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.
Original language | English |
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Pages (from-to) | 169-174 |
Number of pages | 6 |
Journal | Protein Engineering, Design and Selection |
Volume | 32 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2019 |
Funding
We gratefully acknowledge financial support from Defense Threat Reduction Agency (DTRA) of the US Department of Defense (HDTRA1-17-0057). D.S.T. is the Nella and Leon Benoziyo Professor of Biochemistry. We are grateful to Kesava Phaneendra Cherukuri for assistance in making Fig. 1. Financial support by the Defense Threat Reduction Agency (DTRA) of the US Department of Defense (HDTRA1-17-0057).
All Science Journal Classification (ASJC) codes
- Biotechnology
- Bioengineering
- Biochemistry
- Molecular Biology