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Curr Opin Struct Biol. 2017 Aug;45:17-24. doi: 10.1016/j.sbi.2016.10.018. Epub 2016 Nov 16.

Recent advances in understanding proton coupled peptide transport via the POT family.

Author information

1
Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom. Electronic address: simon.newstead@bioch.ox.ac.uk.

Abstract

The POT family of membrane transporters use the inwardly directed proton electrochemical gradient to drive the uptake of essential nutrients into the cell. Originally discovered in bacteria, members of the family have been found in all kingdoms of life except the archaea. A remarkable feature of the family is their diverse substrate promiscuity. Whereas in mammals and bacteria they are predominantly di- and tri-peptide transporters, in plants the family has diverged to recognize nitrate, plant defence compounds and hormones. This promiscuity has led to the development of peptide-based pro-drugs that use PepT1 and PepT2, the mammalian homologues, to improve oral drug delivery. Recent crystal structures from bacterial and plant members of the family have revealed conserved features of the ligand-binding site and provided insights into post-translational regulation. Here I review the current understanding of transport, ligand promiscuity and regulation within the POT family.

PMID:
27865112
PMCID:
PMC5628733
DOI:
10.1016/j.sbi.2016.10.018
[Indexed for MEDLINE]
Free PMC Article

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