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Ultrastructural and kinetic evidence support that thick filaments slide through the Z-disc

Andre Tomalka, Maximilian Heim, Annika Klotz,Christian Rode,Tobias Siebert

Journal of the Royal Society, Interface(2022)

Cited 2|Views4
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Abstract
How myofilaments operate at short mammalian skeletal muscle lengths is unknown. A common assumption is that thick (myosin-containing) filaments get compressed at the Z-disc. We provide ultrastructural evidence of sarcomeres contracting down to 0.44 mu m-approximately a quarter of thick filament resting length-in long-lasting contractions while apparently keeping a regular, parallel thick filament arrangement. Sarcomeres produced force at such extremely short lengths. Furthermore, sarcomeres adopted a bimodal length distribution with both modes below lengths where sarcomeres are expected to generate force in classic force-length measurements. Mammalian fibres did not restore resting length but remained short after deactivation, as previously reported for amphibian fibres, and showed increased forces during passive re-elongation. These findings are incompatible with viscoelastic thick filament compression but agree with predictions of a model incorporating thick filament sliding through the Z-disc. This more coherent picture of mechanical mammalian skeletal fibre functioning opens new perspectives on muscle physiology.
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Key words
skeletal muscle fibre,myosin,actin,titin,delta-state,muscle physiology,structural biology
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