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PMID: 11295555 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Recognition of antigens by single-domain antibody fragments: the superfluous luxury of paired domains.

Trends in biochemical sciences ·Vol. 26 ·No. 4 ·2001-04-00 ·Pages 230-5

Muyldermans S, Cambillau C, Wyns L

Abstract

The antigen-binding site of antibodies from vertebrates is formed by combining the variable domains of a heavy chain (VH) and a light chain (VL). However, antibodies from camels and llamas are an important exception to this in that their sera contain, in addition, a unique kind of antibody that is formed by heavy chains only. The antigen-binding site of these antibodies consists of one single domain, referred to as VHH. This article reviews the mutations and structural adaptations that have taken place to reshape a VH of a VH-VL pair into a single-domain VHH with retention of a sufficient variability. The VHH has a potent antigen-binding capacity and provides the advantage of interacting with novel epitopes that are inaccessible to conventional VH-VL pairs.

MeSH Terms
Amino Acid Sequence Antigen-Antibody Reactions Binding Sites, Antibody Complementarity Determining Regions Humans Immunoglobulin Fragments/chemistry,immunology Molecular Sequence Data Protein Conformation Sequence Homology, Amino Acid
Chemicals
Complementarity Determining Regions Immunoglobulin Fragments
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Muyldermans S
Vrije Universiteit Brussel, Vlaams Interuniversitair Instituut Biotechnologie, 65, B-1640 Sint Genesius Rode, Paardenstraat, Belgium. svmuylde@vub.ac.be
Cambillau C
Wyns L
Article Info
Journal
Trends in biochemical sciences
Abbr.
Trends Biochem Sci
ISSN
0968-0004
Published
2001-04-00
Pages
230-5
Language
English
Region
England
NLM ID
7610674
Subset
IM
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