%0 Journal Article
%T Structural basis of LaDR5, a novel agonistic anti-death receptor 5 (DR5) monoclonal antibody, to inhibit DR5/TRAIL complex formation
%A Chunxia Qiao
%A Meiyun Hu
%A Leiming Guo
%A Ming Lv
%A Zhou Lin
%A Jing Geng
%A Xiaoling Lang
%A Xinying Li
%A Yan Li
%A Yuanfang Ma
%A Jiannan Feng
%A Beifen Shen
%J BMC Immunology
%D 2012
%I BioMed Central
%R 10.1186/1471-2172-13-40
%X In this study, we reported a novel mouse anti-human DR5 monoclonal antibody, named as LaDR5, which could compete with TRAIL to bind DR5 and induce the apoptosis of Jurkat cells in the absence of second cross-linking in vitro. Using computer-guided molecular modeling method, the 3-D structure of LaDR5 Fv fragment was constructed. According to the crystal structure of DR5, the 3-D complex structure of DR5 and LaDR5 was modeled using molecular docking method. Based on distance geometry method and intermolecular hydrogen bonding analysis, the key functional domain in DR5 was predicted and the DR5 mutants were designed. And then, three mutants of DR5 was expressed in prokaryotic system and purified by affinity chromatograph to determine the epitope of DR5 identified by LaDR5, which was consistent with the theoretical results of computer-aided analysis.Our results demonstrated the specific epitope located in DR5 that plays a crucial role in antibody binding and even antineoplastic bioactivity. Meanwhile, revealed structural features of DR5 may be important to design or screen novel drugs agonist DR5.
%K TRAIL
%K Death receptor 5
%K Monoclonal antibody
%K Apoptosis
%K Breast cancer
%U http://www.biomedcentral.com/1471-2172/13/40/abstract