Natural and engineered kallikrein inhibitors: an emerging pharmacopoeia


Autoria(s): Swedberg, Joakim; De Veer, Simon; Harris, Jonathan
Data(s)

2010

Resumo

The kallikreins and kallikrein-related peptidases are serine proteases that control a plethora of developmental and homeostatic phenomena, ranging from semen liquefaction to skin desquamation and blood pressure. The diversity of roles played by kallikreins has stimulated considerable interest in these enzymes from the perspective of diagnostics and drug design. Kallikreins already have well-established credentials as targets for therapeutic intervention and there is increasing appreciation of their potential both as biomarkers and as targets for inhibitor design. Here, we explore the current status of naturally occurring kallikrein protease-inhibitor complexes and illustrate how this knowledge can interface with strategies for rational re-engineering of bioscaffolds and design of small-molecule inhibitors.

Formato

application/pdf

Identificador

http://eprints.qut.edu.au/42921/

Publicador

Walter de Gruyter GmbH and Co. KG

Relação

http://eprints.qut.edu.au/42921/1/42921.pdf

DOI:10.1515/BC.2010.037

Swedberg, Joakim, De Veer, Simon, & Harris, Jonathan (2010) Natural and engineered kallikrein inhibitors: an emerging pharmacopoeia. Biological Chemistry: official scientific journal of the GBM, 391(4), pp. 357-374.

Direitos

Copyright 2010 Walter de Gruyter

The final publication is available at www.degruyter.com

Fonte

Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #060100 BIOCHEMISTRY AND CELL BIOLOGY #bioscaffold, drug design, inhibitor, phage display, protease positional scanning synthetic combinatorial library, sunflower trypsin inhibitor
Tipo

Journal Article