PEST sequences in calmodulin-binding proteins

1995 ◽  
pp. 17-27 ◽  
Author(s):  
Junor A. Barnes ◽  
Aldrin V. Gomes
Keyword(s):  
Binding Proteins ◽  
Calmodulin Binding

Calcium binding to complexes of calmodulin and calmodulin binding proteins

Biochemistry ◽  
1985 ◽  
Vol 24 (27) ◽  
pp. 8081-8086 ◽  
Author(s):  
Bradley B. Olwin ◽  
Daniel R. Storm
Keyword(s):  
Calcium Binding ◽  
Binding Proteins ◽  
Calmodulin Binding

Stimulation of Calmodulin Binding to Skeletal Muscle Membrane Proteins by 1,25-Dihydroxy-Vitamin D 3

1990 ◽  
Vol 45 (6) ◽  
pp. 663-670 ◽  
Author(s):  
Virginia Massheimer ◽  
Luis M. Fernandez ◽  
Ana R. de Boland
Keyword(s):  
Skeletal Muscle ◽  
Vitamin D ◽  
Membrane Proteins ◽  
Binding Proteins ◽  
Sodium Dodecyl ◽  
Muscle Membrane ◽  
Calmodulin Binding ◽  
Ca Uptake ◽  
Vitamin D 3 ◽  
Stimulation Of

Abstract Previous work has shown that 1,25-dihydroxy-vitamin D 3 rapidly increases calmodulin levels of skeletal muscle membranes without altering the muscle cell calmodulin content. Therefore, the effects of the sterol on the binding of calmodulin to specific muscle membrane proteins were investigated. Soleus muscles from vitamin D-deficient chicks were treated in vitro for short intervals (5-15 min) with physiological concentrations of 1,25-dihydroxy-vitamin D3. Proteins of mitochondria and microsomes isolated by differential centrifugation were separated on sodium dodecyl sulfate polyacrylamide gels. Calmodulin-binding proteins were identified by a [125I]calmodulin gel overlay procedure followed by autoradiography. 1,25-Dihydroxy- vitamin D3 increased the binding of labelled calmodulin to a major, calcium-independent, calmodulin-binding protein of 28 Kda localized in microsomes, and to minor calmodulin- binding proteins of 78 and 130 Kda proteins localized in mitochondria. The binding of [125I]calmodulin to these proteins was abolished by flufenazine or excess non-radioactive calmodulin. 1,25-Dihydroxy-vitamin D3 rapidly increased muscle tissue Ca uptake and cyclic AM P levels and stimulated the phosphorylation of several membrane proteins including those whose calmodulin-binding capacity potentiates. Analogously to the sterol, forskolin increased membrane calmodulin content, calmodulin binding to the 28 Kda microsomal protein and 45Ca uptake by soleus muscle preparations. Forskolin also induced a similar profile of changes in muscle membrane protein phosphorylation as the hormone. These results suggest that 1,25- dihydroxy-vitamin D 3 affects calmodulin distribution in muscle cells through cyclic AMP-dependent phosphorylation of membrane calmodulin-binding proteins. These changes may play a role in the stimulation of muscle Ca uptake by the sterol.

Isolation of brain Ca2+-calmodulin tubulin kinase containing calmodulin binding proteins

1982 ◽  
Vol 108 (1) ◽  
pp. 421-428 ◽  
Author(s):  
James R. Goldenring ◽  
Basilio Gonzalez ◽  
Robert J. DeLorenzo
Keyword(s):  
Binding Proteins ◽  
Calmodulin Binding

Calmodulin-Binding Proteins in a Cloned Rat Insulinoma Cell Line

Diabetes ◽  
1983 ◽  
Vol 32 (12) ◽  
pp. 1126-1133 ◽  
Author(s):  
T. Y. Nelson ◽  
J. M. Oberwetter ◽  
J. G. Chafouleas ◽  
A. E. Boyd
Keyword(s):  
Cell Line ◽  
Binding Proteins ◽  
Calmodulin Binding ◽  
Insulinoma Cell ◽  
Insulinoma Cell Line ◽  
Rat Insulinoma Cell Line ◽  
Rat Insulinoma
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