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PMID: 9447240 Published · ppublish English Journal Article Review

Trefoil peptides: from structure to function.

Cellular and molecular life sciences : CMLS ·Vol. 53 ·No. 11-12 ·1997-12-00 ·Pages 888-903

Thim L

Abstract

The unique structure in which six cysteine residues in a sequence of 38 or 39 amino acid residues form three disulphide bonds in a 1-5, 2-4 and 3-6 configuration constitutes the basic elements of a trefoil domain. Today three mammalian trefoil factors (TFF1, TFF2 and TFF3) containing one or two trefoil domains are known. Trefoil factors are usually associated with the mucin layer of the gastrointestinal tract. Early studies on trefoil factors concentrated on structure elucidation and sites of expression in health and disease, whereas studies over the last 3-5 years have focused on the mechanism of action and the search for specific receptors. This review summarises our present knowledge of trefoil peptide structures, their sites of expression, and their protection and repair functions, with a focus on the mechanism by which these peptides exert their biological function.

MeSH Terms
Amino Acid Sequence Animals Cysteine/chemistry Digestive System Physiological Phenomena Growth Substances Humans Intercellular Signaling Peptides and Proteins Intestinal Mucosa/physiology Mice Mice, Transgenic Models, Molecular Molecular Sequence Data Mucins Muscle Proteins Neuropeptides Peptides Proteins Rats Sequence Alignment Sequence Homology, Amino Acid Structure-Activity Relationship Terminology as Topic Trefoil Factor-1 Trefoil Factor-2 Trefoil Factor-3 Tumor Suppressor Proteins
Chemicals
Growth Substances Intercellular Signaling Peptides and Proteins Mucins Muscle Proteins Neuropeptides Peptides Proteins TFF1 protein, human TFF2 protein, human TFF3 protein, rat Tff2 protein, rat Trefoil Factor-1 Trefoil Factor-2 Trefoil Factor-3 Tumor Suppressor Proteins pancreatic spasmolytic polypeptide Cysteine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Thim L
Department of Protein Chemistry, Novo Nordisk A/S, Bagsvaerd, Denmark. [email protected]
Article Info
Journal
Cellular and molecular life sciences : CMLS
Abbr.
Cell Mol Life Sci
ISSN
1420-682X
Published
1997-12-00
Pages
888-903
Language
English
Region
Switzerland
NLM ID
9705402
Subset
IM
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