抗体
药品
计算生物学
抗原
配体(生物化学)
体内
药理学
化学
生物
免疫学
生物化学
受体
遗传学
作者
John N. Weinstein,Kenji Fujimori
出处
期刊:Springer eBooks
[Springer Nature]
日期:1990-01-01
卷期号:: 359-370
被引量:6
标识
DOI:10.1007/978-1-4684-5739-1_17
摘要
Antibodies are quintessentially “information macromolecules.” Since the information resides in their antigen-binding sites, it is not surprising that most of the contributions on antibodies in this volume have focused on binding. That is, they have focused on structures and processes that influence the last few nanometers before molecular docking. Here we will consider the prior process, the pharmacokinetic path by which an antibody molecule reaches the proximity of its target antigen. That this perspective is important to the rational design of next-generation ligand molecules should require no argument. Although the title of this chapter emphasizes antibody—drug conjugates, we will focus on generic issues of pharmacology that apply to any of the forms in which antibodies (or, for that matter, other biological ligands) are used in vivo.
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