TY - JOUR
T1 - Lipid-mediated prestin organization in outer hair cell membranes and its implications in sound amplification
AU - Dehghani-Ghahnaviyeh, Sepehr
AU - Zhao, Zhiyu
AU - Tajkhorshid, Emad
N1 - The authors acknowledge stimulating conversations and discussion with Drs. E. Gouaux, J. Ge, and J. Elferich at Vollum Institute, Oregon Health & Science University. This research is supported by National Institutes of Health grants R01-GM123455 and P41-GM104601 (to E.T.). Simulations in this study have been performed using allocations at National Science Foundation Supercomputing Centers (XSEDE grant number MCA06N060), and the Blue Waters Petascale Computing Facility of National Center for Supercomputing Applications (NCSA) at University of Illinois at Urbana-Champaign, which is supported by the National Science Foundation (awards OCI-0725070 and ACI-1238993) and the state of Illinois.
The authors acknowledge stimulating conversations and discussion with Drs. E. Gouaux, J. Ge, and J. Elferich at Vollum Institute, Oregon Health & Science University. This research is supported by National Institutes of Health grants R01-GM123455 and P41-GM104601 (to E.T.). Simulations in this study have been performed using allocations at National Science Foundation Supercomputing Centers (XSEDE grant number MCA06N060), and the Blue Waters Petascale Computing Facility of National Center for Supercomputing Applications (NCSA) at University of Illinois at Urbana-Champaign, which is supported by the National Science Foundation (awards OCI-0725070 and ACI-1238993) and the state of Illinois.
PY - 2022/12
Y1 - 2022/12
N2 - Prestin is a high-density motor protein in the outer hair cells (OHCs), whose conformational response to acoustic signals alters the shape of the cell, thereby playing a major role in sound amplification by the cochlea. Despite recent structures, prestin’s intimate interactions with the membrane, which are central to its function remained unresolved. Here, employing a large set (collectively, more than 0.5 ms) of coarse-grained molecular dynamics simulations, we demonstrate the impact of prestin’s lipid-protein interactions on its organization at densities relevant to the OHCs and its effectiveness in reshaping OHCs. Prestin causes anisotropic membrane deformation, which mediates a preferential membrane organization of prestin where deformation patterns by neighboring copies are aligned constructively. The resulting reduced membrane rigidity is hypothesized to maximize the impact of prestin on OHC reshaping. These results demonstrate a clear case of protein-protein cooperative communication in membrane, purely mediated by interactions with lipids.
AB - Prestin is a high-density motor protein in the outer hair cells (OHCs), whose conformational response to acoustic signals alters the shape of the cell, thereby playing a major role in sound amplification by the cochlea. Despite recent structures, prestin’s intimate interactions with the membrane, which are central to its function remained unresolved. Here, employing a large set (collectively, more than 0.5 ms) of coarse-grained molecular dynamics simulations, we demonstrate the impact of prestin’s lipid-protein interactions on its organization at densities relevant to the OHCs and its effectiveness in reshaping OHCs. Prestin causes anisotropic membrane deformation, which mediates a preferential membrane organization of prestin where deformation patterns by neighboring copies are aligned constructively. The resulting reduced membrane rigidity is hypothesized to maximize the impact of prestin on OHC reshaping. These results demonstrate a clear case of protein-protein cooperative communication in membrane, purely mediated by interactions with lipids.
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U2 - 10.1038/s41467-022-34596-9
DO - 10.1038/s41467-022-34596-9
M3 - Article
C2 - 36371434
AN - SCOPUS:85141697130
SN - 2041-1723
VL - 13
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 6877
ER -