York
    • Bhakta, S., Raab, H., and Junutula, J. R. (2013) Engineering THIOMABs for Site-Specific Conjugation of Thiol-Reactive Linkers. In Methods in Molecular Biology. Vol. 1045: Antibody-Drug Conjugtes (Ducry, L., Ed.) pp 189-204, Springer, New York.
    • (2013) Methods in Molecular Biology. Vol. 1045: Antibody-Drug Conjugtes , pp. 189-204
    • Bhakta, S.1    Raab, H.2    Junutula, J.R.3
  • 20
    • 80054828086 scopus 로고    scopus 로고
    • Tunable degradation of maleimide-thiol adducts in reducing environments
    • Baldwin, A. D. and Kiick, K. L. (2011) Tunable degradation of maleimide-thiol adducts in reducing environments Bioconjugate Chem. 22, 1946-53 10.1021/bc200148v
    • (2011) Bioconjugate Chem. , vol.22 , pp. 1946-1953
    • Baldwin, A.D.1    Kiick, K.L.2
  • 24
    • 84898005371 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of cysteine and site specific conjugated herceptin antibody-drug conjugates
    • Jackson, D., Atkinson, J., Guevara, C. I., Zhang, C., Kery, V., Moon, S. J., Virata, C., Yang, P., Lowe, C., and Pinkstaff, J. et al. 2014, In vitro and in vivo evaluation of cysteine and site specific conjugated herceptin antibody-drug conjugates PLoS One 9, e83865 10.1371/journal.pone.0083865
    • (2014) PLoS One , vol.9 , pp. e83865
    • Jackson, D.1    Atkinson, J.2    Guevara, C.I.3    Zhang, C.4    Kery, V.5    Moon, S.J.6    Virata, C.7    Yang, P.8    Lowe, C.9    Pinkstaff, J.10
  • 25
    • 84946567523 scopus 로고    scopus 로고
    • Antibody-Drug Conjugates (ADCs) Derived from Interchain Cysteine Cross-Linking Demonstrate Improved Homogeneity and Other Pharmacological Properties over Conventional Heterogeneous ADCs
    • Behrens, C. R., Ha, E. H., Chinn, L. L., Bowers, S., Probst, G., Fitch-Bruhns, M., Monteon, J., Valdiosera, A., Bermudez, A., and Liao-Chan, S. et al. 2015, Antibody-Drug Conjugates (ADCs) Derived from Interchain Cysteine Cross-Linking Demonstrate Improved Homogeneity and Other Pharmacological Properties over Conventional Heterogeneous ADCs Mol. Pharmaceutics 12, 3986-98 10.1021/acs.molpharmaceut.5b00432
    • (2015) Mol. Pharmaceutics , 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
  • 28
    • 84884551591 scopus 로고    scopus 로고
    • The thiol pool in human plasma: The central contribution of albumin to redox processes
    • Turell, L., Radi, R., and Alvarez, B. (2013) The thiol pool in human plasma: the central contribution of albumin to redox processes Free Radical Biol. Med. 65, 244-53 10.1016/j.freeradbiomed.2013.05.050
    • (2013) Free Radical Biol. Med. , vol.65 , pp. 244-253
    • Turell, L.1    Radi, R.2    Alvarez, B.3
  • 30
    • 84906345897 scopus 로고    scopus 로고
    • Improving the serum stability of site-specific antibody conjugates with sulfone linkers
    • Patterson, J. T., Asano, S., Li, X., Rader, C., and Barbas, C. F., 3rd (2014) Improving the serum stability of site-specific antibody conjugates with sulfone linkers Bioconjugate Chem. 25, 1402-7 10.1021/bc500276m
    • (2014) Bioconjugate Chem. , vol.25 , pp. 1402-1407
    • Patterson, J.T.1    Asano, S.2    Li, X.3    Rader, C.4    Barbas, C.F.5
  • 31
    • 84887976957 scopus 로고    scopus 로고
    • Rapid, stable, chemoselective labeling of thiols with Julia-Kocienski-like reagents: A serum-stable alternative to maleimide-based protein conjugation
    • Toda, N., Asano, S., and Barbas, C. F., 3rd (2013) Rapid, stable, chemoselective labeling of thiols with Julia-Kocienski-like reagents: a serum-stable alternative to maleimide-based protein conjugation Angew. Chem., Int. Ed. 52, 12592-6 10.1002/anie.201306241
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 12592-12596
    • Toda, N.1    Asano, S.2    Barbas, C.F.3
  • 32
    • 84945561397 scopus 로고    scopus 로고
    • Organometallic palladium reagents for cysteine bioconjugation
    • Vinogradova, E. V., Zhang, C., Spokoyny, A. M., Pentelute, B. L., and Buchwald, S. L. (2015) Organometallic palladium reagents for cysteine bioconjugation Nature 526, 687-91 10.1038/nature15739
    • (2015) Nature , vol.526 , pp. 687-691
    • Vinogradova, E.V.1    Zhang, C.2    Spokoyny, A.M.3    Pentelute, B.L.4    Buchwald, S.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.