Mechanical Force and Cytoplasmic Ca2+ Activate Yeast TRPY1 in Parallel

Mechanical Force and Cytoplasmic Ca2+ Activate Yeast TRPY1 in Parallel The ability to sense mechanical and osmotic stimuli is vital to all organisms from mammals to bacteria. Members of the transient receptor potential (TRP) ion-channel family have attracted intense attention for their involvement in mechanosensation. The yeast homologue TRPY1 can clearly be activated by hypertonic shock in vivo and by stretch force under patch clamp. Like its animal counterparts, TRPY1 is polymodal, being gated by membrane stretch force and by cytoplasmic Ca2+. Here, we investigated how these two gating principles interact. We found that stretch force can induce some channel activation without cytoplasmic Ca2+. Tens of micromolar Ca2+ greatly enhance the observed force-induced activities, with open probabilities following well the Boltzmann distribution, in which the two gating energies are summed as exponents. To map this formalism to structures, we found Ca2+-binding proteins such as calmodulin or calcineurin to be unnecessary. However, removing a dense cluster of negative charges in the C-terminal cytoplasmic domain of TRPY1 greatly diminishes the Ca2+ activation as well as its influence on force activation. We also found a strategic point upstream of this charge cluster, at which insertion of amino acids weakens Ca2+ activation considerably but leaves the mechanosensitivity nearly intact. These results led to a structure–function model in which Ca2+ binding to the cytoplasmic domain and stretching of the membrane-embedded domain both generate gating force, reaching the gate in parallel. The Journal of Membrane Biology Springer Journals

Mechanical Force and Cytoplasmic Ca2+ Activate Yeast TRPY1 in Parallel

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Copyright © 2009 by Springer Science+Business Media, LLC
Life Sciences; Human Physiology ; Biochemistry, general
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