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PMID: 8839921 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Peptide transporters in the intestine and the kidney.

Annual review of nutrition ·Vol. 16 ·1996-00-00 ·Pages 99-119

Leibach FH, Ganapathy V

Abstract

Even though the existence of a transport process for intact peptides in the brush border membrane of intestinal and renal absorptive epithelial cells has been known for almost three decades, it is only recently that the molecular nature of the proteins responsible for the transport process has been elucidated. Two peptide transporters, PEPT 1 and PEPT 2, have been cloned. The cloned transporters catalyze active transport of intact di- and tripeptides and utilize a transmembrane electrochemical H+ gradient as the driving force. The characteristic of H+ coupling makes PEPT 1 and PEPT 2 unique among the transporters thus far identified in mammalian cells. In addition, the peptide transporters have immediate pharmacologic relevance because a number of peptide-like drugs are recognized as substrates by these transporters. Recently, cultured cell lines of intestinal and renal origin that express PEPT 1 and PEPT 2 have been identified. These cell lines are likely to facilitate studies on the regulatory aspects of the peptide transporters.

MeSH Terms
Animals Biological Transport, Active Carrier Proteins/genetics,metabolism Cloning, Molecular Humans Intestinal Mucosa/metabolism Kidney/metabolism Peptide Transporter 1 Symporters
Chemicals
Carrier Proteins Peptide Transporter 1 SLC15A1 protein, human Symporters hydrogen-coupled oligopeptide transporter PepT2
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Leibach F H
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta 30912-2100, USA.
Ganapathy V
Article Info
Journal
Annual review of nutrition
Abbr.
Annu Rev Nutr
ISSN
0199-9885
Published
1996-00-00
Pages
99-119
Language
English
Region
United States
NLM ID
8209988
Subset
IM
Grants
NIDDK NIH HHS · DK 28389 · United States
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