The process of structure-based drug design

被引:571
作者
Anderson, AC [1 ]
机构
[1] Dartmouth Coll, Dept Chem, Burke Labs, Hanover, NH 03755 USA
来源
CHEMISTRY & BIOLOGY | 2003年 / 10卷 / 09期
关键词
D O I
10.1016/j.chembiol.2003.09.002
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
The field of structure-based drug design is a rapidly growing area in which many successes have occurred in recent years. The explosion of genomic, proteomic, and structural information has provided hundreds of new targets and opportunities for future drug lead discovery. This review summarizes the process of structure-based drug design and includes, primarily, the choice of a target, the evaluation of a structure of that target, the pivotal questions to consider in choosing a method for drug lead discovery, and evaluation of the drug leads. Key principles in the field of structure-based drug design will be illustrated through a case study that explores drug design for AmpC beta-lactamase.
引用
收藏
页码:787 / 797
页数:11
相关论文
共 101 条
[11]  
BOHM HJ, 1992, J COMPUT AID MOL DES, V6, P61, DOI 10.1007/bf00124387
[12]   MULTIPLE COPY SIMULTANEOUS SEARCH AND CONSTRUCTION OF LIGANDS IN BINDING-SITES - APPLICATION TO INHIBITORS OF HIV-1 ASPARTIC PROTEINASE [J].
CAFLISCH, A ;
MIRANKER, A ;
KARPLUS, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (15) :2142-2167
[13]   Developing a dynamic pharmacophore model for HIV-1 integrase [J].
Carlson, HA ;
Masukawa, KM ;
Rubins, K ;
Bushman, FD ;
Jorgensen, WL ;
Lins, RD ;
Briggs, JM ;
McCammon, JA .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (11) :2100-2114
[14]   Protein flexibility and drug design: how to hit a moving target [J].
Carlson, HA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (04) :447-452
[15]  
Carlson HA, 2000, MOL PHARMACOL, V57, P213
[16]   Method for including the dynamic fluctuations of a protein in computer-aided drug design [J].
Carlson, HA ;
Masukawa, KM ;
McCammon, JA .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (49) :10213-10219
[17]   COMPARISON OF HOMOLOGY MODELS WITH THE EXPERIMENTAL STRUCTURE OF A NOVEL SERINE-PROTEASE [J].
CARSON, M ;
BUGG, CE ;
DELUCAS, LJ ;
NARAYANA, SVL .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 1994, 50 :889-899
[18]   Structural studies on bioactive compounds.: 34.: Design, synthesis, and biological evaluation of triazenyl-substituted pyrimethamine inhibitors of Pneumocystis carinii dihydrofolate reductase [J].
Chan, DCM ;
Laughton, CA ;
Queener, SF ;
Stevens, MFG .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (16) :2555-2564
[19]   FlexE: Efficient molecular docking considering protein structure variations [J].
Claussen, H ;
Buning, C ;
Rarey, M ;
Lengauer, T .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 308 (02) :377-395
[20]  
Davis AM, 1999, ANGEW CHEM INT EDIT, V38, P737, DOI 10.1002/(SICI)1521-3773(19990315)38:6<736::AID-ANIE736>3.0.CO