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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
32
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pubmed:dateCreated |
1996-9-16
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pubmed:abstractText |
Guanylyl cyclase activator proteins GCAP-1 and GCAP-2 (Dizhoor et al. , 1995, Gorczyca et al., 1995) are members of a recently identified subclass of EF-hand type Ca2+-binding proteins that respond to Ca2+ differently than any other known members of the EF-hand superfamily. GCAPs acquire an activating conformation only in their Ca2+-free form. Free Ca2+ concentrations corresponding to levels in dark-adapted vertebrate photoreceptors inhibit the ability of GCAPs to activate photoreceptor guanylyl cyclases (RetGCs). We studied the effects of mutations that block binding of Ca2+ to the EF-hands of GCAP-2. Unlike other EF-hand proteins, which fail to activate their target when their EF-hands are inactivated by mutations, GCAP-2 with any single EF-hand inactivated remains active and is 3-6 times less sensitive to the inhibitory effect of Ca2+. Inactivation of any two or all three EF-hands produces active forms of GCAP-2 that are insensitive to inhibition by physiological intracellular concentrations of Ca2+. Unexpectedly we also found that activation of RetGCs by a Ca2+-insensitive mutant is inhibited by Ca2+-loaded wild type GCAP-2. We propose the following. 1) GCAP-2 can exist in two extreme functional forms: an apo form that activates RetGCs and a Ca2+-loaded form that blocks activation of RetGCs. 2) All three EF-hands of GCAP-2 contribute to the inhibitory effect of Ca2+. 3) Inactivation of two or three EF-hands is sufficient to shift the "activator-inhibitor" transition outside the physiological range of intracellular free Ca2+.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Guanylate Cyclase,
http://linkedlifedata.com/resource/pubmed/chemical/Guanylate Cyclase-Activating...
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
271
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
19346-50
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8702620-Amino Acid Sequence,
pubmed-meshheading:8702620-Animals,
pubmed-meshheading:8702620-Binding Sites,
pubmed-meshheading:8702620-Calcium,
pubmed-meshheading:8702620-Calcium-Binding Proteins,
pubmed-meshheading:8702620-Cattle,
pubmed-meshheading:8702620-Cell Line,
pubmed-meshheading:8702620-DNA, Complementary,
pubmed-meshheading:8702620-Enzyme Activation,
pubmed-meshheading:8702620-Guanylate Cyclase,
pubmed-meshheading:8702620-Guanylate Cyclase-Activating Proteins,
pubmed-meshheading:8702620-Molecular Sequence Data,
pubmed-meshheading:8702620-Mutagenesis,
pubmed-meshheading:8702620-Photoreceptor Cells,
pubmed-meshheading:8702620-Rats,
pubmed-meshheading:8702620-Sequence Homology, Amino Acid
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pubmed:year |
1996
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pubmed:articleTitle |
Inactivation of EF-hands makes GCAP-2 (p24) a constitutive activator of photoreceptor guanylyl cyclase by preventing a Ca2+-induced "activator-to-inhibitor" transition.
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pubmed:affiliation |
Department of Biochemistry and Howard Hughes Medical Institute, University of Washington School of Medicine, Seattle, Washington 98195-7370, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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