alpha-chymotrypsin and diazobenzenesulfonic-acid

alpha-chymotrypsin has been researched along with diazobenzenesulfonic-acid* in 2 studies

Other Studies

2 other study(ies) available for alpha-chymotrypsin and diazobenzenesulfonic-acid

ArticleYear
Topology of beef heart cytochrome c oxidase from studies on reconstituted membranes.
    Biochemistry, 1984, Nov-06, Volume: 23, Issue:23

    The orientation of purified beef heart cytochrome c oxidase, incorporated into vesicles by the cholate dialysis procedure [Carroll, R.C., & Racker, E. (1977) J. Biol. Chem. 252, 6981], has been investigated by functional and structural approaches. The level of heme reduction obtained by using cytochrome c along with the membrane-impermeant electron donor ascorbate was 78 +/- 2% of that obtained with cytochrome c and the membrane-permeant reagent N,N,N',N'-tetramethyl-p-phenylenediamine. Electron transfer from cytochrome c is known to occur exclusively from the outer surface of the mitochondrial inner membrane (C side), implying that at least 78% of the oxidase molecules are oriented in the same way in these vesicles as in the intact mitochondria. Trypsin, which cleaves subunit IV near its N terminus, modifies only 5-7% of this subunit in intact vesicles. This removal of the N-terminal residues has been shown to occur only in mitochondrial membranes with their inner side (M side) exposed. Diazobenzene [35S]sulfonate [( 35S]DABS) likewise modifies subunit IV only in submitochondrial particles. Labeling of intact membranes with [35S]DABS resulted in incorporation of only 4-8% of the total counts that could be incorporated into this subunit in membranes made leaky to the reagent by addition of 2% Triton X-100. Therefore, both the functional and structural data show that at least 80% and probably more of the cytochrome c oxidase molecules are oriented with their C domain outermost and M domains in the lumen of vesicles prepared by the cholate dialysis method.(ABSTRACT TRUNCATED AT 250 WORDS)

    Topics: Adamantane; Animals; Cattle; Chymotrypsin; Diazonium Compounds; Dicyclohexylcarbodiimide; Electron Transport Complex IV; Heme; Indicators and Reagents; Macromolecular Substances; Membrane Proteins; Mitochondria, Heart; Oxidation-Reduction; Peptide Fragments; Sulfanilic Acids; Trypsin

1984
[Decomposition of chymotrypsin and chymotrypsin derivatives by diazobenzene-sulfonic acid and characterization of "reactive" histidine residues of the active centers].
    Biochemische Zeitschrift, 1962, Volume: 336

    Topics: Azo Compounds; Chymotrypsin; Diazonium Compounds; Histidine; Sulfanilic Acids; Sulfonic Acids; Tyrosine

1962