Chemical synthesis of proteins

被引:243
作者
Nilsson, BL
Soellner, MB
Raines, RT
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
来源
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE | 2005年 / 34卷
关键词
peptide synthesis; protein chemistry; proteomics; structural genomics;
D O I
10.1146/annurev.biophys.34.040204.144700
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins have become accessible targets for chemical synthesis. The basic strategy is to use native chemical ligation, Staudinger ligation, or other orthogonal chemical reactions to couple synthetic peptides. The ligation reactions are compatible with a variety of solvents and proceed in solution or on a solid support. Chemical synthesis enables a level of control on protein composition that greatly exceeds that attainable with ribosome-mediated biosynthesis. Accordingly, the chemical synthesis of proteins is providing previously unattainable insight into the structure and function of proteins.
引用
收藏
页码:91 / 118
页数:28
相关论文
共 157 条
[1]  
Aimoto S, 1999, BIOPOLYMERS, V51, P247, DOI 10.1002/(SICI)1097-0282(1999)51:4<247::AID-BIP2>3.0.CO
[2]  
2-W
[3]  
Albericio F, 1997, METHOD ENZYMOL, V289, P104
[4]   Developments in peptide and amide synthesis [J].
Albericio, F .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2004, 8 (03) :211-221
[5]  
Albericio F, 1997, METHOD ENZYMOL, V289, P313
[6]   High-level expression in Escherichia coli of selenocysteine-containing rat thioredoxin reductase utilizing gene fusions with engineered bacterial-type SECIS elements and co-expression with the selA, selB and selC genes [J].
Arnér, ESJ ;
Sarioglu, H ;
Lottspeich, F ;
Holmgren, A ;
Böck, A .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (05) :1003-1016
[7]   Protein prosthesis:: A nonnatural residue accelerates folding and increases stability [J].
Arnold, U ;
Hinderaker, MP ;
Köditz, J ;
Golbik, R ;
Ulbrich-Hofmann, R ;
Raines, RT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (25) :7500-7501
[8]   Protein prosthesis:: A semisynthetic enzyme with a β-peptide reverse turn [J].
Arnold, U ;
Hinderaker, MP ;
Nilsson, BL ;
Huck, BR ;
Gellman, SH ;
Raines, RT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (29) :8522-8523
[9]   Engineering the prion protein using chemical synthesis [J].
Ball, HL ;
King, DS ;
Cohen, FE ;
Prusiner, SB ;
Baldwin, MA .
JOURNAL OF PEPTIDE RESEARCH, 2001, 58 (05) :357-374
[10]   A one-pot total synthesis of crambin [J].
Bang, D ;
Kent, SBH .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (19) :2534-2538