Importance of Potential Interhelical Salt-bridges Involving Interior Residues for Coiled-coil Stability and Quaternary Structure
Coiled coils are formed by two or more α-helices that align in a parallel or an antiparallel relative orientation. Polar interactions involving residues at the interior a and d positions are important for determining the quaternary structure of coiled coils. In the model heterodimeric coiled-coil Ac...
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Veröffentlicht in: | Journal of molecular biology 2002-11, Vol.324 (2), p.257-270 |
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creator | McClain, Diana L Gurnon, Daniel G Oakley, Martha G |
description | Coiled coils are formed by two or more α-helices that align in a parallel or an antiparallel relative orientation. Polar interactions involving residues at the interior
a and
d positions are important for determining the quaternary structure of coiled coils. In the model heterodimeric coiled-coil Acid-a1-Base-a1, a buried
a–
d′ Asn–Asn interaction is sufficient to specify both a dimeric structure and an antiparallel relative helix orientation. Although the equivalent
a–
a′ interaction is found in parallel coiled coils, there is no example of an
a–
d′ Asn–Asn interaction in structurally characterized, naturally occurring antiparallel coiled coils. Instead, interior charged residues form interhelical salt-bridges with residues at the adjacent
e or
g positions. Using a model coiled-coil heterodimer, we have explored the role of a potential interhelical interaction between an Arg at an interior
d position and a Glu at the adjacent
g′ position. Our results demonstrate that this potentially attractive interhelical Coulombic interaction has little or no influence on helix orientation. Instead, we show that burying a single Arg residue at an interior position is sufficient to specify a dimeric state at a significantly lower thermodynamic cost than burial of two interacting Asn residues. |
doi_str_mv | 10.1016/S0022-2836(02)01072-0 |
format | Article |
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a and
d positions are important for determining the quaternary structure of coiled coils. In the model heterodimeric coiled-coil Acid-a1-Base-a1, a buried
a–
d′ Asn–Asn interaction is sufficient to specify both a dimeric structure and an antiparallel relative helix orientation. Although the equivalent
a–
a′ interaction is found in parallel coiled coils, there is no example of an
a–
d′ Asn–Asn interaction in structurally characterized, naturally occurring antiparallel coiled coils. Instead, interior charged residues form interhelical salt-bridges with residues at the adjacent
e or
g positions. Using a model coiled-coil heterodimer, we have explored the role of a potential interhelical interaction between an Arg at an interior
d position and a Glu at the adjacent
g′ position. Our results demonstrate that this potentially attractive interhelical Coulombic interaction has little or no influence on helix orientation. Instead, we show that burying a single Arg residue at an interior position is sufficient to specify a dimeric state at a significantly lower thermodynamic cost than burial of two interacting Asn residues.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/S0022-2836(02)01072-0</identifier><identifier>PMID: 12441105</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Amino Acid Sequence ; buried polar interactions ; Circular Dichroism ; coiled coil ; Dimerization ; helix orientation specificity ; Hydrogen Bonding ; Models, Molecular ; Molecular Sequence Data ; oligomerization state ; Peptides - chemistry ; Peptides - metabolism ; Protein Binding ; Protein Folding ; Protein Structure, Quaternary ; Protein Structure, Secondary ; protein–protein interactions ; Sequence Homology, Amino Acid ; Sodium Chloride - chemistry ; Sodium Chloride - metabolism ; Static Electricity ; Substrate Specificity ; Sulfhydryl Compounds - metabolism ; Temperature ; Thermodynamics</subject><ispartof>Journal of molecular biology, 2002-11, Vol.324 (2), p.257-270</ispartof><rights>2002 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-58e48200bb5b4ea95c8b5b32a26b598cd31e27f7bacaecdecd8cda176a98cbcf3</citedby><cites>FETCH-LOGICAL-c361t-58e48200bb5b4ea95c8b5b32a26b598cd31e27f7bacaecdecd8cda176a98cbcf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-2836(02)01072-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12441105$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McClain, Diana L</creatorcontrib><creatorcontrib>Gurnon, Daniel G</creatorcontrib><creatorcontrib>Oakley, Martha G</creatorcontrib><title>Importance of Potential Interhelical Salt-bridges Involving Interior Residues for Coiled-coil Stability and Quaternary Structure</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>Coiled coils are formed by two or more α-helices that align in a parallel or an antiparallel relative orientation. Polar interactions involving residues at the interior
a and
d positions are important for determining the quaternary structure of coiled coils. In the model heterodimeric coiled-coil Acid-a1-Base-a1, a buried
a–
d′ Asn–Asn interaction is sufficient to specify both a dimeric structure and an antiparallel relative helix orientation. Although the equivalent
a–
a′ interaction is found in parallel coiled coils, there is no example of an
a–
d′ Asn–Asn interaction in structurally characterized, naturally occurring antiparallel coiled coils. Instead, interior charged residues form interhelical salt-bridges with residues at the adjacent
e or
g positions. Using a model coiled-coil heterodimer, we have explored the role of a potential interhelical interaction between an Arg at an interior
d position and a Glu at the adjacent
g′ position. Our results demonstrate that this potentially attractive interhelical Coulombic interaction has little or no influence on helix orientation. Instead, we show that burying a single Arg residue at an interior position is sufficient to specify a dimeric state at a significantly lower thermodynamic cost than burial of two interacting Asn residues.</description><subject>Amino Acid Sequence</subject><subject>buried polar interactions</subject><subject>Circular Dichroism</subject><subject>coiled coil</subject><subject>Dimerization</subject><subject>helix orientation specificity</subject><subject>Hydrogen Bonding</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>oligomerization state</subject><subject>Peptides - chemistry</subject><subject>Peptides - metabolism</subject><subject>Protein Binding</subject><subject>Protein Folding</subject><subject>Protein Structure, Quaternary</subject><subject>Protein Structure, Secondary</subject><subject>protein–protein interactions</subject><subject>Sequence Homology, Amino Acid</subject><subject>Sodium Chloride - chemistry</subject><subject>Sodium Chloride - metabolism</subject><subject>Static Electricity</subject><subject>Substrate Specificity</subject><subject>Sulfhydryl Compounds - metabolism</subject><subject>Temperature</subject><subject>Thermodynamics</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1vEzEQhi0EoqHlJ4D2hOCwZez9ck4IRdBGqkQh5Wz5Y7YYOetgeyP11p_OtIngWMnSePy-8-GHsTcczjnw_uMGQIhayKZ_D-IDcBhEDc_YgoNc1rJv5HO2-Gc5Ya9y_g0AXdPKl-yEi7blHLoFu19vdzEVPVms4lhdx4JT8TpU66lg-oXBW0o2OpTaJO9uMZOyj2Hvp9uDx8dU_cDs3UzaSMkq-oCuthSqTdHGB1_uKj256vusqWDS6Y6ENNsyJzxjL0YdMr4-xlP28-uXm9VlffXtYr36fFXbpuel7iS2UgAY05kW9bKzkm6N0KI33VJa13AUwzgYbTVaR4feNB96TaKxY3PK3h367lL8Q6sWtfXZYgh6wjhnNYgBuICBjN3BaFPMOeGodslvaWfFQT2gV4_o1QNXBUI9oldAdW-PA2azRfe_6siaDJ8OBqRv7j0mla1HAu98QluUi_6JEX8BcSyXHg</recordid><startdate>20021122</startdate><enddate>20021122</enddate><creator>McClain, Diana L</creator><creator>Gurnon, Daniel G</creator><creator>Oakley, Martha G</creator><general>Elsevier Ltd</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></search><sort><creationdate>20021122</creationdate><title>Importance of Potential Interhelical Salt-bridges Involving Interior Residues for Coiled-coil Stability and Quaternary Structure</title><author>McClain, Diana L ; Gurnon, Daniel G ; Oakley, Martha G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-58e48200bb5b4ea95c8b5b32a26b598cd31e27f7bacaecdecd8cda176a98cbcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Sequence</topic><topic>buried polar interactions</topic><topic>Circular Dichroism</topic><topic>coiled coil</topic><topic>Dimerization</topic><topic>helix orientation specificity</topic><topic>Hydrogen Bonding</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>oligomerization state</topic><topic>Peptides - chemistry</topic><topic>Peptides - metabolism</topic><topic>Protein Binding</topic><topic>Protein Folding</topic><topic>Protein Structure, Quaternary</topic><topic>Protein Structure, Secondary</topic><topic>protein–protein interactions</topic><topic>Sequence Homology, Amino Acid</topic><topic>Sodium Chloride - chemistry</topic><topic>Sodium Chloride - metabolism</topic><topic>Static Electricity</topic><topic>Substrate Specificity</topic><topic>Sulfhydryl Compounds - metabolism</topic><topic>Temperature</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McClain, Diana L</creatorcontrib><creatorcontrib>Gurnon, Daniel G</creatorcontrib><creatorcontrib>Oakley, Martha G</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>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McClain, Diana L</au><au>Gurnon, Daniel G</au><au>Oakley, Martha G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Importance of Potential Interhelical Salt-bridges Involving Interior Residues for Coiled-coil Stability and Quaternary Structure</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2002-11-22</date><risdate>2002</risdate><volume>324</volume><issue>2</issue><spage>257</spage><epage>270</epage><pages>257-270</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>Coiled coils are formed by two or more α-helices that align in a parallel or an antiparallel relative orientation. Polar interactions involving residues at the interior
a and
d positions are important for determining the quaternary structure of coiled coils. In the model heterodimeric coiled-coil Acid-a1-Base-a1, a buried
a–
d′ Asn–Asn interaction is sufficient to specify both a dimeric structure and an antiparallel relative helix orientation. Although the equivalent
a–
a′ interaction is found in parallel coiled coils, there is no example of an
a–
d′ Asn–Asn interaction in structurally characterized, naturally occurring antiparallel coiled coils. Instead, interior charged residues form interhelical salt-bridges with residues at the adjacent
e or
g positions. Using a model coiled-coil heterodimer, we have explored the role of a potential interhelical interaction between an Arg at an interior
d position and a Glu at the adjacent
g′ position. Our results demonstrate that this potentially attractive interhelical Coulombic interaction has little or no influence on helix orientation. Instead, we show that burying a single Arg residue at an interior position is sufficient to specify a dimeric state at a significantly lower thermodynamic cost than burial of two interacting Asn residues.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>12441105</pmid><doi>10.1016/S0022-2836(02)01072-0</doi><tpages>14</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE |
subjects | Amino Acid Sequence buried polar interactions Circular Dichroism coiled coil Dimerization helix orientation specificity Hydrogen Bonding Models, Molecular Molecular Sequence Data oligomerization state Peptides - chemistry Peptides - metabolism Protein Binding Protein Folding Protein Structure, Quaternary Protein Structure, Secondary protein–protein interactions Sequence Homology, Amino Acid Sodium Chloride - chemistry Sodium Chloride - metabolism Static Electricity Substrate Specificity Sulfhydryl Compounds - metabolism Temperature Thermodynamics |
title | Importance of Potential Interhelical Salt-bridges Involving Interior Residues for Coiled-coil Stability and Quaternary Structure |
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