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Rapid kinetics of calcium dissociation from plant calmodulin and calmodulin-like proteins and effect of target peptides
Calcium (Ca2+) signaling represents a universal information code in plants, playing crucial roles spanning developmental processes to stress responses. Ca2+ signals are decoded into defined plant adaptive responses by different Ca2+ sensing proteins, including calmodulin (CaM) and calmodulin-like (C...
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Published in: | Biochemical and biophysical research communications 2022-01, Vol.590, p.103-108 |
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description | Calcium (Ca2+) signaling represents a universal information code in plants, playing crucial roles spanning developmental processes to stress responses. Ca2+ signals are decoded into defined plant adaptive responses by different Ca2+ sensing proteins, including calmodulin (CaM) and calmodulin-like (CML) proteins. Although major advances have been achieved in describing how these Ca2+ decoding proteins interact and regulate downstream target effectors, the molecular details of these processes remain largely unknown. Herein, the kinetics of Ca2+ dissociation from a conserved CaM and two CML isoforms from A. thaliana has been studied by fluorescence stopped-flow spectroscopy. Kinetic data were obtained for the isolated Ca2+-bound proteins as well as for the proteins complexed with different target peptides. Moreover, the lobe specific interactions between the Ca2+ sensing proteins and their targets were characterized by using a panel of protein mutants deficient in Ca2+ binding at the N-lobe or C-lobe. Results were analyzed and discussed in the context of the Ca2+-decoding and Ca2+-controlled target binding mechanisms in plants.
•Ca2+-binding proteins are instrumental in the control of Ca2+ signaling in plants.•The Arabidopsis genome harbours seven calmodulin and 50 calmodulin-like genes.•We measured Ca2+ dissociation rates from AtCaM1, AtCML7 and AtCML19 by rapid kinetics.•CaM and CML proteins show lobe specific Ca2+ dissociation kinetics.•Peptide binding impacts the kinetic properties of Ca2+-binding sites. |
doi_str_mv | 10.1016/j.bbrc.2021.12.077 |
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•Ca2+-binding proteins are instrumental in the control of Ca2+ signaling in plants.•The Arabidopsis genome harbours seven calmodulin and 50 calmodulin-like genes.•We measured Ca2+ dissociation rates from AtCaM1, AtCML7 and AtCML19 by rapid kinetics.•CaM and CML proteins show lobe specific Ca2+ dissociation kinetics.•Peptide binding impacts the kinetic properties of Ca2+-binding sites.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2021.12.077</identifier><identifier>PMID: 34974297</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Arabidopsis - drug effects ; Arabidopsis - metabolism ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Calcium ; Calcium - metabolism ; Calmodulin ; Calmodulin - metabolism ; Calmodulin-like proteins ; Kinetics ; Melitten - pharmacology ; Melittin ; Mutant Proteins - metabolism ; Peptides - metabolism ; RAD4 ; Rapid kinetics ; SAC3B</subject><ispartof>Biochemical and biophysical research communications, 2022-01, Vol.590, p.103-108</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-8874945055df0eb2f2ea212b1e5f34967fd2d95ca52cb96ae5b14465a783372c3</citedby><cites>FETCH-LOGICAL-c356t-8874945055df0eb2f2ea212b1e5f34967fd2d95ca52cb96ae5b14465a783372c3</cites><orcidid>0000-0002-3902-3512 ; 0000-0002-5921-7365 ; 0000-0002-7341-0970</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34974297$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Troilo, Francesca</creatorcontrib><creatorcontrib>Pedretti, Marco</creatorcontrib><creatorcontrib>Travaglini-Allocatelli, Carlo</creatorcontrib><creatorcontrib>Astegno, Alessandra</creatorcontrib><creatorcontrib>Di Matteo, Adele</creatorcontrib><title>Rapid kinetics of calcium dissociation from plant calmodulin and calmodulin-like proteins and effect of target peptides</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Calcium (Ca2+) signaling represents a universal information code in plants, playing crucial roles spanning developmental processes to stress responses. Ca2+ signals are decoded into defined plant adaptive responses by different Ca2+ sensing proteins, including calmodulin (CaM) and calmodulin-like (CML) proteins. Although major advances have been achieved in describing how these Ca2+ decoding proteins interact and regulate downstream target effectors, the molecular details of these processes remain largely unknown. Herein, the kinetics of Ca2+ dissociation from a conserved CaM and two CML isoforms from A. thaliana has been studied by fluorescence stopped-flow spectroscopy. Kinetic data were obtained for the isolated Ca2+-bound proteins as well as for the proteins complexed with different target peptides. Moreover, the lobe specific interactions between the Ca2+ sensing proteins and their targets were characterized by using a panel of protein mutants deficient in Ca2+ binding at the N-lobe or C-lobe. Results were analyzed and discussed in the context of the Ca2+-decoding and Ca2+-controlled target binding mechanisms in plants.
•Ca2+-binding proteins are instrumental in the control of Ca2+ signaling in plants.•The Arabidopsis genome harbours seven calmodulin and 50 calmodulin-like genes.•We measured Ca2+ dissociation rates from AtCaM1, AtCML7 and AtCML19 by rapid kinetics.•CaM and CML proteins show lobe specific Ca2+ dissociation kinetics.•Peptide binding impacts the kinetic properties of Ca2+-binding sites.</description><subject>Arabidopsis - drug effects</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Calcium</subject><subject>Calcium - metabolism</subject><subject>Calmodulin</subject><subject>Calmodulin - metabolism</subject><subject>Calmodulin-like proteins</subject><subject>Kinetics</subject><subject>Melitten - pharmacology</subject><subject>Melittin</subject><subject>Mutant Proteins - metabolism</subject><subject>Peptides - metabolism</subject><subject>RAD4</subject><subject>Rapid kinetics</subject><subject>SAC3B</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kEFrFTEUhYMo9rX6B7qQLN3MmGQmyQt0U4raQkEQBXchk9yUvM5MxiRT8d-b6avSlavL5Z5zuOdD6JySlhIqPhzaYUi2ZYTRlrKWSPkC7ShRpGGU9C_RjhAiGqbojxN0mvOBEEp7oV6jk65XsmdK7tCvr2YJDt-HGUqwGUePrRltWCfsQs7RBlNCnLFPccLLaOay3afo1jHM2Mzu2dqM4R7wkmKBMOfHI3gPtmypxaQ7KHiBpQQH-Q165c2Y4e3TPEPfP338dnXd3H75fHN1edvYjovS7PeyVz0nnDtPYGCegWGUDRS4ryWE9I45xa3hzA5KGOAD7XvBjdx3nWS2O0Pvj7n1rZ8r5KKnkC2MtQnENWsmqGByL1VXpewotSnmnMDrJYXJpN-aEr0B1we9AdcbcE2ZrsCr6d1T_jpM4P5Z_hKugoujAGrLhwBJZxtgtuBCqmi0i-F_-X8AvQGTYg</recordid><startdate>20220129</startdate><enddate>20220129</enddate><creator>Troilo, Francesca</creator><creator>Pedretti, Marco</creator><creator>Travaglini-Allocatelli, Carlo</creator><creator>Astegno, Alessandra</creator><creator>Di Matteo, Adele</creator><general>Elsevier Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0002-3902-3512</orcidid><orcidid>https://orcid.org/0000-0002-5921-7365</orcidid><orcidid>https://orcid.org/0000-0002-7341-0970</orcidid></search><sort><creationdate>20220129</creationdate><title>Rapid kinetics of calcium dissociation from plant calmodulin and calmodulin-like proteins and effect of target peptides</title><author>Troilo, Francesca ; Pedretti, Marco ; Travaglini-Allocatelli, Carlo ; Astegno, Alessandra ; Di Matteo, Adele</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-8874945055df0eb2f2ea212b1e5f34967fd2d95ca52cb96ae5b14465a783372c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Arabidopsis - drug effects</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Calcium</topic><topic>Calcium - metabolism</topic><topic>Calmodulin</topic><topic>Calmodulin - metabolism</topic><topic>Calmodulin-like proteins</topic><topic>Kinetics</topic><topic>Melitten - pharmacology</topic><topic>Melittin</topic><topic>Mutant Proteins - metabolism</topic><topic>Peptides - metabolism</topic><topic>RAD4</topic><topic>Rapid kinetics</topic><topic>SAC3B</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Troilo, Francesca</creatorcontrib><creatorcontrib>Pedretti, Marco</creatorcontrib><creatorcontrib>Travaglini-Allocatelli, Carlo</creatorcontrib><creatorcontrib>Astegno, Alessandra</creatorcontrib><creatorcontrib>Di Matteo, Adele</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Troilo, Francesca</au><au>Pedretti, Marco</au><au>Travaglini-Allocatelli, Carlo</au><au>Astegno, Alessandra</au><au>Di Matteo, Adele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid kinetics of calcium dissociation from plant calmodulin and calmodulin-like proteins and effect of target peptides</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2022-01-29</date><risdate>2022</risdate><volume>590</volume><spage>103</spage><epage>108</epage><pages>103-108</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Calcium (Ca2+) signaling represents a universal information code in plants, playing crucial roles spanning developmental processes to stress responses. Ca2+ signals are decoded into defined plant adaptive responses by different Ca2+ sensing proteins, including calmodulin (CaM) and calmodulin-like (CML) proteins. Although major advances have been achieved in describing how these Ca2+ decoding proteins interact and regulate downstream target effectors, the molecular details of these processes remain largely unknown. Herein, the kinetics of Ca2+ dissociation from a conserved CaM and two CML isoforms from A. thaliana has been studied by fluorescence stopped-flow spectroscopy. Kinetic data were obtained for the isolated Ca2+-bound proteins as well as for the proteins complexed with different target peptides. Moreover, the lobe specific interactions between the Ca2+ sensing proteins and their targets were characterized by using a panel of protein mutants deficient in Ca2+ binding at the N-lobe or C-lobe. Results were analyzed and discussed in the context of the Ca2+-decoding and Ca2+-controlled target binding mechanisms in plants.
•Ca2+-binding proteins are instrumental in the control of Ca2+ signaling in plants.•The Arabidopsis genome harbours seven calmodulin and 50 calmodulin-like genes.•We measured Ca2+ dissociation rates from AtCaM1, AtCML7 and AtCML19 by rapid kinetics.•CaM and CML proteins show lobe specific Ca2+ dissociation kinetics.•Peptide binding impacts the kinetic properties of Ca2+-binding sites.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34974297</pmid><doi>10.1016/j.bbrc.2021.12.077</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-3902-3512</orcidid><orcidid>https://orcid.org/0000-0002-5921-7365</orcidid><orcidid>https://orcid.org/0000-0002-7341-0970</orcidid></addata></record> |
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subjects | Arabidopsis - drug effects Arabidopsis - metabolism Arabidopsis Proteins - metabolism Arabidopsis thaliana Calcium Calcium - metabolism Calmodulin Calmodulin - metabolism Calmodulin-like proteins Kinetics Melitten - pharmacology Melittin Mutant Proteins - metabolism Peptides - metabolism RAD4 Rapid kinetics SAC3B |
title | Rapid kinetics of calcium dissociation from plant calmodulin and calmodulin-like proteins and effect of target peptides |
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