RP-HPLC reveals the L-cysteine induced degradation of phenylmercuric acetate

Proposed biomolecular mechanism by which PMA targets Cys-residues of the SARS-CoV-2 main protease (M2). • The adverse effects of human exposure to phenylmercury acetate are not understood. • Phenylmercury acetate (PMA) also effectively inhibits SARS-CoV 2. • An RP-HPLC method was employed to study the reaction of L-cysteine with PMA. • A novel Hg-peak eluted which was identified as phenylmercuric cysteinate (PMC). • The mechanism of PMC formation is implicated in the inhibition of SARS-CoV 2.

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Publication Details

Journal
Journal of Inorganic Biochemistry
Published
2025-02-05
DOI
https://doi.org/10.1016/j.jinorgbio.2025.112851
Citations
3
Primary Topic
Porphyrin Metabolism and Disorders
Type
article
Field-Weighted Citation Impact
2.42

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article

RP-HPLC reveals the L-cysteine induced degradation of phenylmercuric acetate

Mohamed A. Attia, Jürgen Gailer
3 citations
Journal of Inorganic Biochemistry
Porphyrin Metabolism and Disorders
2.42
article

RP-HPLC reveals the L-cysteine induced degradation of phenylmercuric acetate

Mohamed A. Attia, Jürgen Gailer
article en
3 citations

Abstract

Proposed biomolecular mechanism by which PMA targets Cys-residues of the SARS-CoV-2 main protease (M2). • The adverse effects of human exposure to phenylmercury acetate are not understood. • Phenylmercury acetate (PMA) also effectively inhibits SARS-CoV 2. • An RP-HPLC method was employed to study the reaction of L-cysteine with PMA. • A novel Hg-peak eluted which was identified as phenylmercuric cysteinate (PMC). • The mechanism of PMC formation is implicated in the inhibition of SARS-CoV 2.

Journal of Inorganic BiochemistryVol. 266
University of Calgary (CA)
University of Calgary
Openalex Percentile: Top 13%
Porphyrin Metabolism and Disorders
2.42
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