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Protease-resistant peptide design-empowering nature's fragile warriors against HIV.
Weinstock, Matthew T; Francis, J Nicholas; Redman, Joseph S; Kay, Michael S.
Afiliación
  • Weinstock MT; Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT 84112-5650, USA.
Biopolymers ; 98(5): 431-42, 2012.
Article en En | MEDLINE | ID: mdl-23203688
Peptides have great potential as therapeutic agents, but their use is often limited by susceptibility to proteolysis and their resulting in vivo fragility. In this review, we focus on peptidomimetic approaches to produce protease-resistant peptides with the potential for greatly improved clinical utility. We focus on the use of mirror-image (D-peptide) and ß-peptides as two leading approaches with distinct design principles and challenges. Application to the important and difficult problem of inhibiting HIV entry illustrates the current state-of-the-art in peptidomimetic technologies. We also summarize future directions for this field and highlight remaining obstacles to widespread use of protease-resistant peptides.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptido Hidrolasas / Péptidos / Diseño de Fármacos / Infecciones por VIH / Inhibidores de la Proteasa del VIH Límite: Humans Idioma: En Revista: Biopolymers Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptido Hidrolasas / Péptidos / Diseño de Fármacos / Infecciones por VIH / Inhibidores de la Proteasa del VIH Límite: Humans Idioma: En Revista: Biopolymers Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos