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Structural Determination of the Broadly Reactive Anti-IGHV1-69 Anti-idiotypic Antibody G6 and Its Idiotope
Author(s) -
Yuval Avnir,
Kristina Prachanronarong,
Zhen Zhang,
Shurong Hou,
Eric Charles Peterson,
Jianhua Sui,
Hatem Zayed,
Vinodh B. Kurella,
Andrew T. McGuire,
Leonidas Stamatatos,
Brendan Hilbert,
MarkusFrederik Bohn,
Timothy F. Kowalik,
Jeffrey D. Jensen,
Robert W. Finberg,
Jennifer Wang,
Margaret Goodall,
Roy Jefferis,
Quan Zhu,
Neşe Kurt Yılmaz,
Celia A. Schiffer,
Wayne A. Marasco
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.11.056
Subject(s) - idiotopes , germline , idiotype , antibody , biology , immunoglobulin light chain , gene , glycobiology , genetics , monoclonal antibody , glycan , glycoprotein
The heavy chain IGHV1-69 germline gene exhibits a high level of polymorphism and shows biased use in protective antibody (Ab) responses to infections and vaccines. It is also highly expressed in several B cell malignancies and autoimmune diseases. G6 is an anti-idiotypic monoclonal Ab that selectively binds to IGHV1-69 heavy chain germline gene 51p1 alleles that have been implicated in these Ab responses and disease processes. Here, we determine the co-crystal structure of humanized G6 (hG6.3) in complex with anti-influenza hemagglutinin stem-directed broadly neutralizing Ab D80. The core of the hG6.3 idiotope is a continuous string of CDR-H2 residues starting with M53 and ending with N58. G6 binding studies demonstrate the remarkable breadth of binding to 51p1 IGHV1-69 Abs with diverse CDR-H3, light chain, and antigen binding specificities. These studies detail the broad expression of the G6 cross-reactive idiotype (CRI) that further define its potential role in precision medicine.

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