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Structure-guided discovery of a single-domain antibody agonist against human apelin receptor
Author(s) -
Yanbin Ma,
Yao Ding,
Xianqiang Song,
Xiaochuan Ma,
Xun Li,
Ning Zhang,
Yunpeng Song,
Yaping Sun,
Yuqing Shen,
Wenge Zhong,
Liaoyuan A. Hu,
Yingli Ma,
Mei-Yun Zhang
Publication year - 2020
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aax7379
Subject(s) - agonist , apelin , drug discovery , receptor , antibody , pharmacology , computational biology , chemistry , medicine , biology , immunology , biochemistry
Developing antibody agonists targeting the human apelin receptor (APJ) is a promising therapeutic approach for the treatment of chronic heart failure. Here, we report the structure-guided discovery of a single-domain antibody (sdAb) agonist JN241-9, based on the cocrystal structure of APJ with an sdAb antagonist JN241, the first cocrystal structure of a class A G protein-coupled receptor (GPCR) with a functional antibody. As revealed by the structure, JN241 binds to the extracellular side of APJ, makes critical contacts with the second extracellular loop, and inserts the CDR3 into the ligand-binding pocket. We converted JN241 into a full agonist JN241-9 by inserting a tyrosine into the CDR3. Modeling and molecular dynamics simulation shed light on JN241-9-stimulated receptor activation, providing structural insights for finding agonistic antibodies against class A GPCRs.

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