Abstract

The indirect flight muscle of insects (IFM), such as Drosophila and Lethocerus, is activated by periodic stretches at a priming concentration of calcium. The alternate activation of opposing muscles produces the rapid wing movements needed for flight. Cardiac muscle develops more force at longer sarcomere lengths (length-dependent activation), and force is enhanced by a rapid stretch at each beat. Troponin bridges between thick and thin filaments have been identified in Lethocerus IFM (Perz-Edwards et al, 2014) and these may be stretch sensors. Cardiac TnC and the TnC-F2 isoform in IFM both bind one regulatory calcium in the N-lobe. The force-pCa curve for IFM with only the TnC-F2 isoform (pCa50 5.8 and co-operativity nH 3.2) is similar to that of cardiac trabeculae, suggesting the co-operative behaviour is produced in the same way. TnC-F1, the IFM isoform needed for stretch activation, binds one calcium in the C-lobe, which is not regulatory. The force-pCa curve for IFM fibres, in which TnC-F1 is the main isoform, shows greater calcium-sensitivity and less co-operativity (pCa50 6.2, nH 1.3). The force-pCa curve of IFM fibres is similar to that of cardiac trabeculae with bound C1-C2 fragment of MyBP-C, in which calcium-sensitivity is increased and co-operativity greatly reduced. In this case, cardiac and IFM fibres achieve the same mechanical properties by different mechanisms. In order to determine if troponin forms part of a link between thick and thin filaments in IFM, we have tested binding between a tropomyosin-troponin complex and isolated thick filaments or myosin. The subunits of tropomyosin-troponin and the conditions needed for binding will be described.

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