Artigo Acesso aberto Revisado por pares

Selective and facile assay of human immunodeficiency virus protease activity by a novel fluorogenic reaction

2009; Elsevier BV; Volume: 397; Issue: 2 Linguagem: Inglês

10.1016/j.ab.2009.10.030

ISSN

1096-0309

Autores

Zhi‐Qiang Yu, Tsutomu Kabashima, Chenhong Tang, Takayuki Shibata, Kaio Kitazato, Nobuyuki Kobayashi, Myung Koo Lee, Masaaki Kai,

Tópico(s)

HIV-related health complications and treatments

Resumo

A highly selective and facile assay of human immunodeficiency virus protease (HIV-PR) has been required for the screening of medicinal inhibitors and also for classifying the subtypes of HIV in the therapeutic treatment of acquired immune deficiency syndrome (AIDS). This article describes a novel assay method of HIV-PR based on the selective fluorogenic reaction of peptides. A peptide fragment generated from a substrate by the enzymatic digestion with HIV-PR could be selectively quantified by the spectrofluorometric detection after the fluorogenic reaction with catechol in the presence of sodium periodate and sodium borate (pH 7.0). This assay system uses an N-terminal acetyl peptide as the substrate and crude extracts from Escherichia coli expressing recombinant HIV-PR. The activity obtained by the proposed assay correlated with that obtained by a conventional HIV-PR assay based on fluorescence resonance energy transfer detection.

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