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Peroxidase-Catalyzed and Photo-Oxidation of Tryptophan Results in Distinct Isomeric Tryptophan Dimers

Year: 2025

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide Heme peroxidases, including horseradish peroxidase (HRP), catalyze the oxidation of a wide variety of substrates by hydrogen peroxide (H 2 O 2 ) via the peroxidase cycle of these enzymes. Oxidation of free tryptophan (Trp) by HRP/H 2 O 2 has been previously reported, but the formation of tryptophan dimers (di-Trp), which are biologically relevant, has not been studied. Here, we report on di-Trp production arising from oxidation of free Trp, at pH 5.5 and 9.2, by HRP/H 2 O 2, as determined by liquid chromatography–mass spectrometry (LC-MS/MS) and selected reaction monitoring (SRM). These data were compared with those from riboflavin-sensitized photo-oxidation, and the products were rationalized by in silico studies. Incubation of varying concentrations of Trp and H 2 O 2 with HRP, irrespective of the pH, resulted in the consumption of ∼2 mol of Trp per mole H 2 O 2 . Formation of multiple di-Trp isomers was detected, using m / z 407 → 203 and m / z 407 → 390 transitions, with greater yields detected at pH 9.2 than 5.5. These results contrast with riboflavin-mediated photo-oxidation where one di-Trp dimer predominated as detected by the m / z 407 → 203 transition. In silico docking studies suggest di-Trp formation within the catalytic pocket of HRP, and subsequent release is a probable mechanism, although other alternative scenarios are also possible.

Source: ACS Omega

DOI: 10.1021/acsomega.5c07535