Computational protein design promises to revolutionize protein engineering

被引:28
作者
Alvizo, Oscar [1 ]
Allen, Benjamin D.
Mayo, Stephen L.
机构
[1] CALTECH, Biochem & Mol Biophys Opt, Pasadena, CA 91125 USA
[2] CALTECH, Div Chem & Chem Engn, Pasadena, CA USA
[3] Howard Hughes Med Inst, Div Biol, Pasadena, CA 91125 USA
[4] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
D O I
10.2144/000112336
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Natural evolution has produced an astounding array of proteins that perform the physical and chemical functions required for life on Earth. Although proteins can be reengineered to provide altered or novel functions, the utility of this approach is limited by the difficulty of identifying protein sequences that display the desired properties. Recently, advances in the field of computational protein design (CPD) have shown that molecular simulation can help to predict sequences with new and improved functions. In the past few years, CPD has been used to design protein variants with optimized specificity of binding to DNA, small molecules, peptides, and other proteins. Initial successes in enzyme design highlight CPD's unique ability to design function de novo. The use of CPD for the engineering of potential therapeutic agents has demonstrated its strength in real-life applications.
引用
收藏
页码:31 / +
页数:5
相关论文
共 40 条
[1]   Dramatic performance enhancements for the FASTER optimization algorithm [J].
Allen, Benjamin D. ;
Mayo, Stephen L. .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2006, 27 (10) :1071-1075
[2]   Computational design of receptors for an organophosphate surrogate of the nerve agent soman [J].
Allert, M ;
Rizk, SS ;
Looger, LL ;
Hellinga, HW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (21) :7907-7912
[3]   Computational redesign of endonuclease DNA binding and cleavage specificity [J].
Ashworth, Justin ;
Havranek, James J. ;
Duarte, Carlos M. ;
Sussman, Django ;
Monnat, Raymond J., Jr. ;
Stoddard, Barry L. ;
Baker, David .
NATURE, 2006, 441 (7093) :656-659
[4]   Enzyme-like proteins by computational design [J].
Bolon, DN ;
Mayo, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14274-14279
[5]   EXCLUDED VOLUME APPROXIMATION TO PROTEIN-SOLVENT INTERACTION - THE SOLVENT CONTACT MODEL [J].
COLONNACESARI, F ;
SANDER, C .
BIOPHYSICAL JOURNAL, 1990, 57 (05) :1103-1107
[6]   Probing the role of packing specificity in protein design [J].
Dahiyat, BI ;
Mayo, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10172-10177
[7]   Automated design of the surface positions of protein helices [J].
Dahiyat, BI ;
Gordon, DB ;
Mayo, SL .
PROTEIN SCIENCE, 1997, 6 (06) :1333-1337
[8]   DE-NOVO DESIGN OF THE HYDROPHOBIC CORES OF PROTEINS [J].
DESJARLAIS, JR ;
HANDEL, TM .
PROTEIN SCIENCE, 1995, 4 (10) :2006-2018
[9]   THE DEAD-END ELIMINATION THEOREM AND ITS USE IN PROTEIN SIDE-CHAIN POSITIONING [J].
DESMET, J ;
DEMAEYER, M ;
HAZES, B ;
LASTERS, I .
NATURE, 1992, 356 (6369) :539-542
[10]   Fast and Accurate Side-Chain Topology and Energy Refinement (FASTER) as a new method for protein structure optimization [J].
Desmet, J ;
Spriet, J ;
Lasters, I .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 2002, 48 (01) :31-43