Strength in numbers: effect of protein crowding on the shape of cell membranes
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Strength in numbers : effect of protein crowding on the shape of cell membranes. / Ruhoff, Victoria Thusgaard; Moreno-Pescador, Guillermo; Pezeshkian, Weria; Bendix, Poul Martin.
In: Biochemical Society Transactions, Vol. 50, No. 5, 31.10.2022, p. 1257-1267.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Strength in numbers
T2 - effect of protein crowding on the shape of cell membranes
AU - Ruhoff, Victoria Thusgaard
AU - Moreno-Pescador, Guillermo
AU - Pezeshkian, Weria
AU - Bendix, Poul Martin
N1 - Publisher Copyright: © 2022 The Author(s).
PY - 2022/10/31
Y1 - 2022/10/31
N2 - Continuous reshaping of the plasma membrane into pleomorphic shapes is critical for a plethora of cellular functions. How the cell carries out this enigmatic control of membrane remodeling has remained an active research field for decades and several molecular and biophysical mechanisms have shown to be involved in overcoming the energy barrier associated with membrane bending. The reported mechanisms behind membrane bending have been largely concerned with structural protein features, however, in the last decade, reports on the ability of densely packed proteins to bend membranes by protein-protein crowding, have challenged prevailing mechanistic views. Crowding has now been shown to generate spontaneous vesicle formation and tubular morphologies on cell- and model membranes, demonstrating crowding as a relevant player involved in the bending of membranes. Still, current research is largely based on unnatural overexpression of proteins in non-native domains, and together with efforts in modeling, this has led to questioning the in vivo impact of crowding. In this review, we examine this previously overlooked mechanism by summarizing recent advances in the understanding of protein-protein crowding and its prevalence in cellular membrane-shaping processes.
AB - Continuous reshaping of the plasma membrane into pleomorphic shapes is critical for a plethora of cellular functions. How the cell carries out this enigmatic control of membrane remodeling has remained an active research field for decades and several molecular and biophysical mechanisms have shown to be involved in overcoming the energy barrier associated with membrane bending. The reported mechanisms behind membrane bending have been largely concerned with structural protein features, however, in the last decade, reports on the ability of densely packed proteins to bend membranes by protein-protein crowding, have challenged prevailing mechanistic views. Crowding has now been shown to generate spontaneous vesicle formation and tubular morphologies on cell- and model membranes, demonstrating crowding as a relevant player involved in the bending of membranes. Still, current research is largely based on unnatural overexpression of proteins in non-native domains, and together with efforts in modeling, this has led to questioning the in vivo impact of crowding. In this review, we examine this previously overlooked mechanism by summarizing recent advances in the understanding of protein-protein crowding and its prevalence in cellular membrane-shaping processes.
KW - bending mechanism
KW - entropic pressure
KW - excluded volume
KW - membrane curvature
KW - membrane proteins
KW - protein crowding
U2 - 10.1042/BST20210883
DO - 10.1042/BST20210883
M3 - Journal article
C2 - 36214373
AN - SCOPUS:85141003453
VL - 50
SP - 1257
EP - 1267
JO - Biochemical Society Transactions
JF - Biochemical Society Transactions
SN - 0300-5127
IS - 5
ER -
ID: 325073908