Calmodulin selectively modulates the guanylate cyclase activity by repressing the lipid phase separation temperature in the inner half of the bilayer of rat brain synaptosomal plasma membranes.

The association of [125I-]calmodulin with rat brain synaptosomal plasma membranes, when incubated for 1 h at 25 degrees in the presence or in absence of 20 microM Ca2+, follows a sigmoid path with a Hill coefficient h = 1.79 +/- 0.12 and h = 1.72 +/- 0.11, respectively. The total association of calmodulin with the membrane increased approx. 60%-80% at all the range of calmodulin concentrations used in the presence of 20 microM Ca2+. A three fold increase of guanylate cyclase activity was shown in the presence of low concentrations of calmodulin (up to 10 nM); higher concentrations (up to 40 nM) however, led to a progressive inhibition of the enzyme activity with respect to maximal stimulation. Calmodulin increased the lipid fluidity of synaptosomal plasma membranes labeled with 1,6-diphenyl-1,3,5-hexatriene (DPH), as indicated by the steady-state fluorescence anisotropy [(ro/r)-1]-1. Arrhenius-type plots of [(ro/r)-1]-1 indicated that the lipid separation of the membrane at 22.7 +/- 1.2 degrees was perturbed by calmodulin such that the temperature was reduced to 16.3 +/- 0.9 degrees and 15.5 +/- 0.8 degrees in the absence or in the presence of 20 microM Ca2+. Arrhenius plots of guanylate cyclase and acetylcholinesterase activities exhibited break points at 26.7 +/- 1.4 degrees and 22.3 +/- 1.0 degrees in control synaptosomal plasma membranes, respectively. The break point for the guanylate cyclase was reduced to 16.3 +/- 0.9 degrees in calmodulin treated synaptosomal plasma membranes whereas that of acetylcholinesterase remained unaffected (21.1 +/- 0.9 degrees).(ABSTRACT TRUNCATED AT 250 WORDS)