Phospholipase C associated with particulate fractions of bovine brain.
Author(s) -
Kuen Yong Lee,
Sung Ho Ryu,
PannGhill Suh,
Wonchul Choi,
Sangkee Rhee
Publication year - 1987
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.84.16.5540
Subject(s) - cytosol , phospholipase c , enzyme , trypsin , biochemistry , phospholipase , chromatography , chemistry , specific activity
We previously reported that cytosolic fractions of bovine brain contain two immunologically distinct phosphoinositide-specific phospholipases C (PLCs), PLC-I and PLC-II. In this report the subcellular distribution of PLC-I and PLC-II in brain homogenates was measured using RIA. Significant differences were found in the distribution of the two forms of PLC in 100,000 X g supernatants (cytosolic fraction) of brain homogenized in hypotonic buffer and 2 M KCl extracts of washed pellets (particulate fraction). More than 90% of PLC-II was found in the cytosolic fractions, whereas the PLC-I-like molecules were equally distributed between cytosolic and particulate fractions. Purification of PLC enzyme to near homogeneity from the particulate fractions yielded two PLC enzymes, both of which could be recognized by anti-PLC-I antibodies but not by anti-PLC-II antibodies. Their Mr values, determined under denaturing conditions, were 150,000 and 140,000. The polypeptide of the enzyme of Mr 150,000 seems to be the same as that of the cytosolic enzyme PLC-I: their Mr values were identical, and their trypsin-digested peptides yielded a similar elution profile on a C18 reverse-phase column. We propose, therefore, that PLC-I and its truncated form are weakly associated with membranes.
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