Smooth muscle tropomyosin coiled-coil dimers. Subunit composition, assembly, and end-to-end interaction
- PMID: 2005125
Smooth muscle tropomyosin coiled-coil dimers. Subunit composition, assembly, and end-to-end interaction
Abstract
Subunits of gizzard smooth muscle tropomyosin, dissociated by guanidinium chloride and reassociated by high salt dialysis, form a 1:1 mixture of the beta beta and gamma gamma homodimers (Graceffa, P. (1989) Biochemistry 28, 1282-1287). The homodimers have now been separated by anion-exchange chromatography and native gel electrophoresis, enabling us to show that the native protein is composed of more than 90% heterodimer. The in vitro equilibrium distribution of heterodimer and homodimers, at close to physiological temperature and ionic conditions, was calculated from thermal unfolding profiles of separated homodimers and heterodimer, as monitored by circular dichroism. The results, for an equal proportion of beta and gamma chains, indicate a predominant formation of heterodimer via chain dissociation and chain exchange, although the proportion of heterodimer was much less than the 90-100% found in the native protein. However, the proportion of heterodimer for actin-bound tropomyosin, determined by analyzing tropomyosin sedimented with actin, was greater than 90%, which may provide a model for assembly in vivo. The end-to-end interactions of the homodimers are about the same but are much less than that of the native heterodimer, as determined by viscometry. The greater end-to-end interaction of heterodimers may lead to stronger binding to actin compared to homodimers and thus would further shift the equilibrium between heterodimer and homodimers toward heterodimer and possibly account for the almost exclusive population of heterodimer in the presence of actin. The greater end-to-end interaction of the heterodimer may also provide a functional advantage for its preferred assembly. This study also shows that the two-step thermal unfolding of the homodimer mixture is due to the formation of heterodimer via an intermediate which is a new type of tropomyosin species which forms a gel in low salt. This tropomyosin is also present in small amounts in native tropomyosin preparations.
Similar articles
-
Unfolding/refolding studies of smooth muscle tropomyosin. Evidence for a chain exchange mechanism in the preferential assembly of the native heterodimer.J Biol Chem. 1990 Jan 15;265(2):1134-8. J Biol Chem. 1990. PMID: 2295604
-
In-register homodimers of smooth muscle tropomyosin.Biochemistry. 1989 Feb 7;28(3):1282-7. doi: 10.1021/bi00429a050. Biochemistry. 1989. PMID: 2713364
-
Heat-treated smooth muscle tropomyosin.Biochim Biophys Acta. 1992 Apr 8;1120(2):205-7. doi: 10.1016/0167-4838(92)90271-e. Biochim Biophys Acta. 1992. PMID: 1562588
-
Dimerization of tropomyosins.Adv Exp Med Biol. 2008;644:73-84. doi: 10.1007/978-0-387-85766-4_6. Adv Exp Med Biol. 2008. PMID: 19209814 Review.
-
Role of tropomyosin in the regulation of contraction in smooth muscle.Adv Exp Med Biol. 2008;644:110-23. doi: 10.1007/978-0-387-85766-4_9. Adv Exp Med Biol. 2008. PMID: 19209817 Review.
Cited by
-
α-Tropomyosin with a D175N or E180G mutation in only one chain differs from tropomyosin with mutations in both chains.Biochemistry. 2012 Dec 11;51(49):9880-90. doi: 10.1021/bi301323n. Epub 2012 Nov 30. Biochemistry. 2012. PMID: 23170982 Free PMC article.
-
In vitro formation and characterization of the skeletal muscle α·β tropomyosin heterodimers.Biochemistry. 2012 Aug 14;51(32):6388-99. doi: 10.1021/bi300340r. Epub 2012 Aug 3. Biochemistry. 2012. PMID: 22812662 Free PMC article.
-
Acrylodan-labeled smooth muscle tropomyosin reports differences in the effects of troponin and caldesmon in the transition from the active state to the inactive state.Biochemistry. 2011 Jul 12;50(27):6093-101. doi: 10.1021/bi200288c. Epub 2011 Jun 14. Biochemistry. 2011. PMID: 21639115 Free PMC article.
-
Opposing roles of the extracellular signal-regulated kinase and p38 mitogen-activated protein kinase cascades in Ras-mediated downregulation of tropomyosin.Mol Cell Biol. 2002 Apr;22(7):2304-17. doi: 10.1128/MCB.22.7.2304-2317.2002. Mol Cell Biol. 2002. PMID: 11884615 Free PMC article.
-
Groundnut bud necrosis virus encoded NSm associates with membranes via its C-terminal domain.PLoS One. 2014 Jun 11;9(6):e99370. doi: 10.1371/journal.pone.0099370. eCollection 2014. PLoS One. 2014. PMID: 24919116 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources