Drug-Target Association Kinetics in Drug Discovery

被引:53
作者
IJzerman, Adriaan P. [1 ]
Guo, Dong [2 ]
机构
[1] Leiden Univ, LACDR, Div Drug Discovery & Safety, POB 9502, NL-2300 RA Leiden, Netherlands
[2] Xuzhou Med Univ, Jiangsu Key Lab New Drug Res & Clin Pharm, 209 Tongshan Rd, Xuzhou 221004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
PROTEIN-COUPLED RECEPTOR; BINDING-KINETICS; RESIDENCE TIME; IN-VIVO; LIGAND-BINDING; LONG; DISSOCIATION; MECHANISM; EFFICACY; PHARMACOLOGY;
D O I
10.1016/j.tibs.2019.04.004
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 important role of ligand-receptor binding kinetics in drug design and discovery is increasingly recognized by the drug research community. Over the past decade, accumulating evidence has shown that optimizing the ligand's dissociation rate constant can lead to desirable duration of in vivo target occupancy and, hence, improved pharmacodynamic properties. However, the association rate constant as a pharmacological principle remains less investigated, whereas it can play an equally important role in the selection of drug candidates. This review provides a compilation and discussion of otherwise scarce and dispersed information on this topic, bringing to light the importance of drug -target association in kinetics-directed drug design and discovery.
引用
收藏
页码:861 / 871
页数:11
相关论文
共 88 条
[51]   Electrostatic influence on the kinetics of ligand binding to acetylcholinesterase - Distinctions between active center ligands and fasciculin [J].
Radic, Z ;
Kirchhoff, PD ;
Quinn, DM ;
McCammon, JA ;
Taylor, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (37) :23265-23277
[52]  
Romanowska J, 2015, THERMODYNAMICS KINET, P211, DOI DOI 10.1002/9783527673025.CH11
[53]   Shielded Hydrogen Bonds as Structural Determinants of Binding Kinetics: Application in Drug Design [J].
Schmidtke, Peter ;
Javier Luque, F. ;
Murray, James B. ;
Barril, Xavier .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (46) :18903-18910
[54]  
Schoop Andreas, 2015, Drug Discov Today Technol, V17, P9, DOI 10.1016/j.ddtec.2015.08.003
[55]   Rapid, electrostatically assisted association of proteins [J].
Schreiber, G ;
Fersht, AR .
NATURE STRUCTURAL BIOLOGY, 1996, 3 (05) :427-431
[56]   Ligand Desolvation Steers On-Rate and Impacts Drug Residence Time of Heat Shock Protein 90 (Hsp90) Inhibitors [J].
Schuetz, Doris A. ;
Richter, Lars ;
Arnaral, Marta ;
Grandits, Melanie ;
Graedler, Ulrich ;
Musil, Djordje ;
Buchstaller, Hans-Peter ;
Eggenweiler, Hans-Michael ;
Frech, Matthias ;
Ecker, Gerhard F. .
JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (10) :4397-4411
[57]   Kinetics for Drug Discovery: an industry-driven effort to target drug residence time [J].
Schuetz, Doris A. ;
de Witte, Wilhelmus Egbertus Arnout ;
Wong, Yin Cheong ;
Knasmueller, Bernhard ;
Richter, Lars ;
Kokh, Daria B. ;
Sadiq, S. Kashif ;
Bosma, Reggie ;
Nederpelt, Indira ;
Heitman, Laura H. ;
Segala, Elena ;
Amaral, Marta ;
Guo, Dong ;
Andres, Dorothee ;
Georgi, Victoria ;
Stoddart, Leigh A. ;
Hill, Steve ;
Cooke, Robert M. ;
De Graaf, Chris ;
Leurs, Rob ;
Frech, Matthias ;
Wade, Rebecca C. ;
de Lange, Elizabeth Cunera Maria ;
IJzerman, Adriaan P. ;
Mueller-Fahrnow, Anke ;
Ecker, Gerhard F. .
DRUG DISCOVERY TODAY, 2017, 22 (06) :896-911
[58]  
Shaw D., 2009, Proceedings of the Conference on High Performance Computing Networking, Storage and Analysis (SC09), P65
[59]   Elucidation of HIV-1 protease resistance by characterization of interaction kinetics between inhibitors and enzyme variants [J].
Shuman, CF ;
Markgren, PO ;
Hämäläinen, M ;
Danielson, UH .
ANTIVIRAL RESEARCH, 2003, 58 (03) :235-242
[60]  
Smoluchowski M., 1918, Zeitschrift fr Physikalische Chemie, V92U, P129, DOI [10.1515/zpch-1918-9209, DOI 10.1515/ZPCH-1918-9209]