Published in

American Association for the Advancement of Science, Science, 5691(305), p. 1770-1773, 2004

DOI: 10.1126/science.1101148

Links

Tools

Export citation

Search in Google Scholar

Crystal Structure of a Shark Single-Domain Antibody V Region in Complex with Lysozyme

Journal article published in 2004 by Robyn L. Stanfield ORCID, Helen Dooley, Martin F. Flajnik, Ian A. Wilson
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Green circle
Postprint: archiving allowed
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

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.