Mapping Sites in Guanylyl Cyclase Activating Protein-1 Required for Regulation of Photoreceptor Membrane Guanylyl Cyclases
Guanylyl cyclase activating protein (GCAP)-1 regulates photoreceptor membrane guanylyl cyclase, RetGC, in a Ca 2+ -sensitive manner. It contains four Ca 2+ -binding motifs, EF-hands, three of which are capable of binding Ca 2+ . GCAP-1 activates RetGC in low Ca 2+ and inhibits it in high Ca 2+ . In...
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Veröffentlicht in: | The Journal of biological chemistry 1999-04, Vol.274 (16), p.10833-10839 |
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creator | Krylov, D M Niemi, G A Dizhoor, A M Hurley, J B |
description | Guanylyl cyclase activating protein (GCAP)-1 regulates photoreceptor membrane guanylyl cyclase, RetGC, in a Ca 2+ -sensitive manner. It contains four Ca 2+ -binding motifs, EF-hands, three of which are capable of binding Ca 2+ . GCAP-1 activates RetGC in low Ca 2+ and inhibits it in high Ca 2+ . In this study we used deletion and substitution analysis to identify regions of GCAP-1 sequence that are specifically required
for inhibition and activation. A COOH-terminal sequence within Met 157 to Arg 182 is required for activation but not for inhibition of RetGC. We localized one essential stretch to 5 residues from Arg 178 to Arg 182 . Another sequence essential for activation is within the N-terminal residues Trp 21 to Thr 27 . The region between EF-hands 1 and 3 of GCAP-1 also contains elements needed for activation of RetGC. Finally, we found that
inhibition of RetGC requires the first 9 amino-terminal residues of GCAP-1, but none of the residues from Gln 33 to the COOH-terminal Gly 205 are specifically required for inhibition. The ability of GCAP-1 mutants to regulate RetGC was tested on total guanylyl cyclase
activity present in rod outer segments. In addition, the key mutants were also shown to produce similar effects on recombinant
bovine outer segment cyclases GC1 and GC2. |
doi_str_mv | 10.1074/jbc.274.16.10833 |
format | Article |
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for inhibition and activation. A COOH-terminal sequence within Met 157 to Arg 182 is required for activation but not for inhibition of RetGC. We localized one essential stretch to 5 residues from Arg 178 to Arg 182 . Another sequence essential for activation is within the N-terminal residues Trp 21 to Thr 27 . The region between EF-hands 1 and 3 of GCAP-1 also contains elements needed for activation of RetGC. Finally, we found that
inhibition of RetGC requires the first 9 amino-terminal residues of GCAP-1, but none of the residues from Gln 33 to the COOH-terminal Gly 205 are specifically required for inhibition. The ability of GCAP-1 mutants to regulate RetGC was tested on total guanylyl cyclase
activity present in rod outer segments. In addition, the key mutants were also shown to produce similar effects on recombinant
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for inhibition and activation. A COOH-terminal sequence within Met 157 to Arg 182 is required for activation but not for inhibition of RetGC. We localized one essential stretch to 5 residues from Arg 178 to Arg 182 . Another sequence essential for activation is within the N-terminal residues Trp 21 to Thr 27 . The region between EF-hands 1 and 3 of GCAP-1 also contains elements needed for activation of RetGC. Finally, we found that
inhibition of RetGC requires the first 9 amino-terminal residues of GCAP-1, but none of the residues from Gln 33 to the COOH-terminal Gly 205 are specifically required for inhibition. The ability of GCAP-1 mutants to regulate RetGC was tested on total guanylyl cyclase
activity present in rod outer segments. In addition, the key mutants were also shown to produce similar effects on recombinant
bovine outer segment cyclases GC1 and GC2.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Calcium-Binding Proteins - chemistry</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Cattle</subject><subject>Cell Line</subject><subject>Guanylate Cyclase - metabolism</subject><subject>Guanylate Cyclase-Activating Proteins</subject><subject>Humans</subject><subject>Membrane Proteins - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Photoreceptor Cells - metabolism</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - metabolism</subject><subject>Sequence Homology, Amino Acid</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9r2zAYhkVpWbJu956KDqU3p5Js68cxhC4btLS0G-wmZPlLomBbjmSvZH_9lKWHlR2qy8sHz_ci6UHogpIZJaK42VZ2xkQxozzNMs9P0PSQWV7Sn6doSgijmWKlnKCPMW5JOoWiH9CEEqo4LdUU_b43fe-6NX52A0TsOrwcTbdv9g1e7G1jIuC5HdwvMxygx-AHcF1G8RPsRhegxisf0rAem0T4DvsVftz4wQew0KfA99BWwXTwX2_8hM5Wponw-TXP0Y8vt98XX7O7h-W3xfwus7kSQ2YVKFPmJVNMSiGtMEJxwygpVV2TusiVqSWvagFFLiQHIQWVNZfppaUklc3P0fWxtw9-N0IcdOuihaZJt_Jj1FxxoVLnuyAVjDJVsASSI2iDjzHASvfBtSbsNSX6IEYnMTqJ0ZTrv2LSyuVr91i1UP-zcDSRgKsjsHHrzUv6Wl05bzfQvu35A6QDleM</recordid><startdate>19990416</startdate><enddate>19990416</enddate><creator>Krylov, D M</creator><creator>Niemi, G A</creator><creator>Dizhoor, A M</creator><creator>Hurley, J B</creator><general>American Society for Biochemistry and Molecular Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>19990416</creationdate><title>Mapping Sites in Guanylyl Cyclase Activating Protein-1 Required for Regulation of Photoreceptor Membrane Guanylyl Cyclases</title><author>Krylov, D M ; Niemi, G A ; Dizhoor, A M ; Hurley, J B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-c9e9a5352928878c7a796a21059dd0d439ad86bd7e43786e78718d68491580bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Calcium-Binding Proteins - chemistry</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>Cattle</topic><topic>Cell Line</topic><topic>Guanylate Cyclase - metabolism</topic><topic>Guanylate Cyclase-Activating Proteins</topic><topic>Humans</topic><topic>Membrane Proteins - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Photoreceptor Cells - metabolism</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - metabolism</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krylov, D M</creatorcontrib><creatorcontrib>Niemi, G A</creatorcontrib><creatorcontrib>Dizhoor, A M</creatorcontrib><creatorcontrib>Hurley, J B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krylov, D M</au><au>Niemi, G A</au><au>Dizhoor, A M</au><au>Hurley, J B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping Sites in Guanylyl Cyclase Activating Protein-1 Required for Regulation of Photoreceptor Membrane Guanylyl Cyclases</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1999-04-16</date><risdate>1999</risdate><volume>274</volume><issue>16</issue><spage>10833</spage><epage>10839</epage><pages>10833-10839</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Guanylyl cyclase activating protein (GCAP)-1 regulates photoreceptor membrane guanylyl cyclase, RetGC, in a Ca 2+ -sensitive manner. It contains four Ca 2+ -binding motifs, EF-hands, three of which are capable of binding Ca 2+ . GCAP-1 activates RetGC in low Ca 2+ and inhibits it in high Ca 2+ . In this study we used deletion and substitution analysis to identify regions of GCAP-1 sequence that are specifically required
for inhibition and activation. A COOH-terminal sequence within Met 157 to Arg 182 is required for activation but not for inhibition of RetGC. We localized one essential stretch to 5 residues from Arg 178 to Arg 182 . Another sequence essential for activation is within the N-terminal residues Trp 21 to Thr 27 . The region between EF-hands 1 and 3 of GCAP-1 also contains elements needed for activation of RetGC. Finally, we found that
inhibition of RetGC requires the first 9 amino-terminal residues of GCAP-1, but none of the residues from Gln 33 to the COOH-terminal Gly 205 are specifically required for inhibition. The ability of GCAP-1 mutants to regulate RetGC was tested on total guanylyl cyclase
activity present in rod outer segments. In addition, the key mutants were also shown to produce similar effects on recombinant
bovine outer segment cyclases GC1 and GC2.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>10196159</pmid><doi>10.1074/jbc.274.16.10833</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Amino Acid Sequence Animals Calcium-Binding Proteins - chemistry Calcium-Binding Proteins - metabolism Cattle Cell Line Guanylate Cyclase - metabolism Guanylate Cyclase-Activating Proteins Humans Membrane Proteins - metabolism Molecular Sequence Data Photoreceptor Cells - metabolism Recombinant Proteins - chemistry Recombinant Proteins - metabolism Sequence Homology, Amino Acid |
title | Mapping Sites in Guanylyl Cyclase Activating Protein-1 Required for Regulation of Photoreceptor Membrane Guanylyl Cyclases |
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