Structural diversity of ultralong CDRH3s in seven bovine antibody heavy chains

Jinhui Dong, Jessica A. Finn, Peter A. Larsen, Timothy P.L. Smith, James E. Crowe

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Antigen recognition by mammalian antibodies represents the most diverse setting for protein-protein interactions, because antibody variable regions contain exceptionally diverse variable gene repertoires of DNA sequences containing combinatorial, non-templated junctional mutational diversity. Some animals use additional strategies to achieve structural complexity in the antibody combining site, and one of the most interesting of these is the formation of ultralong heavy chain complementarity determining region 3 loops in cattle. Repertoire sequencing studies of bovine antibody heavy chain variable sequences revealed that bovine antibodies can contain heavy chain complementarity determining region 3 (CDRH3) loops with 60 or more amino acids, with complex structures stabilized by multiple disulfide bonds. It is clear that bovine antibodies can achieve long, peculiarly structured CDR3s, but the range of diversity and complexity of those structures is poorly understood. We determined the atomic resolution structure of seven ultralong bovine CDRH3 loops. The studies, combined with five previous structures, reveal a large diversity of cysteine pairing variations, and highly diverse globular domains.

Original languageEnglish (US)
Article number558
JournalFrontiers in immunology
Volume10
Issue numberMAR
DOIs
StatePublished - 2019

Bibliographical note

Funding Information:
X-ray diffraction data were collected at Beamline 21-ID-G at the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. Use of the LS-CAT Sector 21 was supported by the Michigan Economic Development Corporation and the Michigan Technology Tri-Corridor (Grant 085P1000817). Support for crystallography was provided from the Vanderbilt Center for Structural Biology. The mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture.

Publisher Copyright:
© 2019 Dong, Finn, Larsen, Smith and Crowe. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

Keywords

  • Antigen-antibody recognition
  • Bos taurus
  • Crystal structure
  • Disulfide
  • Lymphocytes
  • Monoclonal antibody
  • Ultralong CDRH3

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