Enzyme redesign

被引:106
作者
Penning, TM
Jez, JM
机构
[1] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[2] Salk Inst Biol Studies, Struct Biol Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1021/cr000049n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The various techniques used for enzyme redesigning were discussed. The process enzyme redesign addresses questions of catalysis and ligand recognition and provides a basis for the applied use of engineered enzymes. The results show that modification of stereochemical outcome of a reaction has practical benefits as many enzymes serve as chiral catalysts for synthetic purposes in the chemical and pharmaceutical industry.
引用
收藏
页码:3027 / 3046
页数:20
相关论文
共 165 条
[31]   Unnatural amino acids as probes of protein structure and function [J].
Dougherty, DA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (06) :645-652
[32]   Synthesis of amidrazones using an engineered papain nitrile hydratase [J].
Dufour, E ;
Tam, W ;
Nägler, DK ;
Storer, AC ;
Ménard, R .
FEBS LETTERS, 1998, 433 (1-2) :78-82
[33]   Engineering nitrile hydratase activity into a cysteine protease by a single mutation [J].
Dufour, E ;
Storer, AC ;
Menard, R .
BIOCHEMISTRY, 1995, 34 (50) :16382-16388
[34]   Redesigning the substrate specificity of human O6-alkylguanine-DNA alkyltransferase.: Mutants with enhanced repair of O4-methylthymine [J].
Encell, LP ;
Loeb, LA .
BIOCHEMISTRY, 1999, 38 (37) :12097-12103
[35]   SITE-DIRECTED MUTAGENESIS OF BETA-LACTAMASE LEADING TO ACCUMULATION OF A CATALYTIC INTERMEDIATE [J].
ESCOBAR, WA ;
TAN, AK ;
FINK, AL .
BIOCHEMISTRY, 1991, 30 (44) :10783-10787
[36]   Modified substrate specificity of L-hydroxyisocaproate dehydrogenase derived from structure-based protein engineering [J].
Feil, IK ;
Hendle, J ;
Schomburg, D .
PROTEIN ENGINEERING, 1997, 10 (03) :255-262
[37]   HYDROGEN-BONDING AND BIOLOGICAL SPECIFICITY ANALYZED BY PROTEIN ENGINEERING [J].
FERSHT, AR ;
SHI, JP ;
KNILLJONES, J ;
LOWE, DM ;
WILKINSON, AJ ;
BLOW, DM ;
BRICK, P ;
CARTER, P ;
WAYE, MMY ;
WINTER, G .
NATURE, 1985, 314 (6008) :235-238
[38]   SMALL-MOLECULE BINDING TO AN ARTIFICIALLY CREATED CAVITY AT THE ACTIVE-SITE OF CYTOCHROME-C PEROXIDASE [J].
FITZGERALD, MM ;
CHURCHILL, MJ ;
MCREE, DE ;
GOODIN, DB .
BIOCHEMISTRY, 1994, 33 (13) :3807-3818
[39]   Directed evolution of D-2-keto-3-deoxy-6-phosphogluconate aldolase to new variants for the efficient synthesis of D- and L-sugars [J].
Fong, S ;
Machajewski, TD ;
Mak, CC ;
Wong, CH .
CHEMISTRY & BIOLOGY, 2000, 7 (11) :873-883
[40]   Conversion of aspartate aminotransferase into an L-aspartate β-decarboxylase by a triple active-site mutation [J].
Graber, R ;
Kasper, P ;
Malashkevich, VN ;
Strop, P ;
Gehring, H ;
Jansonius, JN ;
Christen, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (44) :31203-31208