TY - JOUR
T1 - Phosphatidic acid and polyphosphoinositide formation in a broken cell preparation from rat brain
T2 - effects of different incubation conditions
AU - Bothmer, J.
AU - Markerink, M.
AU - Jolles, J.
PY - 1990/1/1
Y1 - 1990/1/1
N2 - The formation of phosphatidic acid (PA) and polyphosphoinositides in rat brains in vitro was studied under hypotonic conditions by incubating a lysed crude synaptosomal fraction with [.gamma.-32P]ATP for 10 s. Only phosphatidic acid, phosphatidylinositol-4-phosphate (PIP) and phosphatidylinositol-4,5-bisphosphate (PIP2) were labelled. The formation of PIP2 decreased with increasing preincubation times. PIP and PA formation, however, were not affected. The rate of phosphorylation of PIP, PIP2 and PA was linear with incubation time for at least 10 s, indicating that the ATP/enzyme ratio was sufficiently high. The maximal incorporation of phosphate into the three phospholipids was found at 30.degree.C. Ten millimolar Mg2+ and pH 6.5 were the best compromise for measuring the incorporation of phosphate into PIP, PIP2 and PA simultaneously. A sodium acetate-magnesium acetate buffer system gave optimal kinase activities. The results obtained show that, with minor adjustments of the incubation conditions, it is possible to measure simultaneously the formation of PIP, PIP2 and PA.
AB - The formation of phosphatidic acid (PA) and polyphosphoinositides in rat brains in vitro was studied under hypotonic conditions by incubating a lysed crude synaptosomal fraction with [.gamma.-32P]ATP for 10 s. Only phosphatidic acid, phosphatidylinositol-4-phosphate (PIP) and phosphatidylinositol-4,5-bisphosphate (PIP2) were labelled. The formation of PIP2 decreased with increasing preincubation times. PIP and PA formation, however, were not affected. The rate of phosphorylation of PIP, PIP2 and PA was linear with incubation time for at least 10 s, indicating that the ATP/enzyme ratio was sufficiently high. The maximal incorporation of phosphate into the three phospholipids was found at 30.degree.C. Ten millimolar Mg2+ and pH 6.5 were the best compromise for measuring the incorporation of phosphate into PIP, PIP2 and PA simultaneously. A sodium acetate-magnesium acetate buffer system gave optimal kinase activities. The results obtained show that, with minor adjustments of the incubation conditions, it is possible to measure simultaneously the formation of PIP, PIP2 and PA.
U2 - 10.1016/0197-0186(90)90064-Z
DO - 10.1016/0197-0186(90)90064-Z
M3 - Article
SN - 0197-0186
VL - 17
SP - 27
EP - 33
JO - Neurochemistry International
JF - Neurochemistry International
IS - 1
ER -