| Literature DB >> 31612205 |
Dragana Despotović1, Einav Aharon1, Artem Dubovetskyi1, Haim Leader1, Yacov Ashani1, Dan S Tawfik1.
Abstract
Nerve agents are organophosphates (OPs) that potently inhibit acetylcholinesterase, and their enzymatic detoxification has been a long-standing goal. Nerve agents vary widely in size, charge, hydrophobicity and the cleavable ester bond. A single enzyme is therefore unlikely to efficiently hydrolyze all agents. Here, we describe a mixture of three previously developed variants of the bacterial phosphotriesterase (Bd-PTE) that are highly stable and nearly sequence identical. This mixture enables effective detoxification of a broad spectrum of known threat agents-GA (tabun), GB (sarin), GD (soman), GF (cyclosarin), VX and Russian-VX. The potential for dimer dissociation and exchange that could inactivate Bd-PTE has minimal impact, and the three enzyme variants are as active in a mixture as they are individually. To our knowledge, this engineered enzyme 'cocktail' comprises the first solution for enzymatic detoxification of the entire range of threat nerve agents.Entities:
Keywords: enzyme cocktail; organophosphate nerve agents; phosphotriesterase; protein engineering
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Year: 2019 PMID: 31612205 DOI: 10.1093/protein/gzz039
Source DB: PubMed Journal: Protein Eng Des Sel ISSN: 1741-0126 Impact factor: 1.650