{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,21]],"date-time":"2026-05-21T14:50:12Z","timestamp":1779375012313,"version":"3.53.1"},"reference-count":52,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2007,5,4]],"date-time":"2007-05-04T00:00:00Z","timestamp":1178236800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["The Journal of Physiology"],"published-print":{"date-parts":[[2007,5,15]]},"abstract":"<jats:p>\n                    Calsequestrin is a large\u2010capacity Ca\u2010binding protein located in the terminal cisternae of sarcoplasmic reticulum (SR) suggesting a role as a buffer of the concentration of free Ca in the SR ([Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    ) serving to maintain the driving force for SR Ca\n                    <jats:sup>2+<\/jats:sup>\n                    release. Essentially all of the functional studies on calsequestrin to date have been carried out on purified calsequestrin or on disrupted muscle preparations such as terminal cisternae vesicles. To obtain information about calsequestrin's properties during physiological SR Ca\n                    <jats:sup>2+<\/jats:sup>\n                    release, experiments were carried out on frog cut skeletal muscle fibres using two optical methods. One \u2013 the EGTA\u2013phenol red method \u2013 monitored the content of total Ca in the SR ([Ca\n                    <jats:sub>T<\/jats:sub>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    ) and the other used the low affinity Ca indicator tetramethylmurexide (TMX) to monitor the concentration of free Ca in the SR. Both methods relied on a large concentration of the Ca buffer EGTA (20 m\n                    <jats:sc>m<\/jats:sc>\n                    ), in the latter case to greatly reduce the increase in myoplasmic [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ] caused by SR Ca\n                    <jats:sup>2+<\/jats:sup>\n                    release thereby almost eliminating the myoplasmic component of the TMX signal. By releasing almost all of the SR Ca, these optical signals provided information about [Ca\n                    <jats:sub>T<\/jats:sub>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    versus [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    as [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    varied from its resting level ([Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR,R<\/jats:sub>\n                    ) to near zero. Since almost all of the Ca in the SR is bound to calsequestrin, this information closely resembles the binding curve of the Ca\u2013calsequestrin reaction. Calcium binding to calsequestrin was found to be cooperative (estimated Hill coefficient = 2.95) and to have a very high capacity (at the start of Ca\n                    <jats:sup>2+<\/jats:sup>\n                    release, 23 times more Ca was estimated to initiate from calsequestrin as opposed to the pool of free Ca in the SR). The latter result contrasts with an earlier report that only \u223c25% of released Ca\n                    <jats:sup>2+<\/jats:sup>\n                    comes from calsequestrin and \u223c75% comes from the free pool. The value of [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR,R<\/jats:sub>\n                    was close to the\n                    <jats:italic>K<\/jats:italic>\n                    <jats:sub>D<\/jats:sub>\n                    for calsequestrin, which has a value near 1 m\n                    <jats:sc>m<\/jats:sc>\n                    in\n                    <jats:italic>in vitro<\/jats:italic>\n                    studies. Other evidence indicates that [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR,R<\/jats:sub>\n                    is near 1 m\n                    <jats:sc>m<\/jats:sc>\n                    in cut fibres. These results along with the known rapid kinetics of the Ca\u2013calsequestrin binding reaction indicate that calsequestrin's properties are optimized to buffer [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    during rapid, physiological SR Ca\n                    <jats:sup>2+<\/jats:sup>\n                    release. Although the results do not entirely rule out a more active role in the excitation\u2013contraction coupling process, they do indicate that passive buffering of [Ca\n                    <jats:sup>2+<\/jats:sup>\n                    ]\n                    <jats:sub>SR<\/jats:sub>\n                    is a very important function of calsequestrin.\n                  <\/jats:p>","DOI":"10.1113\/jphysiol.2006.126474","type":"journal-article","created":{"date-parts":[[2007,3,1]],"date-time":"2007-03-01T22:56:11Z","timestamp":1172789771000},"page":"319-367","source":"Crossref","is-referenced-by-count":31,"title":["Role of calsequestrin evaluated from changes in free and total calcium concentrations in the sarcoplasmic reticulum of frog cut skeletal muscle fibres"],"prefix":"10.1113","volume":"581","author":[{"given":"Paul C.","family":"Pape","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karine","family":"F\u00e9nelon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C\u00e9dric R. 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