Some Perspectives on the Viscosity of Actin Filaments
Measurements of the dynamic viscosity of various actin filament preparations under conditions of low and controlled shear: (a) confirm the shear rate dependence of F-actin viscosities and show that this dependence obeys the power law relationship observed for entangled synthetic polymers; (b) permit...
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Veröffentlicht in: | The Journal of cell biology 1982-06, Vol.93 (3), p.987-991 |
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description | Measurements of the dynamic viscosity of various actin filament preparations under conditions of low and controlled shear: (a) confirm the shear rate dependence of F-actin viscosities and show that this dependence obeys the power law relationship observed for entangled synthetic polymers; (b) permit estimation of the extent to which shear artifact amplifies changes in the apparent viscosity of F-actin measured in a falling ball viscometer; (c) show that gel-filtration chromatography of actin and the addition of cytochalasin B to F-actin bring about small (20-40%) changes in the viscosity of the F-actin solutions. These variations are consistent with alterations in the actin-binding protein concentrations required for incipient gelation, a parameter inversely related to average filament length. Therefore: (a) changes in the viscosity of F-actin can be magnified by use of the falling ball viscometer, and may exaggerate their biological importance; (b) chromatography of actin may not be required to obtain meaningful information about the rheology of actin filaments; (c) changes in actin filament length can satisfactorily explain alterations in F-actin viscosity exerted by cytochalasin B and by chromatography, obviating the need to postulate specific interfilament interactions. |
doi_str_mv | 10.1083/jcb.93.3.987 |
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These variations are consistent with alterations in the actin-binding protein concentrations required for incipient gelation, a parameter inversely related to average filament length. Therefore: (a) changes in the viscosity of F-actin can be magnified by use of the falling ball viscometer, and may exaggerate their biological importance; (b) chromatography of actin may not be required to obtain meaningful information about the rheology of actin filaments; (c) changes in actin filament length can satisfactorily explain alterations in F-actin viscosity exerted by cytochalasin B and by chromatography, obviating the need to postulate specific interfilament interactions.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.93.3.987</identifier><identifier>PMID: 6889602</identifier><language>eng</language><publisher>United States: Rockefeller University Press</publisher><subject>Actins ; Actins - metabolism ; Carrier Proteins - metabolism ; Chromatography ; Cytochalasin B - pharmacology ; Cytochalasins ; Cytoskeleton ; Gelsolin ; Microfilament Proteins ; Microfilaments ; Polymerization ; Polymers ; Rapid Communications ; Rheology ; Viscometers ; Viscosity</subject><ispartof>The Journal of cell biology, 1982-06, Vol.93 (3), p.987-991</ispartof><rights>Copyright 1982 The Rockefeller University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-f0295d5055d9e83e95e8027055538631d3d7bb7c4dbf2eda5c505972e878cffc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6889602$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zaner, Ken S.</creatorcontrib><creatorcontrib>Stossel, Thomas P.</creatorcontrib><title>Some Perspectives on the Viscosity of Actin Filaments</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Measurements of the dynamic viscosity of various actin filament preparations under conditions of low and controlled shear: (a) confirm the shear rate dependence of F-actin viscosities and show that this dependence obeys the power law relationship observed for entangled synthetic polymers; (b) permit estimation of the extent to which shear artifact amplifies changes in the apparent viscosity of F-actin measured in a falling ball viscometer; (c) show that gel-filtration chromatography of actin and the addition of cytochalasin B to F-actin bring about small (20-40%) changes in the viscosity of the F-actin solutions. These variations are consistent with alterations in the actin-binding protein concentrations required for incipient gelation, a parameter inversely related to average filament length. Therefore: (a) changes in the viscosity of F-actin can be magnified by use of the falling ball viscometer, and may exaggerate their biological importance; (b) chromatography of actin may not be required to obtain meaningful information about the rheology of actin filaments; (c) changes in actin filament length can satisfactorily explain alterations in F-actin viscosity exerted by cytochalasin B and by chromatography, obviating the need to postulate specific interfilament interactions.</description><subject>Actins</subject><subject>Actins - metabolism</subject><subject>Carrier Proteins - metabolism</subject><subject>Chromatography</subject><subject>Cytochalasin B - pharmacology</subject><subject>Cytochalasins</subject><subject>Cytoskeleton</subject><subject>Gelsolin</subject><subject>Microfilament Proteins</subject><subject>Microfilaments</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Rapid Communications</subject><subject>Rheology</subject><subject>Viscometers</subject><subject>Viscosity</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkM1Lw0AQxRdRaq3ePCrk5MnE2d1ssnsRSrEqFBT8uC7JZmJTkmzNpoX-925pqXoahvfjvZlHyCWFiILkdwuTR4pHPFIyPSJDKmIIJY3hmAwBGA2VYOKUnDm3AIA4jfmADBIpVQJsSMSbbTB4xc4t0fTVGl1g26CfY_BZOWNd1W8CWwZjr7XBtKqzBtvenZOTMqsdXuzniHxMH94nT-Hs5fF5Mp6FJgbowxKYEoUAIQqFkqMSKIGlfhdcJpwWvEjzPDVxkZcMi0wYz6qUoUylKUvDR-R-57tc5Q0Wxmd3Wa2XXdVk3UbbrNL_lbaa6y-71oxSRhn3Bjd7g85-r9D1uvFvYV1nLdqV02lMlWLxFrzdgaazznVYHkIo6G3N2tesFddc-5o9fv33sAO879XrVzt94Xrb_XoloJRP-wHf6YJX</recordid><startdate>19820601</startdate><enddate>19820601</enddate><creator>Zaner, Ken S.</creator><creator>Stossel, Thomas P.</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>5PM</scope></search><sort><creationdate>19820601</creationdate><title>Some Perspectives on the Viscosity of Actin Filaments</title><author>Zaner, Ken S. ; Stossel, Thomas P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-f0295d5055d9e83e95e8027055538631d3d7bb7c4dbf2eda5c505972e878cffc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Actins</topic><topic>Actins - metabolism</topic><topic>Carrier Proteins - metabolism</topic><topic>Chromatography</topic><topic>Cytochalasin B - pharmacology</topic><topic>Cytochalasins</topic><topic>Cytoskeleton</topic><topic>Gelsolin</topic><topic>Microfilament Proteins</topic><topic>Microfilaments</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Rapid Communications</topic><topic>Rheology</topic><topic>Viscometers</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaner, Ken S.</creatorcontrib><creatorcontrib>Stossel, Thomas P.</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaner, Ken S.</au><au>Stossel, Thomas P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Some Perspectives on the Viscosity of Actin Filaments</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>1982-06-01</date><risdate>1982</risdate><volume>93</volume><issue>3</issue><spage>987</spage><epage>991</epage><pages>987-991</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><abstract>Measurements of the dynamic viscosity of various actin filament preparations under conditions of low and controlled shear: (a) confirm the shear rate dependence of F-actin viscosities and show that this dependence obeys the power law relationship observed for entangled synthetic polymers; (b) permit estimation of the extent to which shear artifact amplifies changes in the apparent viscosity of F-actin measured in a falling ball viscometer; (c) show that gel-filtration chromatography of actin and the addition of cytochalasin B to F-actin bring about small (20-40%) changes in the viscosity of the F-actin solutions. These variations are consistent with alterations in the actin-binding protein concentrations required for incipient gelation, a parameter inversely related to average filament length. Therefore: (a) changes in the viscosity of F-actin can be magnified by use of the falling ball viscometer, and may exaggerate their biological importance; (b) chromatography of actin may not be required to obtain meaningful information about the rheology of actin filaments; (c) changes in actin filament length can satisfactorily explain alterations in F-actin viscosity exerted by cytochalasin B and by chromatography, obviating the need to postulate specific interfilament interactions.</abstract><cop>United States</cop><pub>Rockefeller University Press</pub><pmid>6889602</pmid><doi>10.1083/jcb.93.3.987</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Actins Actins - metabolism Carrier Proteins - metabolism Chromatography Cytochalasin B - pharmacology Cytochalasins Cytoskeleton Gelsolin Microfilament Proteins Microfilaments Polymerization Polymers Rapid Communications Rheology Viscometers Viscosity |
title | Some Perspectives on the Viscosity of Actin Filaments |
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