Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene-Reference-Cited by-同舟云学术

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Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene

Published:2017-12 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Borovikov Yurii S.,Rysev Nikita A.,Karpicheva Olga E.,Sirenko Vladimir V.,Avrova Stanislava V.,Piers Adam,Redwood Charles S.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-17076-9.pdf

Reference31 articles.

1. Gordon, A. M., Homsher, E. & Regnier, M. Regulation of contraction in striated muscle. Physiol. Rev. 80, 853–924 (2000).

2. Perry, S. V. Vertebrate TM: distribution, properties and function. J. Muscle Res. Cell. Motil. 22, 5–49 (2001).

3. Borovikov, Y. S., Karpicheva, O. E., Avrova, S. V. & Redwood, C. S. Modulation of the effects of tropomyosin on actin and myosin conformational changes by troponin and Ca2+. Biochim. Biophys. Acta 1794, 985–994 (2009).

4. Borovikov, Y. S. et al. Molecular mechanisms of deregulation of the thin filament associated with the R167H and K168E substitutions in Tpm1.1. Arch. Biochem. Biophys. 614, 28–40 (2017).

5. Lehman, W., Orzechowski, M., Li, X. E., Fischer, S. & Raunser, S. J. Gestalt-binding of tropomyosin on actin during thin filament activation. Muscle Res. Cell Motil. 34, 155–163 (2013).

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