作者: Y. Ando , M. Steiner
DOI: 10.1016/0005-2736(73)90251-4
关键词: Adduct 、 Reagent 、 Sodium dodecyl sulfate 、 Chromatography 、 Urea 、 Membrane 、 Membrane protein 、 Nitrocellulose 、 Chemistry 、 Thiol 、 Biophysics 、 Cell biology 、 Biochemistry
摘要: Methods were evaluated for the quantitative measurement of free thiols in isolated platelet membranes. Two techniques found applicable utilizing either retentative capacity nitrocellulose filters 203Hg-labeled p-chloromercuri-benzoate adducts membrane proteins or spectrophotometric assay thiol thione anions released formation mixed disulfides between and disulfide reagents, 5,5′-dithiobis(2-nitrobenzoic acid) 6,6′-dithio-dinicotinic acid. Complete partial solubilization membranes with urea, sodium dodecyl sulfate phospholipase A resulted exposure additional to reaction 6,6′-dithiodinicotinic Approximately one half total was be masked native non-solubilized Kinetic studies on rates various SH reagents tested indicate presence at least two classes membrane. The reproducibility simplicity methods proved their general usefulness qualitative assays proteins.