To lie or not to lie: Super-relaxing with myosins
Since the discovery of muscle in the 19th century, myosins as molecular motors have been extensively studied. However, in the last decade, a new functional super-relaxed (SRX) state of myosin has been discovered, which has a 10-fold slower ATP turnover rate than the already-known non-actin-bound, di...
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description | Since the discovery of muscle in the 19th century, myosins as molecular motors have been extensively studied. However, in the last decade, a new functional super-relaxed (SRX) state of myosin has been discovered, which has a 10-fold slower ATP turnover rate than the already-known non-actin-bound, disordered relaxed (DRX) state. These two states are in dynamic equilibrium under resting muscle conditions and are thought to be significant contributors to adaptive thermogenesis in skeletal muscle and can act as a reserve pool that may be recruited when there is a sustained demand for increased cardiac muscle power. This report provides an evolutionary perspective of how striated muscle contraction is regulated by modulating this myosin DRX SRX state equilibrium. We further discuss this equilibrium with respect to different physiological and pathophysiological perturbations, including insults causing hypertrophic cardiomyopathy, and small-molecule effectors that modulate muscle contractility in diseased pathology. |
doi_str_mv | 10.7554/eLife.63703 |
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We further discuss this equilibrium with respect to different physiological and pathophysiological perturbations, including insults causing hypertrophic cardiomyopathy, and small-molecule effectors that modulate muscle contractility in diseased pathology.</description><identifier>ISSN: 2050-084X</identifier><identifier>EISSN: 2050-084X</identifier><identifier>DOI: 10.7554/eLife.63703</identifier><identifier>PMID: 33565963</identifier><language>eng</language><publisher>CAMBRIDGE: Elife Sciences Publications Ltd</publisher><subject>Actin ; Animals ; Binding sites ; Biochemistry and Chemical Biology ; Biology ; Cardiac muscle ; Cardiomyopathy ; Cell division ; Enzymes ; Equilibrium ; Humans ; Hypertrophic cardiomyopathy ; Interacting heads motif ; Life Sciences & Biomedicine ; Life Sciences & Biomedicine - Other Topics ; Mavacamten ; Muscle Contraction ; Muscle proteins ; Muscle, Skeletal - physiology ; Muscles ; Myosin ; Myosins - physiology ; Phosphorylation ; Physiological aspects ; Physiology ; Review ; Science & Technology ; Skeletal muscle ; Smooth muscle ; Structural Biology and Molecular Biophysics ; Super-relaxed state ; Thermogenesis</subject><ispartof>eLife, 2021-02, Vol.10, Article 63703</ispartof><rights>2021, Nag and Trivedi.</rights><rights>COPYRIGHT 2021 eLife Science Publications, Ltd.</rights><rights>2021, Nag and Trivedi. 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However, in the last decade, a new functional super-relaxed (SRX) state of myosin has been discovered, which has a 10-fold slower ATP turnover rate than the already-known non-actin-bound, disordered relaxed (DRX) state. These two states are in dynamic equilibrium under resting muscle conditions and are thought to be significant contributors to adaptive thermogenesis in skeletal muscle and can act as a reserve pool that may be recruited when there is a sustained demand for increased cardiac muscle power. This report provides an evolutionary perspective of how striated muscle contraction is regulated by modulating this myosin DRX <-> SRX state equilibrium. We further discuss this equilibrium with respect to different physiological and pathophysiological perturbations, including insults causing hypertrophic cardiomyopathy, and small-molecule effectors that modulate muscle contractility in diseased pathology.</description><subject>Actin</subject><subject>Animals</subject><subject>Binding sites</subject><subject>Biochemistry and Chemical Biology</subject><subject>Biology</subject><subject>Cardiac muscle</subject><subject>Cardiomyopathy</subject><subject>Cell division</subject><subject>Enzymes</subject><subject>Equilibrium</subject><subject>Humans</subject><subject>Hypertrophic cardiomyopathy</subject><subject>Interacting heads motif</subject><subject>Life Sciences & Biomedicine</subject><subject>Life Sciences & Biomedicine - Other Topics</subject><subject>Mavacamten</subject><subject>Muscle Contraction</subject><subject>Muscle proteins</subject><subject>Muscle, Skeletal - physiology</subject><subject>Muscles</subject><subject>Myosin</subject><subject>Myosins - physiology</subject><subject>Phosphorylation</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>Review</subject><subject>Science & Technology</subject><subject>Skeletal muscle</subject><subject>Smooth muscle</subject><subject>Structural Biology and Molecular Biophysics</subject><subject>Super-relaxed state</subject><subject>Thermogenesis</subject><issn>2050-084X</issn><issn>2050-084X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkktvEzEUhUcIRKvSFXs0EhsQSrDHz2GBVEU8IkVColmws2zPndTRxC62h7b_HicpaYNYYC_8-u6xfXSq6iVGU8EYfQ8L18OUE4HIk-q0QQxNkKQ_nj6an1TnKa1RaYJKidvn1QkhjLOWk9MKL0M9OKhDrH3Idd6tPtSX4zXESYRB3zq_qm9cvqo3dyE5n15Uz3o9JDi_H8-q5edPy9nXyeLbl_nsYjGxTPA8oQgxhnUPQA3TEmTXma4hwnBMNBBi-o4b3FDKCLaGA9GiFT2VvBG9IZacVfO9bBf0Wl1Ht9HxTgXt1G4jxJXSMTs7gOo4aE01QeV3tLNt24Pg1BjJCDOSs6L1ca91PZoNdBZ8jno4Ej0-8e5KrcIvJWQxmZMi8OZeIIafI6SsNi5ZGAbtIYxJNTtjW4q2d73-C12HMfrilGpYy7BEiPMHaqXLB5zvQ7nXbkXVBWeYCCxwU6jpP6jSO9g4Gzz0ruwfFbw9KihMhtu80mNKan75_Zh9t2dtDClF6A9-YKS22VK7bKldtgr96rGFB_ZPkgog98ANmNAn68BbOGAlfBy3vJHtNod45rLOLvhZGH1-eMn_lJLf-HbnHg</recordid><startdate>20210210</startdate><enddate>20210210</enddate><creator>Nag, Suman</creator><creator>Trivedi, Darshan</creator><general>Elife Sciences Publications Ltd</general><general>eLife Science Publications, Ltd</general><general>eLife Sciences Publications Ltd</general><general>eLife Sciences Publications, Ltd</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><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>ISR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1817-8275</orcidid><orcidid>https://orcid.org/0000-0002-4188-3570</orcidid></search><sort><creationdate>20210210</creationdate><title>To lie or not to lie: Super-relaxing with myosins</title><author>Nag, Suman ; 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However, in the last decade, a new functional super-relaxed (SRX) state of myosin has been discovered, which has a 10-fold slower ATP turnover rate than the already-known non-actin-bound, disordered relaxed (DRX) state. These two states are in dynamic equilibrium under resting muscle conditions and are thought to be significant contributors to adaptive thermogenesis in skeletal muscle and can act as a reserve pool that may be recruited when there is a sustained demand for increased cardiac muscle power. This report provides an evolutionary perspective of how striated muscle contraction is regulated by modulating this myosin DRX <-> SRX state equilibrium. We further discuss this equilibrium with respect to different physiological and pathophysiological perturbations, including insults causing hypertrophic cardiomyopathy, and small-molecule effectors that modulate muscle contractility in diseased pathology.</abstract><cop>CAMBRIDGE</cop><pub>Elife Sciences Publications Ltd</pub><pmid>33565963</pmid><doi>10.7554/eLife.63703</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-1817-8275</orcidid><orcidid>https://orcid.org/0000-0002-4188-3570</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Actin Animals Binding sites Biochemistry and Chemical Biology Biology Cardiac muscle Cardiomyopathy Cell division Enzymes Equilibrium Humans Hypertrophic cardiomyopathy Interacting heads motif Life Sciences & Biomedicine Life Sciences & Biomedicine - Other Topics Mavacamten Muscle Contraction Muscle proteins Muscle, Skeletal - physiology Muscles Myosin Myosins - physiology Phosphorylation Physiological aspects Physiology Review Science & Technology Skeletal muscle Smooth muscle Structural Biology and Molecular Biophysics Super-relaxed state Thermogenesis |
title | To lie or not to lie: Super-relaxing with myosins |
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