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Blocking peptides and molecular mimicry as treatment for kidney disease.

Authors :
Havasi, Andrea
Weining Lu
Cohen, Herbert T.
Beck, Laurence
Zhiyong Wang
Igwebuike, Chinaemare
Borkan, Steven C.
Source :
American Journal of Physiology: Renal Physiology. Jun2017, Vol. 312 Issue 6, pF1016-F1025. 10p.
Publication Year :
2017

Abstract

Protein mimotopes, or blocking peptides, are small therapeutic peptides that prevent protein-protein interactions by selectively mimicking a native binding domain. Inexpensive technology facilitates straightforward design and production of blocking peptides in sufficient quantities to allow preventive and therapeutic trials in both in vitro and in vivo experimental disease models. The kidney is an ideal peptide target, since small molecules undergo rapid filtration and efficient bulk absorption by tubular epithelial cells. Because the half-life of peptides is markedly prolonged in the kidneys compared with the bloodstream, blocking peptides are an attractive tool for treating diverse renal diseases, including ischemia, proteinuric states, such as membranous nephropathy and focal and segmental glomerulosclerosis, and renal cell carcinoma. Therapeutic peptides represent one of the fastest-growing reagent classes for novel drug development in human disease, partly because of their ease of administration, high binding affinity, and minimal off-target effects. This review introduces the concepts of blocking peptide design, production, and administration and highlights the potential use of therapeutic peptides to prevent or treat specific renal diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1931857X
Volume :
312
Issue :
6
Database :
Academic Search Index
Journal :
American Journal of Physiology: Renal Physiology
Publication Type :
Academic Journal
Accession number :
123509321
Full Text :
https://doi.org/10.1152/ajprenal.00601.2015