Total chemical synthesis of proteins

被引:766
作者
Kent, Stephen B. H. [1 ]
机构
[1] Univ Chicago, Ctr Integrat Sci, Inst Biophys Dynam, Dept Chem, Chicago, IL 60637 USA
关键词
X-RAY-STRUCTURE; HIV-1; PROTEASE; CRYSTAL-STRUCTURE; LIGATION; PEPTIDE; ENZYME; ENANTIOMERS; RESIDUES;
D O I
10.1039/b700141j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This tutorial review outlines the modern ligation methods that enable the efficient total chemical synthesis of enzymes and other protein molecules. Key to this success is the chemoselective reaction of unprotected synthetic peptides ('chemical ligation'). Notably, native chemical ligation enables the reaction of two unprotected peptides in aqueous solution at neutral pH to form a single product in near quantitative yield. Full-length synthetic polypeptides are folded to form the defined tertiary structure of the target protein molecule, which is characterized by mass spectrometry, NMR, and X-ray crystallography, in addition to biochemical and/or biological activity.
引用
收藏
页码:338 / 351
页数:14
相关论文
共 43 条
[1]   CATALYTIC CONTRIBUTION OF FLAP-SUBSTRATE HYDROGEN-BONDS IN HIV-1 PROTEASE EXPLORED BY CHEMICAL SYNTHESIS [J].
BACA, M ;
KENT, SBH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11638-11642
[2]   Dissecting the energetics of protein α-helix C-cap termination through chemical protein synthesis [J].
Bang, D ;
Gribenko, AV ;
Tereshko, V ;
Kossiakoff, AA ;
Kent, SB ;
Makhatadze, GI .
NATURE CHEMICAL BIOLOGY, 2006, 2 (03) :139-143
[3]   Total chemical synthesis and X-ray crystal structure of a protein diastereomer: [D-Gln 35]ubiquitin [J].
Bang, D ;
Makhatadze, GI ;
Tereshko, V ;
Kossiakoff, AA ;
Kent, SB .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (25) :3852-3856
[4]   A one-pot total synthesis of crambin [J].
Bang, D ;
Kent, SBH .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (19) :2534-2538
[5]   Kinetically controlled ligation for the convergent chemical synthesis of proteins [J].
Bang, Duhee ;
Pentelute, Brad L. ;
Kent, Stephen B. H. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (24) :3985-3988
[6]   An efficient Fmoc-SPPS approach for the generation of thioester peptide precursors for use in native chemical ligation [J].
Blanco-Canosa, Juan B. ;
Dawson, Philip E. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (36) :6851-6855
[7]   Chemoselective amide ligations by decarboxylative condensations of N-alkylhydroxylamines and α-ketoacids [J].
Bode, JW ;
Fox, RM ;
Baucom, KD .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (08) :1248-1252
[8]   Peptide and protein building blocks for synthetic biology: From programming biomolecules to self-organized biomolecular systems [J].
Bromley, Elizabeth H. C. ;
Channon, Kevin ;
Moutevelis, Efrosini ;
Woolfson, Derek N. .
ACS CHEMICAL BIOLOGY, 2008, 3 (01) :38-50
[9]   TOTAL CHEMICAL SYNTHESIS OF A UNIQUE TRANSCRIPTION FACTOR-RELATED PROTEIN - CMYC-MAX [J].
CANNE, LE ;
FERREDAMARE, AR ;
BURLEY, SK ;
KENT, SBH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (11) :2998-3007
[10]   WEIGHING NAKED PROTEINS - PRACTICAL, HIGH-ACCURACY MASS MEASUREMENT OF PEPTIDES AND PROTEINS [J].
CHAIT, BT ;
KENT, SBH .
SCIENCE, 1992, 257 (5078) :1885-1894