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. 2022 Oct 17;57:102514. doi: 10.1016/j.redox.2022.102514

Table 1.

Cysteine persulfide (CysSSH) and cysteine polysulfide (CysSSSH) generated by the reaction of cysteine (CysSH) or cystine (CysSSCys) with sulfur donors.

Na2S CysSH (μM) CysSSH (μM) CysSSSH (μM)
100 μM CysSH 74.8 ± 3.5 N.D. N.D.
+ 74.1 ± 2.5 2.2 ± 0.3 N.D.
100 μM CysSSCys
N.D. N.D. N.D.
+
15.6 ± 0.1
22.2 ± 1.2
N.D.
Na2S4 CysSH (μM) CysSSH (μM) CysSSSH (μM)

100 μM CysSH 78.1 ± 1.8 2.0 ± 1.7 N.D.
+ 7.9 ± 1.4 64.7 ± 0.7 34.3 ± 1.1
100 μM CysSSCys N.D. N.D. N.D.
+ 7.3 ± 0.6 65.7 ± 7.6 41.8 ± 3.7

Note: One-hundred micromolar Na2S or Na2S4 was incubated with 100 μM CysSH or CysSSCys in 50 mM HEPES (pH 7.5) at 37°C for 30 min. The reaction mixture was incubated with 1 mM β-(4-hydroxyphenyl)ethyl (HPE) iodoacetamide at 37°C for 30 min to obtain HPE acetamide adducts, which were identified using LC/MS/MS and quantified using isotope-labeled internal standards. N.D., not detected.