Home LiteratureArticle Details
PMID: 2263608 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The low-affinity Ca2(+)-binding sites in cardiac/slow skeletal muscle troponin C perform distinct functions: site I alone cannot trigger contraction.

Sweeney HL, Brito RM, Rosevear PR, Putkey JA

Abstract

Both troponin C (TnC) and calmodulin share a remarkably similar tertiary motif that may be common to other Ca2(+)-binding proteins with activator activity. TnC plays a critical role in regulating muscle contraction and is particularly well-suited for structural analysis by site-directed mutation. Fast-twitch skeletal muscle TnC has two low-affinity Ca2(+)-binding sites (sites I and II), while in cardiac and slow-twitch skeletal muscle TnC site I is inactive. Recently, using protein engineering, we directly demonstrated that binding of Ca2+ to the low-affinity site(s) initiates muscle contraction. In the present study, we use mutagenesis to determine whether either of the low-affinity sites in cardiac TnC can trigger contraction in slow-twitch skeletal muscle fibers. In one Ca2(+)-binding mutant, Ca2(+)-binding to the dormant low-affinity site I was restored (CBM+I). In a second mutant, site I was activated while site II was inactivated (CBM+I-IIA). Both proteins had the predicted CA2(+)-binding characteristics, and both were able to associate with troponin I and troponin T to form a troponin complex and integrate into permeabilized slow-twitch skeletal muscle fibers. A comparison of NMR spectra shows the aromatic regions in the two proteins to be qualitatively similar without divalent cations but markedly different with Ca2+. Mutant CBM+I supported force generation in skinned slow skeletal muscle fibers but had Sr2+ and Ca2+ sensitivities similar to fast skeletal TnC. Mutant CBM+I-IIA was unable to restore Ca2(+)-dependent contraction to TnC-depleted skinned slow muscle fibers. The data directly demonstrate that low-affinity sites I and II have distinct functions and that only site II in cardiac TnC can trigger muscle contraction in slow-twitch skeletal muscle fibers. This principle of distinct, modular activities for Ca2(+)-binding sites in the same protein may apply to other members of the TnC/calmodulin family.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Calcium/metabolism Calcium Chloride/metabolism Heart/physiology Kinetics Magnetic Resonance Spectroscopy Molecular Sequence Data Muscle Contraction Muscles/physiology Mutagenesis, Site-Directed Myocardial Contraction Troponin/genetics,metabolism,physiology Troponin C
Chemicals
Troponin Troponin C Calcium Chloride Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sweeney H L
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085.
Brito R M
Rosevear P R
Putkey J A
References (28)
28 references, click to expand
  1. Functional significance of the central helix in calmodulin.
    J Biol Chem. 1988 Aug 15;263(23):11242-9 PMID: 2841323
  2. Cloning, expression, and site-directed mutagenesis of chicken skeletal muscle troponin C.
    J Biol Chem. 1988 Feb 15;263(5):2371-6 PMID: 2963002
  3. Synthesis of a troponin C cDNA and expression of wild-type and mutant proteins in Escherichia coli.
    J Biol Chem. 1988 Sep 25;263(27):13962-9 PMID: 2971047
  4. Skinned ventricular fibres: troponin C extraction is species-dependent and its replacement with skeletal troponin C changes Sr2+ activation properties.
    J Muscle Res Cell Motil. 1988 Apr;9(2):165-73 PMID: 3417854
  5. Effect of substitution of troponin C in cardiac myofibrils with skeletal troponin C or calmodulin on the Ca2+- and Sr2+-sensitive ATPase activity.
    J Biochem. 1988 Jul;104(1):149-54 PMID: 2975654
  6. Site-directed mutation of the trigger calcium-binding sites in cardiac troponin C.
    J Biol Chem. 1989 Jul 25;264(21):12370-8 PMID: 2745448
  7. Time-resolved fluorescence study of VU-9 calmodulin, an engineered calmodulin possessing a single tryptophan residue.
    Biochemistry. 1989 Jul 11;28(14):6093-8 PMID: 2775754
  8. The EF-hand family of calcium-modulated proteins.
    Trends Neurosci. 1989 Nov;12(11):462-7 PMID: 2479149
  9. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  10. Carp muscle calcium-binding protein. II. Structure determination and general description.
    J Biol Chem. 1973 May 10;248(9):3313-26 PMID: 4700463
  11. The calcium and magnesium binding sites on troponin and their role in the regulation of myofibrillar adenosine triphosphatase.
    J Biol Chem. 1975 Jun 25;250(12):4628-33 PMID: 124731
  12. The amino acid sequence of bovine cardiac tamponin-C. Comparison with rabbit skeletal troponin-C.
    Biochem Biophys Res Commun. 1975 May 5;64(1):122-7 PMID: 1170846
  13. Determination of the complete amino acid sequence of bovine cardiac troponin C.
    Biochemistry. 1976 Mar 9;15(5):1171-80 PMID: 1252434
  14. A fluorescence stopped flow analysis of Ca2+ exchange with troponin C.
    J Biol Chem. 1979 May 10;254(9):3497-502 PMID: 429366
  15. Chemically skinned mammalian skeletal muscle. I. The structure of skinned rabbit psoas.
    Tissue Cell. 1979;11(3):553-66 PMID: 494240
  16. The time-course of Ca2+ exchange with calmodulin, troponin, parvalbumin, and myosin in response to transient increases in Ca2+.
    Biophys J. 1981 Jun;34(3):559-69 PMID: 7195747
  17. Calmodulin-free skeletal-muscle troponin C prepared in the absence of urea.
    Biochem J. 1981 Apr 1;195(1):205-11 PMID: 6272746
  18. A structural role for the Ca2+-Mg2+ sites on troponin C in the regulation of muscle contraction. Preparation and properties of troponin C depleted myofibrils.
    J Biol Chem. 1982 Jul 10;257(13):7678-83 PMID: 6211445
  19. Improved methodology for analysis and quantitation of proteins on one-dimensional silver-stained slab gels.
    Anal Biochem. 1983 Mar;129(2):277-87 PMID: 6189421
  20. Structure of the calcium regulatory muscle protein troponin-C at 2.8 A resolution.
    Nature. 1985 Feb 21-27;313(6004):653-9 PMID: 3974698
  21. Bacterial expression and characterization of proteins derived from the chicken calmodulin cDNA and a calmodulin processed gene.
    J Biol Chem. 1985 Apr 25;260(8):4704-12 PMID: 2985564
  22. Three-dimensional structure of calmodulin.
    Nature. 1985 May 2-8;315(6014):37-40 PMID: 3990807
  23. Evidence that the Sr2+ activation properties of cardiac troponin C are altered when substituted into skinned skeletal muscle fibers.
    J Biol Chem. 1985 Dec 15;260(29):15687-93 PMID: 3934162
  24. Altered Ca2+ dependence of tension development in skinned skeletal muscle fibers following modification of troponin by partial substitution with cardiac troponin C.
    J Biol Chem. 1986 May 5;261(13):6096-9 PMID: 3700385
  25. Genetically engineered calmodulins differentially activate target enzymes.
    J Biol Chem. 1986 Jul 25;261(21):9896-903 PMID: 3460991
  26. Site-specific mutagenesis of the alpha-helices of calmodulin. Effects of altering a charge cluster in the helix that links the two halves of calmodulin.
    J Biol Chem. 1987 Mar 5;262(7):3278-84 PMID: 3029108
  27. The control of myocardial contraction with skeletal fast muscle troponin C.
    J Biol Chem. 1987 Apr 25;262(12):5815-22 PMID: 3571236
  28. The central helix of calmodulin functions as a flexible tether.
    J Biol Chem. 1988 Sep 5;263(25):12175-8 PMID: 3137220
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1990-12-00
Pages
9538-42
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC55207
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]