An Update on Arginase Inhibitors and Inhibitory Assays

Author:

Muller Jason1ORCID,Attia Rym1ORCID,Zedet Andy1ORCID,Girard Corine1ORCID,Pudlo Marc1ORCID

Affiliation:

1. PEPITE EA4267, Université de Bourgogne Franche-Comté, F-25030 Besançon, France

Abstract

Abstract: Arginase, which converts arginine into ornithine and urea, is a promising therapeutic target. Arginase is involved in cardiovascular diseases, parasitic infections and, through a critical role in immunity, in some cancers. There is a need to develop effective arginase inhibitors and therefore efforts to identify and optimize new inhibitors are increasing. Several methods of evaluating arginase activity are available, but few directly measure the product. Radiometric assays need to separate urea and dying reactions require acidic conditions and sometimes heating. Hence, there are a variety of different approaches available, and each approach has its own limits and benefits. In this review, we provide an update on arginase inhibitors, followed by a discussion on available arginase assays and alternative methods, with a focus on the intrinsic biases and parameters that are likely to impact results.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology,General Medicine

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