溶菌酶
抗体
免疫球蛋白结构域
抗原
生物
免疫球蛋白轻链
免疫系统
单域抗体
互补决定区
抗原抗体复合物
结合位点
化学
生物物理学
生物化学
免疫学
作者
Robyn L. Stanfield,Helen Dooley,Martin F. Flajnik,Ian A. Wilson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-08-20
卷期号:305 (5691): 1770-1773
被引量:284
标识
DOI:10.1126/science.1101148
摘要
Cartilaginous fish are the phylogenetically oldest living organisms known to possess components of the vertebrate adaptive immune system. Key to their immune response are heavy-chain, homodimeric immunoglobulins called new antigen receptors (IgNARs), in which the variable (V) domains recognize antigens with only a single immunoglobulin domain, akin to camelid heavy-chain V domains. The 1.45 angstrom resolution crystal structure of the type I IgNAR V domain in complex with hen egg-white lysozyme (HEL) reveals a minimal antigen-binding domain that contains only two of the three conventional complementarity-determining regions but still binds HEL with nanomolar affinity by means of a binding interface comparable in size to conventional antibodies.
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