Recognition of antigens by single domain antibody fragments: the superfluous luxury of paired domains

被引:244
作者
Muyldermans, S
Cambillau, C
Wyns, L
机构
[1] Free Univ Brussels VIB, B-1640 Rhode St Genese, Belgium
[2] CNRS, UMR 6098, Architecture & Fonct Macromol Biol, F-13402 Marseille, France
[3] Univ Aix Marseille 2, F-13402 Marseille 20, France
关键词
D O I
10.1016/S0968-0004(01)01790-X
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 antigen-binding site of antibodies from vertebrates is formed by combining the variable domains of a heavy chain (VH) and a light chain (VL). However, antibodies from camels and Ilamas are an important exception to this in that their sera contain, in addition, a unique kind of antibody that is formed by heavy chains only The antigen-binding site of these antibodies consists of one single domain, referred to as VHH. This article reviews the mutations and structural adaptations th at have ta ken place to reshape a VH of a VH-VL pair into a single-domain VHH with retention of a sufficient variability, The VHH has a potent antigen-binding capacity and provides the advantage of interacting with novel epitopes that are inaccessible to conventional VH-VL pairs.
引用
收藏
页码:230 / 235
页数:6
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