Protein-bound sulfhydryl groups and thiolesters in mitochondria and submitochondrial particles and their relationships to oxidative phosphorylation

Procedures are described for measurement of total protein-bound —SH groups and apparent thiolester linkages in mitochondrial preparations. The procedure for total —SH is based on reaction with radioactive p-mercuribenzoate in 6 m guanidine hydrochloride at pH 9 containing 1 m ammonia buffer. The procedure for apparent thiolesters is based on alkylation of available — SH groups in 6 m guanidine hydrochloride, protein precipitation with perchloric acid, and ammonolysis at pH 9 to liberate — SH from any thiolester present. No variations in total —SH groups measured in Submitochondrial particles or in mitochondria were noted with presence or absence of ATP, ADP, substrates, or uncouplers of oxidative phosphorylation. Previous reports of changes in measured — SH groups thus appear to reflect solely changes in the reactivity of — SH groups and not in the total — SH groups present. Submitochondrial particles contained less than 0.5 nmole of apparent thiolester per mg of protein; mitochondria contained 1 to 2 nmoles. No variation of apparent thiolester content was noted with change in conditions affecting oxidative phosphorylation. The data do not, of course, eliminate possible changes in thiolester content below the sensitivity of the detection procedures.