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The Role of Tropomyosin and Cardiac Myosin Binding Protein-C in Modulating Thin Filament Activity

Inchingolo, Alessio Vincenzo (2019) The Role of Tropomyosin and Cardiac Myosin Binding Protein-C in Modulating Thin Filament Activity. Doctor of Philosophy (PhD) thesis, University of Kent,. (KAR id:72483)

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Abstract

Muscle contraction is a finely tuned mechanism involving cyclical interactions between

actin and myosin, regulated by calcium through troponin and tropomyosin and

modulated by myosin binding protein-C. Genetic mutations of the proteins involved in

such complex mechanism can thus lead to potential life threatening diseases, such as

Hypertrophic Cardiomyopathy (HCM). Although being mostly asymptomatic, HCM

affects 1 in 500 people, ultimately leading to poor prognosis and sudden death,

thought to occur through the impairment of relaxation during diastole.

In this thesis I present the experiments conducted to improve our current

understanding of the molecular mechanism behind HCM, specifically on the role of

tropomyosin and myosin binding protein-C in modulating thin filament activation and

relaxation. Using a single molecule approach, we first visualised fluorescent myosin

binding to reconstituted thin filaments and examined their dynamics in the presence

of the tropomyosin HCM causing E180G mutation, demonstrating a shift of the thin

filament activation state towards the closed state, facilitating myosin binding at low

calcium, and a reduction of the thin filament regulatory unit.

We then looked at the dynamics of very highly concentrated clusters of myosin,

showing how the sudden collapse of these active regions cannot be explained by

normal relaxation mechanisms, thus suggesting an alternative mechanistic role for

tropomyosin and how its mutations could lead to impaired relaxation in HCM.

Finally, we turned our focus on N-terminal fragments of cardiac myosin binding

protein-C (cMyBP-C) and study their role in thin filament activation, by looking at how

they affect acto-myosin interactions. We found that only the presence of the whole

cMyBP-C N-terminus was able to promote acto-myosin interactions at low Ca2+ or

repressing them at high Ca2+. Moreover, by looking at the dynamics of the fragments,

we were able to determine that cMyBP-C possesses a two steps binding mechanism to

actin, leading us to define its mechanism by which it activates the thin filament.

Item Type: Thesis (Doctor of Philosophy (PhD))
Divisions: Divisions > Division of Natural Sciences > Biosciences
SWORD Depositor: System Moodle
Depositing User: System Moodle
Date Deposited: 14 Feb 2019 10:10 UTC
Last Modified: 20 May 2021 13:26 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/72483 (The current URI for this page, for reference purposes)
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