Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle

Journal article

To understand the molecular mechanism by which the hypertrophic cardiomyopathy-causing Asp175Asn and Glu180Gly mutations in α-tropomyosin alter contractile regulation, we labeled recombinant wild type and mutant α-tropomyosins with 5-iodoacetamide-fluorescein and incorporated them into the ghost muscle fibers. The orientation and mobility of the probe were studied by polarized fluorimetry at different stages of the ATPase cycle. Multistep alterations in the position and mobility of wild type tropomyosin on the thin filaments during the ATP cycle were observed. Both mutations were found to shift tropomyosin strands further towards the open position and to change the affinity of tropomyosin for actin, with the effect of the Glu180Gly mutation being greater than Asp175Asn, showing an increase in the binding strong cross-bridges to actin during the ATPase cycle. These structural changes to the thin filament are likely to underlie the observed increased Ca 2+-sensitivity caused by these mutations which initiates the disease remodeling. © 2011 Elsevier Inc.

Authors: Borovikov, Y; Rysev, N; Karpicheva, O; Redwood, C

• Journal: Biochemical and Biophysical Research Communications
• Volume: 407
• Issue: 1
• Pages: 197-201
• Publication date: 2011-04-01
• DOI: 10.1016/j.bbrc.2011.02.139
• EISSN: 1090-2104
• ISSN: 0006-291X
• Language: English
• Keywords: Hypertrophic cardiomyopathy; Ghost muscle fibers; Polarized fluorescence; ATPase cycle; α-Tropomyosin