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Volumn 14, Issue 2, 2008, Pages 224-240

RAFT Nano-constructs: Surfing to biological applications

Author keywords

Cyclopeptide; Molecular recognition; Oxime; Protein mimic; Sensor; Synthetic vaccine; Targeting; Template

Indexed keywords

AMYLOID BETA PROTEIN; ANTINEOPLASTIC AGENT; ARGINYLGLYCYLASPARTIC ACID; CANCER VACCINE; CARBOHYDRATE; CHAPERONE; GALACTOSE OXIDASE; NANOMATERIAL; NANOTUBE; NUCLEIC ACID; PEPTIDE; PEPTIDE DERIVATIVE; ZINC FINGER PROTEIN;

EID: 39649094295     PISSN: 10752617     EISSN: 10991387     Source Type: Journal    
DOI: 10.1002/psc.964     Document Type: Review
Times cited : (59)

References (72)
  • 2
    • 0024039077 scopus 로고
    • Nature's rules and chemist's tools: A way for creating novel proteins
    • Mutter M. Nature's rules and chemist's tools: a way for creating novel proteins. Trends Biochem. Sci. 1988; 13: 260-265.
    • (1988) Trends Biochem. Sci , vol.13 , pp. 260-265
    • Mutter, M.1
  • 3
    • 0009673779 scopus 로고
    • Marshall G. R ed, ESCOM: Leiden, The Netherlands
    • Mutter M. In Peptides: Chemistry and Biology. Marshall G. R (ed.). ESCOM: Leiden, The Netherlands, 1988; 349-354.
    • (1988) Peptides: Chemistry and Biology , pp. 349-354
    • Mutter, M.1
  • 4
    • 0032538776 scopus 로고    scopus 로고
    • New protein mimetics: The zinc finger motif as a locked-in tertiary fold
    • Tuchscherer G, Lehmann C, Mathieu M. New protein mimetics: the zinc finger motif as a locked-in tertiary fold. Angew. Chem., Int. Ed. 1998; 37: 2990-2993.
    • (1998) Angew. Chem., Int. Ed , vol.37 , pp. 2990-2993
    • Tuchscherer, G.1    Lehmann, C.2    Mathieu, M.3
  • 5
    • 4544282330 scopus 로고    scopus 로고
    • New protein mimetics: The zinc finger motif as a locked-in tertiary fold
    • Tuchscherer G, Lehmann C, Mathieu M. New protein mimetics: the zinc finger motif as a locked-in tertiary fold. Angew. Chem. 1998; 110: 3160-3164.
    • (1998) Angew. Chem , vol.110 , pp. 3160-3164
    • Tuchscherer, G.1    Lehmann, C.2    Mathieu, M.3
  • 6
    • 0027092804 scopus 로고
    • Total chemical synthesis, characterization, and immunological properties of an MHC class I model using the TASP concept for protein de novo design
    • Tuchscherer G, Servis C, Corradin G, Blum U, Rivier J, Mutter M. Total chemical synthesis, characterization, and immunological properties of an MHC class I model using the TASP concept for protein de novo design. Protein Sci. 1992; 1: 1377-1386.
    • (1992) Protein Sci , vol.1 , pp. 1377-1386
    • Tuchscherer, G.1    Servis, C.2    Corradin, G.3    Blum, U.4    Rivier, J.5    Mutter, M.6
  • 8
    • 0024574972 scopus 로고
    • Helichrome: Synthesis and enzymic activity of a designed hemeprotein
    • Sasaki T, Kaiser ET. Helichrome: synthesis and enzymic activity of a designed hemeprotein. J. Am. Chem. Soc. 1989; 111: 380-381.
    • (1989) J. Am. Chem. Soc , vol.111 , pp. 380-381
    • Sasaki, T.1    Kaiser, E.T.2
  • 9
    • 0036968892 scopus 로고    scopus 로고
    • Design and synthesis of multiple-loop receptors based on a calix[4]arene scaffold for protein surface recognition
    • Lin Q, Hamilton AD. Design and synthesis of multiple-loop receptors based on a calix[4]arene scaffold for protein surface recognition. C. R. Chimie 2002; 5: 441-450.
    • (2002) C. R. Chimie , vol.5 , pp. 441-450
    • Lin, Q.1    Hamilton, A.D.2
  • 10
    • 33144477183 scopus 로고    scopus 로고
    • Carbohydrates in peptide and protein design
    • Jensen KJ, Brask J. Carbohydrates in peptide and protein design. Biopolymers 2005; 80: 747-761.
    • (2005) Biopolymers , vol.80 , pp. 747-761
    • Jensen, K.J.1    Brask, J.2
  • 11
    • 0028878086 scopus 로고
    • A convenient synthesis of cyclic peptides as regioselectively addressable functionalized templates (RAFT)
    • Dumy P, Eggleston IM, Cervigni S, Sila U, Sun X, Mutter M. A convenient synthesis of cyclic peptides as regioselectively addressable functionalized templates (RAFT). Tetrahedron Lett. 1995; 36: 1255-1258.
    • (1995) Tetrahedron Lett , vol.36 , pp. 1255-1258
    • Dumy, P.1    Eggleston, I.M.2    Cervigni, S.3    Sila, U.4    Sun, X.5    Mutter, M.6
  • 12
    • 0030249565 scopus 로고    scopus 로고
    • Solution structure of regioselectively addressable functionalized templates: An NMR and restrained molecular dynamics investigation
    • Dumy P, Eggleston IM, Esposito G, Nicula S, Mutter M. Solution structure of regioselectively addressable functionalized templates: an NMR and restrained molecular dynamics investigation. Biopolymers 1996; 39: 297-308.
    • (1996) Biopolymers , vol.39 , pp. 297-308
    • Dumy, P.1    Eggleston, I.M.2    Esposito, G.3    Nicula, S.4    Mutter, M.5
  • 13
    • 0000021544 scopus 로고
    • A chemical method for new proteins. Template-associated synthetic proteins (TASP)
    • Mutter M. Vuilleumier S. A chemical method for new proteins. Template-associated synthetic proteins (TASP). Angew. Chem. 1989; 101: 551-692.
    • (1989) Angew. Chem , vol.101 , pp. 551-692
    • Mutter, M.1    Vuilleumier, S.2
  • 14
    • 0024665396 scopus 로고
    • A chemical method for new proteins. Template-associated synthetic proteins (TASP)
    • Mutter M, Vuilleumier S. A chemical method for new proteins. Template-associated synthetic proteins (TASP). Angew. Chem., Int. Ed. 1989; 28: 1535-1554.
    • (1989) Angew. Chem., Int. Ed , vol.28 , pp. 1535-1554
    • Mutter, M.1    Vuilleumier, S.2
  • 15
    • 0027195926 scopus 로고
    • The template-assembled synthetic protein (TASP) concept: Mimetics of peptide ligands, protein surfaces and folding units
    • Tuchscherer G, Doemer B, Sila U, Kamber B, Mutter M. The template-assembled synthetic protein (TASP) concept: mimetics of peptide ligands, protein surfaces and folding units. Tetrahedron 1993; 49: 3559-3575.
    • (1993) Tetrahedron , vol.49 , pp. 3559-3575
    • Tuchscherer, G.1    Doemer, B.2    Sila, U.3    Kamber, B.4    Mutter, M.5
  • 16
    • 0029952823 scopus 로고    scopus 로고
    • Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis
    • Woehr T. Wahl F, Nefzi A, Rohwedder B, Sato T, Sun X, Mutter M. Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis. J. Am. Chem. Soc. 1996; 118: 9218-9227.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 9218-9227
    • Woehr, T.1    Wahl, F.2    Nefzi, A.3    Rohwedder, B.4    Sato, T.5    Sun, X.6    Mutter, M.7
  • 17
    • 0027756777 scopus 로고
    • Template assembled synthetic proteins: Condensation of a multifunctional peptide to a topological template via chemoselective ligation
    • Tuchscherer G. Template assembled synthetic proteins: condensation of a multifunctional peptide to a topological template via chemoselective ligation. Tetrahedron Lett. 1993; 34: 8419-8422.
    • (1993) Tetrahedron Lett , vol.34 , pp. 8419-8422
    • Tuchscherer, G.1
  • 18
    • 0000439676 scopus 로고
    • Convenient total synthesis of a 4-helix template-assembled synthetic protein (TASP) molecule by chemoselective ligation
    • Dawson PE, Kent SBH. Convenient total synthesis of a 4-helix template-assembled synthetic protein (TASP) molecule by chemoselective ligation. J. Am. Chem. Soc. 1993; 115: 7263-7266.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 7263-7266
    • Dawson, P.E.1    Kent, S.B.H.2
  • 19
    • 12044253737 scopus 로고
    • Chemical ligation approach to form a peptide bond between unprotected peptide segments. Concept and model study
    • Liu CF, Tam JP. Chemical ligation approach to form a peptide bond between unprotected peptide segments. Concept and model study. J. Am. Chem. Soc. 1994; 116: 4149-4153.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 4149-4153
    • Liu, C.F.1    Tam, J.P.2
  • 20
    • 0028231302 scopus 로고
    • Facile synthesis of homogeneous artificial proteins
    • Rose K. Facile synthesis of homogeneous artificial proteins. J. Am. Chem. Soc. 1994; 116: 30-33.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 30-33
    • Rose, K.1
  • 21
    • 0032863980 scopus 로고    scopus 로고
    • Extending the concept of template-assembled synthetic proteins
    • Tuchscherer G, Grell D, Mathieu M, Mutter M. Extending the concept of template-assembled synthetic proteins. J. Pept. Res. 1999; 54: 185-194.
    • (1999) J. Pept. Res , vol.54 , pp. 185-194
    • Tuchscherer, G.1    Grell, D.2    Mathieu, M.3    Mutter, M.4
  • 22
    • 0031434205 scopus 로고    scopus 로고
    • Non-native architectures in protein design and mimicry
    • Mutter M, Tuchscherer G. Non-native architectures in protein design and mimicry. Cell. Mol. Life Sci. 1997; 53: 851-863.
    • (1997) Cell. Mol. Life Sci , vol.53 , pp. 851-863
    • Mutter, M.1    Tuchscherer, G.2
  • 23
    • 0029113920 scopus 로고
    • Templates in protein de novo design
    • Tuchscherer G, Mutter M. Templates in protein de novo design. J. Biotechnol. 1995; 41: 197-210.
    • (1995) J. Biotechnol , vol.41 , pp. 197-210
    • Tuchscherer, G.1    Mutter, M.2
  • 24
    • 0035109565 scopus 로고    scopus 로고
    • Conformation and ion channel properties of a five-helix bundle protein
    • De E, Chaloin L, Heitz A, Mery J, Molle G, Heitz F. Conformation and ion channel properties of a five-helix bundle protein. J. Pept. Sci. 2001; 7: 41-49.
    • (2001) J. Pept. Sci , vol.7 , pp. 41-49
    • De, E.1    Chaloin, L.2    Heitz, A.3    Mery, J.4    Molle, G.5    Heitz, F.6
  • 25
    • 0028831838 scopus 로고
    • Chemoselective ligation of multifunctional peptides to topological templates via thioether formation for TASP synthesis
    • Nefzi A, Sun X, Mutter M. Chemoselective ligation of multifunctional peptides to topological templates via thioether formation for TASP synthesis. Tetrahedron Lett. 1995; 36: 229-230.
    • (1995) Tetrahedron Lett , vol.36 , pp. 229-230
    • Nefzi, A.1    Sun, X.2    Mutter, M.3
  • 26
    • 0034059760 scopus 로고    scopus 로고
    • Novel strategy for the synthesis of template-assembled analogues of rat relaxin
    • Mathieu MN, Wade JD, Tan Y-Y, Summers RJ, Tregear GW. Novel strategy for the synthesis of template-assembled analogues of rat relaxin. J. Pept. Sci. 2000; 6: 235-242.
    • (2000) J. Pept. Sci , vol.6 , pp. 235-242
    • Mathieu, M.N.1    Wade, J.D.2    Tan, Y.-Y.3    Summers, R.J.4    Tregear, G.W.5
  • 27
    • 9344222203 scopus 로고    scopus 로고
    • Versatile synthesis of boc protected hydrazinoacetic acid and its application to the chemoselective ligation of tasp molecules
    • Banfi D, Mutter M, Patiny L. Versatile synthesis of boc protected hydrazinoacetic acid and its application to the chemoselective ligation of tasp molecules. Prolein Pept. Lett. 2004; 11: 539-542.
    • (2004) Prolein Pept. Lett , vol.11 , pp. 539-542
    • Banfi, D.1    Mutter, M.2    Patiny, L.3
  • 28
    • 0035903508 scopus 로고    scopus 로고
    • Highly efficient synthesis of peptide-oligonucleotide conjugates: Chemoselective oxime and thiazolidine formation
    • Forget D, Boturyn D, Defrancq E, Lhomme J, Dumy P. Highly efficient synthesis of peptide-oligonucleotide conjugates: chemoselective oxime and thiazolidine formation. Chem. - Eur. J. 2001; 7: 3976-3984.
    • (2001) Chem. - Eur. J , vol.7 , pp. 3976-3984
    • Forget, D.1    Boturyn, D.2    Defrancq, E.3    Lhomme, J.4    Dumy, P.5
  • 29
    • 9644266960 scopus 로고    scopus 로고
    • New strategy for the synthesis of 3′, 5′ bifunctionalised oligonucleotide conjugates through sequential formation of chemoselective oxime bonds
    • Edupuganti OP, Singh Y, Defrancq E, Dumy P. New strategy for the synthesis of 3′, 5′ bifunctionalised oligonucleotide conjugates through sequential formation of chemoselective oxime bonds. Chem. Eur. J. 2004; 10: 5988-5995.
    • (2004) Chem. Eur. J , vol.10 , pp. 5988-5995
    • Edupuganti, O.P.1    Singh, Y.2    Defrancq, E.3    Dumy, P.4
  • 30
    • 0034714255 scopus 로고    scopus 로고
    • Synthesis of methylketone containing nucleoside triphosphates for RNA labelling
    • Trévisiol E, Defrancq E, Lhomme J, Laayoun A, Cros P. Synthesis of methylketone containing nucleoside triphosphates for RNA labelling. Tetrahedron 2000; 56: 6501-6510.
    • (2000) Tetrahedron , vol.56 , pp. 6501-6510
    • Trévisiol, E.1    Defrancq, E.2    Lhomme, J.3    Laayoun, A.4    Cros, P.5
  • 31
    • 34347350294 scopus 로고    scopus 로고
    • Efficient surface patterning of oligonucleotides inside a glass capillary through oxime bond formation
    • Dendane N, Hoang A, Guillard L, Defrancq E, Vinet F, Dumy P. Efficient surface patterning of oligonucleotides inside a glass capillary through oxime bond formation. BioConjugate Chem. 2007; 18: 671-676.
    • (2007) BioConjugate Chem , vol.18 , pp. 671-676
    • Dendane, N.1    Hoang, A.2    Guillard, L.3    Defrancq, E.4    Vinet, F.5    Dumy, P.6
  • 32
    • 0035832069 scopus 로고    scopus 로고
    • 5 integrin ligand conjugates: Regioselective solid-phase functionalisation of an RGD based peptide
    • 5 integrin ligand conjugates: regioselective solid-phase functionalisation of an RGD based peptide. Teirahedron Lett. 2001; 42: 2787-2790.
    • (2001) Teirahedron Lett , vol.42 , pp. 2787-2790
    • Boturyn, D.1    Dumy, P.2
  • 33
    • 33645022683 scopus 로고    scopus 로고
    • Chemoselectively addressable template: A valuable tool for the engineering of molecular conjugates
    • Garanger E, Boturyn D, Renaudet O, Defrancq E, Dumy P. Chemoselectively addressable template: a valuable tool for the engineering of molecular conjugates. J. Org. Chem. 2006; 71: 2402-2410.
    • (2006) J. Org. Chem , vol.71 , pp. 2402-2410
    • Garanger, E.1    Boturyn, D.2    Renaudet, O.3    Defrancq, E.4    Dumy, P.5
  • 34
    • 21744438268 scopus 로고    scopus 로고
    • Synthesis of multitopic neoglycopeptides displaying recognition and detection motifs
    • Renaudet O, Dumy P. Synthesis of multitopic neoglycopeptides displaying recognition and detection motifs. Bioorg. Med. Chem. Lett. 2005; 15: 3619-3622.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 3619-3622
    • Renaudet, O.1    Dumy, P.2
  • 35
    • 0035935115 scopus 로고    scopus 로고
    • Expedient synthesis of aminooxylated-carbohydrates for chemoselective access of glycoconjugates
    • Renaudet O, Dumy P. Expedient synthesis of aminooxylated-carbohydrates for chemoselective access of glycoconjugates. Tetrahedron Lett. 2001; 42: 7575-7578.
    • (2001) Tetrahedron Lett , vol.42 , pp. 7575-7578
    • Renaudet, O.1    Dumy, P.2
  • 36
    • 17444422910 scopus 로고    scopus 로고
    • Preparation of a multitopic glycopeptide oligonucleotide conjugate
    • Singh Y, Renaudet O, Defrancq E, Dumy P. Preparation of a multitopic glycopeptide oligonucleotide conjugate. Org. Lett. 2005; 7: 1359-1362.
    • (2005) Org. Lett , vol.7 , pp. 1359-1362
    • Singh, Y.1    Renaudet, O.2    Defrancq, E.3    Dumy, P.4
  • 39
    • 2442620150 scopus 로고    scopus 로고
    • Template assembled eyelopeptides as multimerie system for integrin targeting and endocytosis
    • Boturyn D, Coll JL, Garanger E, Favrot MC, Dumy P. Template assembled eyelopeptides as multimerie system for integrin targeting and endocytosis. J. Am. Chem. Soc. 2004; 126: 5730-5739.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 5730-5739
    • Boturyn, D.1    Coll, J.L.2    Garanger, E.3    Favrot, M.C.4    Dumy, P.5
  • 41
    • 28444471558 scopus 로고    scopus 로고
    • New multifunctional molecular conjugate vector for targeting, imaging and therapy of tumors
    • Garanger E, Boturyn D, Jin Z, Dumy P, Favrot MC, Coll JL. New multifunctional molecular conjugate vector for targeting, imaging and therapy of tumors. Mol. Ther. 2005; 12: 1168-1175.
    • (2005) Mol. Ther , vol.12 , pp. 1168-1175
    • Garanger, E.1    Boturyn, D.2    Jin, Z.3    Dumy, P.4    Favrot, M.C.5    Coll, J.L.6
  • 45
    • 0032951071 scopus 로고    scopus 로고
    • In vivo imaging of tumors with protease-activated near-infrared fluorescent probes
    • Weissleder R, Tung CH, Mahmood U, Bogdanov A Jr. In vivo imaging of tumors with protease-activated near-infrared fluorescent probes. Nat. Biotechnol. 1999; 17: 375-378.
    • (1999) Nat. Biotechnol , vol.17 , pp. 375-378
    • Weissleder, R.1    Tung, C.H.2    Mahmood, U.3    Bogdanov Jr., A.4
  • 46
    • 0034283034 scopus 로고    scopus 로고
    • In vivo imaging of proteolytic enzyme activity using a novel molecular reporter
    • Tung CH, Mahmood U, Bredow S, Weissleder R. In vivo imaging of proteolytic enzyme activity using a novel molecular reporter. Cancer Res. 2000; 60: 4953-4958.
    • (2000) Cancer Res , vol.60 , pp. 4953-4958
    • Tung, C.H.1    Mahmood, U.2    Bredow, S.3    Weissleder, R.4
  • 47
    • 0034954524 scopus 로고    scopus 로고
    • In vivo molecular target assessment of matrix metalloproteinase inhibition
    • Bremer C, Tung CH, Weissleder R. In vivo molecular target assessment of matrix metalloproteinase inhibition. Nat. Med. 2001; 7: 743-748.
    • (2001) Nat. Med , vol.7 , pp. 743-748
    • Bremer, C.1    Tung, C.H.2    Weissleder, R.3
  • 49
    • 0742304469 scopus 로고    scopus 로고
    • Synthesis of multivalent chemoselectively template-assembled glycopeptide presenting the cancer related T-antigen
    • Renaudet O, Dumy P. Synthesis of multivalent chemoselectively template-assembled glycopeptide presenting the cancer related T-antigen. Tetrahedron Lett. 2004; 45: 65-68.
    • (2004) Tetrahedron Lett , vol.45 , pp. 65-68
    • Renaudet, O.1    Dumy, P.2
  • 50
    • 25444439256 scopus 로고    scopus 로고
    • Chemoselective assembly and immunological evaluation of multiepitopic glycoconjugates bearing clustered Tn antigen as synthetic anticancer vaccine
    • Grigalevicius S, Chierici S, Renaudet O, Lo-Man R, Dériaud E, Leclerc C, Dumy P. Chemoselective assembly and immunological evaluation of multiepitopic glycoconjugates bearing clustered Tn antigen as synthetic anticancer vaccine. Bioconjugate Chem. 2005; 5: 1149-1159.
    • (2005) Bioconjugate Chem , vol.5 , pp. 1149-1159
    • Grigalevicius, S.1    Chierici, S.2    Renaudet, O.3    Lo-Man, R.4    Dériaud, E.5    Leclerc, C.6    Dumy, P.7
  • 51
    • 0030848719 scopus 로고    scopus 로고
    • Immunoreactive T and Tn epitopes in cancer diagnosis, prognosis, and immunotherapy
    • Springer GF. Immunoreactive T and Tn epitopes in cancer diagnosis, prognosis, and immunotherapy. J. Mol. Med. 1997; 75: 594-602.
    • (1997) J. Mol. Med , vol.75 , pp. 594-602
    • Springer, G.F.1
  • 52
    • 0033118481 scopus 로고    scopus 로고
    • A fully synthetic immunogen carrying a carcinoma-associated carbohydrate for active specific immunotherapy
    • Lo-Man R, Bay S, Vichier Guerre S, Dériaud E, Cantacuzéne D, Leclerc C. A fully synthetic immunogen carrying a carcinoma-associated carbohydrate for active specific immunotherapy. Cancer Res. 1999; 59: 1520-1524.
    • (1999) Cancer Res , vol.59 , pp. 1520-1524
    • Lo-Man, R.1    Bay, S.2    Vichier Guerre, S.3    Dériaud, E.4    Cantacuzéne, D.5    Leclerc, C.6
  • 53
    • 34250750826 scopus 로고    scopus 로고
    • Novel template-assembled oligosaccharide clusters as epitope mimics for HIV-neutralizing antibody 2G12. Design, synthesis, and antibody binding study
    • Wang J, Li H, Zou G, Wang LX. Novel template-assembled oligosaccharide clusters as epitope mimics for HIV-neutralizing antibody 2G12. Design, synthesis, and antibody binding study. Org. Bioorg. Chem. 2007; 5: 1529-1540.
    • (2007) Org. Bioorg. Chem , vol.5 , pp. 1529-1540
    • Wang, J.1    Li, H.2    Zou, G.3    Wang, L.X.4
  • 55
    • 0032573867 scopus 로고    scopus 로고
    • Design, synthesis, and properties of a novel cytochrome b Model
    • Rau HK, Haehnel W. Design, synthesis, and properties of a novel cytochrome b Model. J. Am. Chem. Soc. 1998; 120: 468-476.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 468-476
    • Rau, H.K.1    Haehnel, W.2
  • 56
    • 0034801581 scopus 로고    scopus 로고
    • De novo design and characterization of copper centres in synthetic four helix-bundle proteins
    • Schnepf R, Hoerth P, Bill E, Wieghardt K, Hildebrandt P, Haehnel W. De novo design and characterization of copper centres in synthetic four helix-bundle proteins. J. Am. Chem. Soc. 2001; 123: 2186-2195.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 2186-2195
    • Schnepf, R.1    Hoerth, P.2    Bill, E.3    Wieghardt, K.4    Hildebrandt, P.5    Haehnel, W.6
  • 57
    • 7744232977 scopus 로고    scopus 로고
    • Spectroscopic identification of different types of copper centres generated in synthetic four-helix bundle proteins
    • Schnepf R, Haehnel W, Wieghardt K, Hildebrandt P. Spectroscopic identification of different types of copper centres generated in synthetic four-helix bundle proteins. J. Am. Chem. Soc. 2004; 126: 14389-14399.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 14389-14399
    • Schnepf, R.1    Haehnel, W.2    Wieghardt, K.3    Hildebrandt, P.4
  • 58
    • 0012310464 scopus 로고    scopus 로고
    • Combinatorial synthesis of four-helix bundle hemoproteins for tuning of cofactor properties
    • Rau HK, DeJonge N, Haehnel W. Combinatorial synthesis of four-helix bundle hemoproteins for tuning of cofactor properties. Angew. Chem. 2000; 112: 2256-2259.
    • (2000) Angew. Chem , vol.112 , pp. 2256-2259
    • Rau, H.K.1    DeJonge, N.2    Haehnel, W.3
  • 59
    • 0034598552 scopus 로고    scopus 로고
    • Combinatorial synthesis of four-helix bundle hemoproteins for tuning of cofactor properties
    • Rau HK, DeJonge N, Haehnel W. Combinatorial synthesis of four-helix bundle hemoproteins for tuning of cofactor properties. Angew. Chem. Int. Ed. 2000; 39: 250-253.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 250-253
    • Rau, H.K.1    DeJonge, N.2    Haehnel, W.3
  • 60
    • 4043144341 scopus 로고    scopus 로고
    • Chemical synthesis of TASP arrays and their application in protein design
    • Haehnel W. Chemical synthesis of TASP arrays and their application in protein design. Mol. Divers. 2004; 8: 219-229.
    • (2004) Mol. Divers , vol.8 , pp. 219-229
    • Haehnel, W.1
  • 62
    • 33748531485 scopus 로고    scopus 로고
    • Control of amyloid β-peptide protofibril formation by a designed template assembly
    • Dolphin GT, Dumy P, Garcia J. Control of amyloid β-peptide protofibril formation by a designed template assembly. Angew. Chem. 2006; 118: 2765-2768.
    • (2006) Angew. Chem , vol.118 , pp. 2765-2768
    • Dolphin, G.T.1    Dumy, P.2    Garcia, J.3
  • 63
    • 33746216304 scopus 로고    scopus 로고
    • Control of amyloid β-peptide protofibril formation by a designed template assembly
    • Dolphin GT, Dumy P, Garcia J. Control of amyloid β-peptide protofibril formation by a designed template assembly. Angew. Chem. Int. Ed. 2006; 45: 2699-2702.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 2699-2702
    • Dolphin, G.T.1    Dumy, P.2    Garcia, J.3
  • 64
    • 0002444467 scopus 로고    scopus 로고
    • Engineering of zinc finger and MHC motifs to locked-in tertiary folds
    • Mathieu M, Lehmann C, Razaname A, Tuchscherer G. Engineering of zinc finger and MHC motifs to locked-in tertiary folds. Lett. Pept. Sci. 1997; 4: 95-100.
    • (1997) Lett. Pept. Sci , vol.4 , pp. 95-100
    • Mathieu, M.1    Lehmann, C.2    Razaname, A.3    Tuchscherer, G.4
  • 69
    • 25144483773 scopus 로고    scopus 로고
    • Electrochemical detection of arachis hypogaea (peanut) agglutinin binding to monovalent and clustered lactosyl motifs immobilized on a polypyrrole film
    • Dubois MP, Gondran C, Renaudet O, Dumy P, Driguez H, Fort S, Cosnier S. Electrochemical detection of arachis hypogaea (peanut) agglutinin binding to monovalent and clustered lactosyl motifs immobilized on a polypyrrole film. Chem. Commun. 2005; 34: 4318-4320.
    • (2005) Chem. Commun , vol.34 , pp. 4318-4320
    • Dubois, M.P.1    Gondran, C.2    Renaudet, O.3    Dumy, P.4    Driguez, H.5    Fort, S.6    Cosnier, S.7
  • 70
    • 0037504266 scopus 로고    scopus 로고
    • Chemoselectively template-assembled glycoconjugates as mimics for multivalent presentation of carbohydrates
    • Renaudet O, Dumy P. Chemoselectively template-assembled glycoconjugates as mimics for multivalent presentation of carbohydrates. Org. Lett. 2003, 5: 243.
    • (2003) Org. Lett , vol.5 , pp. 243
    • Renaudet, O.1    Dumy, P.2
  • 71
    • 33745469304 scopus 로고    scopus 로고
    • On-bead synthesis and binding assay of chemoselectively template-assembled multivalent neoglycopeptides
    • Renaudet O, Dumy P. On-bead synthesis and binding assay of chemoselectively template-assembled multivalent neoglycopeptides. Org. Biomol. Chem. 2006; 4: 2628-2636.
    • (2006) Org. Biomol. Chem , vol.4 , pp. 2628-2636
    • Renaudet, O.1    Dumy, P.2
  • 72
    • 33748865392 scopus 로고    scopus 로고
    • Redox-active biomolecular architectures and self-assembled monolayers based on a cyclodecapeptide regioselectively addressable functional template
    • Devilliers CH, Boturyn D, Bucher C, Dumy P, Labbé P, Moutet JC, Royal G, Saint Aman E. Redox-active biomolecular architectures and self-assembled monolayers based on a cyclodecapeptide regioselectively addressable functional template. Langmuir 2006; 22: 8134-8143.
    • (2006) Langmuir , vol.22 , pp. 8134-8143
    • Devilliers, C.H.1    Boturyn, D.2    Bucher, C.3    Dumy, P.4    Labbé, P.5    Moutet, J.C.6    Royal, G.7    Saint Aman, E.8


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