Tummino Peter J, Copeland Robert A
Department of Enzymology and Mechanistic Pharmacology and Department of Oncology Biology, Oncology Center of Excellence in Drug Discovery, GlaxoSmithKline, 1250 South Collegeville Road, Collegeville, Pennsylvania 19426, USA.
Biochemistry. 2008 May 20;47(20):5481-92. doi: 10.1021/bi8002023. Epub 2008 Apr 16.
The formation and duration of binary receptor-ligand complexes are fundamental to many physiologic processes. Most often, the effectiveness of interaction between a receptor and its ligand is quantified in terms of closed system, equilibrium affinity measurements, such as IC50 and Kd. In the context of in vivo biology, however, the extent and duration of responses to receptor-ligand interactions depend greatly on the time period over which the ligand is in residence on its receptor. Here we define receptor-ligand complex residence time in quantitative terms and describe its significance to biological function. Examples of the importance of residence time are presented for natural ligands of different receptor types. The impact of residence time on the optimization of potential ligands as drugs for human medicine is also described.
二元受体 - 配体复合物的形成和持续时间是许多生理过程的基础。大多数情况下,受体与其配体之间相互作用的有效性是根据封闭系统中的平衡亲和力测量来量化的,例如IC50和Kd。然而,在体内生物学背景下,对受体 - 配体相互作用的反应程度和持续时间很大程度上取决于配体在其受体上停留的时间段。在这里,我们从定量角度定义受体 - 配体复合物的停留时间,并描述其对生物学功能的重要性。针对不同受体类型的天然配体,给出了停留时间重要性的实例。还描述了停留时间对优化潜在配体作为人类药物的影响。