Orientation of Myosin Binding Protein C in the Cardiac Muscle Sarcomere Determined by Domain-Specific Immuno-EM
Myosin binding protein C is a thick filament protein of vertebrate striated muscle. The cardiac isoform [cardiac myosin binding protein C (cMyBP-C)] is essential for normal cardiac function, and mutations in cMyBP-C cause cardiac muscle disease. The rod-shaped molecule is composed primarily of 11 im...
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description | Myosin binding protein C is a thick filament protein of vertebrate striated muscle. The cardiac isoform [cardiac myosin binding protein C (cMyBP-C)] is essential for normal cardiac function, and mutations in cMyBP-C cause cardiac muscle disease. The rod-shaped molecule is composed primarily of 11 immunoglobulin- or fibronectin-like domains and is located at nine sites, 43nm apart, in each half of the A-band. To understand how cMyBP-C functions, it is important to know its structural organization in the sarcomere, as this will affect its ability to interact with other sarcomeric proteins. Several models, in which cMyBP-C wraps around, extends radially from, or runs axially along the thick filament, have been proposed. Our goal was to define cMyBP-C orientation by determining the relative axial positions of different cMyBP-C domains. Immuno-electron microscopy was performed using mouse cardiac myofibrils labeled with antibodies specific to the N- and C-terminal domains and to the middle of cMyBP-C. Antibodies to all regions of the molecule, except the C-terminus, labeled at the same nine axial positions in each half A-band, consistent with a circumferential and/or radial rather than an axial orientation of the bulk of the molecule. The C-terminal antibody stripes were slightly displaced axially, demonstrating an axial orientation of the C-terminal three domains, with the C-terminus closer to the M-line. These results, combined with previous studies, suggest that the C-terminal domains of cMyBP-C run along the thick filament surface, while the N-terminus extends toward neighboring thin filaments. This organization provides a structural framework for understanding cMyBP-C's modulation of cardiac muscle contraction.
[Display omitted]
•The organization of cMyBP-C in the cardiac muscle sarcomere is controversial.•Cardiac muscle myofibrils were labeled with domain-specific antibodies to cMyBP-C.•The antibodies revealed the axial positions of different domains of cMyBP-C.•Different domains were located at the same axial positions along the thick filament.•We conclude that most of cMyBP-C is oriented perpendicular to the thick filament. |
doi_str_mv | 10.1016/j.jmb.2014.10.023 |
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[Display omitted]
•The organization of cMyBP-C in the cardiac muscle sarcomere is controversial.•Cardiac muscle myofibrils were labeled with domain-specific antibodies to cMyBP-C.•The antibodies revealed the axial positions of different domains of cMyBP-C.•Different domains were located at the same axial positions along the thick filament.•We conclude that most of cMyBP-C is oriented perpendicular to the thick filament.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/j.jmb.2014.10.023</identifier><identifier>PMID: 25451032</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; antibodies ; binding proteins ; cardiac muscle contraction ; cardiac muscle disease ; cardiac muscle regulation ; cardiac muscle structure ; cardiac output ; Carrier Proteins - chemistry ; cMyBP-C ; Image Processing, Computer-Assisted ; Mice ; microscopy ; Microscopy, Fluorescence ; Microscopy, Immunoelectron ; muscle contraction ; mutation ; Myocardial Contraction - physiology ; Myocardium - chemistry ; myosin ; Protein Isoforms - chemistry ; sarcomeres ; Sarcomeres - chemistry ; striated muscle</subject><ispartof>Journal of molecular biology, 2015-01, Vol.427 (2), p.274-286</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><rights>2014 Elsevier Ltd. All rights reserved 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-38a1d30bf2176272d18d5af65c901e59426fd9b9a95caf3dd5a3275dad0d76b13</citedby><cites>FETCH-LOGICAL-c484t-38a1d30bf2176272d18d5af65c901e59426fd9b9a95caf3dd5a3275dad0d76b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022283614005749$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25451032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Kyounghwan</creatorcontrib><creatorcontrib>Harris, Samantha P.</creatorcontrib><creatorcontrib>Sadayappan, Sakthivel</creatorcontrib><creatorcontrib>Craig, Roger</creatorcontrib><title>Orientation of Myosin Binding Protein C in the Cardiac Muscle Sarcomere Determined by Domain-Specific Immuno-EM</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>Myosin binding protein C is a thick filament protein of vertebrate striated muscle. The cardiac isoform [cardiac myosin binding protein C (cMyBP-C)] is essential for normal cardiac function, and mutations in cMyBP-C cause cardiac muscle disease. The rod-shaped molecule is composed primarily of 11 immunoglobulin- or fibronectin-like domains and is located at nine sites, 43nm apart, in each half of the A-band. To understand how cMyBP-C functions, it is important to know its structural organization in the sarcomere, as this will affect its ability to interact with other sarcomeric proteins. Several models, in which cMyBP-C wraps around, extends radially from, or runs axially along the thick filament, have been proposed. Our goal was to define cMyBP-C orientation by determining the relative axial positions of different cMyBP-C domains. Immuno-electron microscopy was performed using mouse cardiac myofibrils labeled with antibodies specific to the N- and C-terminal domains and to the middle of cMyBP-C. Antibodies to all regions of the molecule, except the C-terminus, labeled at the same nine axial positions in each half A-band, consistent with a circumferential and/or radial rather than an axial orientation of the bulk of the molecule. The C-terminal antibody stripes were slightly displaced axially, demonstrating an axial orientation of the C-terminal three domains, with the C-terminus closer to the M-line. These results, combined with previous studies, suggest that the C-terminal domains of cMyBP-C run along the thick filament surface, while the N-terminus extends toward neighboring thin filaments. This organization provides a structural framework for understanding cMyBP-C's modulation of cardiac muscle contraction.
[Display omitted]
•The organization of cMyBP-C in the cardiac muscle sarcomere is controversial.•Cardiac muscle myofibrils were labeled with domain-specific antibodies to cMyBP-C.•The antibodies revealed the axial positions of different domains of cMyBP-C.•Different domains were located at the same axial positions along the thick filament.•We conclude that most of cMyBP-C is oriented perpendicular to the thick filament.</description><subject>Animals</subject><subject>antibodies</subject><subject>binding proteins</subject><subject>cardiac muscle contraction</subject><subject>cardiac muscle disease</subject><subject>cardiac muscle regulation</subject><subject>cardiac muscle structure</subject><subject>cardiac output</subject><subject>Carrier Proteins - chemistry</subject><subject>cMyBP-C</subject><subject>Image Processing, Computer-Assisted</subject><subject>Mice</subject><subject>microscopy</subject><subject>Microscopy, Fluorescence</subject><subject>Microscopy, Immunoelectron</subject><subject>muscle contraction</subject><subject>mutation</subject><subject>Myocardial Contraction - physiology</subject><subject>Myocardium - chemistry</subject><subject>myosin</subject><subject>Protein Isoforms - chemistry</subject><subject>sarcomeres</subject><subject>Sarcomeres - chemistry</subject><subject>striated muscle</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaTZpf0AvRcdevNGHZcsUCu3mE7KkkPYsZGmcaLGkrWQH9t9Xy6ahubSXGUbzzotmHoQ-ULKkhDanm-XG90tGaF3qJWH8FVpQIrtKNly-RgtCGKuY5M0ROs55QwgRvJZv0RETtaCEswWKt8lBmPTkYsBxwOtdzC7gby5YF-7x9xQnKPUKlzA9AF7pZJ02eD1nMwK-08lEDwnwGUyQvAtgcb_DZ9FrF6q7LRg3OIOvvZ9DrM7X79CbQY8Z3j_lE_Tz4vzH6qq6ub28Xn29qUwt66niUlPLST8w2jasZZZKK_TQCNMRCqKrWTPYru90J4weuC1NzlphtSW2bXrKT9CXg-927j1YU3ZMelTb5LxOOxW1Uy87wT2o-_ioata1QjTF4NOTQYq_ZsiT8i4bGEcdIM5ZsXJNWnSt_K-UNoJxSdtuL6UHqUkx5wTD848oUXumaqMKU7Vnun8qTMvMx79XeZ74A7EIPh8EUA766CCpbApUA9YlMJOy0f3D_jd2z7KZ</recordid><startdate>20150130</startdate><enddate>20150130</enddate><creator>Lee, Kyounghwan</creator><creator>Harris, Samantha P.</creator><creator>Sadayappan, Sakthivel</creator><creator>Craig, Roger</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><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20150130</creationdate><title>Orientation of Myosin Binding Protein C in the Cardiac Muscle Sarcomere Determined by Domain-Specific Immuno-EM</title><author>Lee, Kyounghwan ; Harris, Samantha P. ; Sadayappan, Sakthivel ; Craig, Roger</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-38a1d30bf2176272d18d5af65c901e59426fd9b9a95caf3dd5a3275dad0d76b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>antibodies</topic><topic>binding proteins</topic><topic>cardiac muscle contraction</topic><topic>cardiac muscle disease</topic><topic>cardiac muscle regulation</topic><topic>cardiac muscle structure</topic><topic>cardiac output</topic><topic>Carrier Proteins - chemistry</topic><topic>cMyBP-C</topic><topic>Image Processing, Computer-Assisted</topic><topic>Mice</topic><topic>microscopy</topic><topic>Microscopy, Fluorescence</topic><topic>Microscopy, Immunoelectron</topic><topic>muscle contraction</topic><topic>mutation</topic><topic>Myocardial Contraction - physiology</topic><topic>Myocardium - chemistry</topic><topic>myosin</topic><topic>Protein Isoforms - chemistry</topic><topic>sarcomeres</topic><topic>Sarcomeres - chemistry</topic><topic>striated muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Kyounghwan</creatorcontrib><creatorcontrib>Harris, Samantha P.</creatorcontrib><creatorcontrib>Sadayappan, Sakthivel</creatorcontrib><creatorcontrib>Craig, Roger</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><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Kyounghwan</au><au>Harris, Samantha P.</au><au>Sadayappan, Sakthivel</au><au>Craig, Roger</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orientation of Myosin Binding Protein C in the Cardiac Muscle Sarcomere Determined by Domain-Specific Immuno-EM</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2015-01-30</date><risdate>2015</risdate><volume>427</volume><issue>2</issue><spage>274</spage><epage>286</epage><pages>274-286</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>Myosin binding protein C is a thick filament protein of vertebrate striated muscle. The cardiac isoform [cardiac myosin binding protein C (cMyBP-C)] is essential for normal cardiac function, and mutations in cMyBP-C cause cardiac muscle disease. The rod-shaped molecule is composed primarily of 11 immunoglobulin- or fibronectin-like domains and is located at nine sites, 43nm apart, in each half of the A-band. To understand how cMyBP-C functions, it is important to know its structural organization in the sarcomere, as this will affect its ability to interact with other sarcomeric proteins. Several models, in which cMyBP-C wraps around, extends radially from, or runs axially along the thick filament, have been proposed. Our goal was to define cMyBP-C orientation by determining the relative axial positions of different cMyBP-C domains. Immuno-electron microscopy was performed using mouse cardiac myofibrils labeled with antibodies specific to the N- and C-terminal domains and to the middle of cMyBP-C. Antibodies to all regions of the molecule, except the C-terminus, labeled at the same nine axial positions in each half A-band, consistent with a circumferential and/or radial rather than an axial orientation of the bulk of the molecule. The C-terminal antibody stripes were slightly displaced axially, demonstrating an axial orientation of the C-terminal three domains, with the C-terminus closer to the M-line. These results, combined with previous studies, suggest that the C-terminal domains of cMyBP-C run along the thick filament surface, while the N-terminus extends toward neighboring thin filaments. This organization provides a structural framework for understanding cMyBP-C's modulation of cardiac muscle contraction.
[Display omitted]
•The organization of cMyBP-C in the cardiac muscle sarcomere is controversial.•Cardiac muscle myofibrils were labeled with domain-specific antibodies to cMyBP-C.•The antibodies revealed the axial positions of different domains of cMyBP-C.•Different domains were located at the same axial positions along the thick filament.•We conclude that most of cMyBP-C is oriented perpendicular to the thick filament.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25451032</pmid><doi>10.1016/j.jmb.2014.10.023</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals antibodies binding proteins cardiac muscle contraction cardiac muscle disease cardiac muscle regulation cardiac muscle structure cardiac output Carrier Proteins - chemistry cMyBP-C Image Processing, Computer-Assisted Mice microscopy Microscopy, Fluorescence Microscopy, Immunoelectron muscle contraction mutation Myocardial Contraction - physiology Myocardium - chemistry myosin Protein Isoforms - chemistry sarcomeres Sarcomeres - chemistry striated muscle |
title | Orientation of Myosin Binding Protein C in the Cardiac Muscle Sarcomere Determined by Domain-Specific Immuno-EM |
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