Retinal membrane guanylyl cyclase (RetGC) and Ca2+/Mg2+ sensor proteins (GCAPs) control the recovery of the photoresponse in vertebrate photoreceptors, through their molecular interactions that remain rather poorly understood and controversial. Here we have determined the main RetGC isozyme (RetGC1):GCAP1 binding stoichiometry at Saturation in cyto, using fluorescently labeled RetGC1 and GCAP1 coexpressed in HEK293 cells. In a striking manner, the equimolar binding of RetGC1 with GCAP1 in transfected HEK293 cells typical for wild-type RetGC1 was eliminated by a substitution, D639Y, in the kinase homology domain of RetGC1 found in a patient with a severe form of retinal dystrophy, Leber congenital amaurosis (LCA). A similar effect was observed with another LCA-related mutation, R768W, in the same domain of RetGC1. In contrast to the completely suppressed binding and activation of RetGC1 by Mg2+-liganded GCAP1, neither of these two mutations eliminated the GCAP1-independent activity of RetGC stimulated by Mn2+. These results directly implicate the D639 (and possibly R768)-containing portion of the RetGC1 kinase homology domain in its primary recognition by the Mg2+-bound activator form of GCAP1.
Activation of Retinal Guanylyl Cyclase RetGC1 by GCAP1: Stoichiometry of Binding and Effect of New LCA-Related Mutations
Creators
Igor V. Peshenko - Salus University
Elena V. Olshevskaya - Salus University
Suxia Yao - University of Alabama at Birmingham
Hany H. Ezzeldin - University of Alabama at Birmingham
Steven J. Pittler - University of Alabama at Birmingham
Alexander M. Dizhoor - Salus University
Publication Details
Biochemistry (Easton), v 49(4), pp 709-717
Publisher
Amer Chemical Soc
Number of pages
9
Grant note
Pennsylvania Department of Health
Pennsylvania Lions Sight Conservation and Eye Research Foundation
Foundation Fighting Blindness
EY11522; EY09924; EY018143 / National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
Resource Type
Journal article
Language
English
Academic Unit
Neurobiology and Anatomy; Pennsylvania College of Optometry (PCO)
Web of Science ID
WOS:000273831500007
Scopus ID
2-s2.0-75149139527
Other Identifier
991022035259104721
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