TY - JOUR
T1 - A biophysical perspective of the regulatory mechanisms of ezrin/radixin/moesin proteins
AU - Senju, Yosuke
AU - Tsai, Feng Ching
N1 - Funding Information:
We thank Prof. Pekka Lappalainen (HiLIFE - Institute of Biotechnology, University of Helsinki, Finland), Prof. Patricia Bassereau (Institut Curie, France), Prof. Emmanuel Lemichez (Institut Pasteur, France), and Prof. Ilpo Vattulainen (Department of Physics, University of Helsinki, Finland) for the insightful discussions.
Funding Information:
This study was supported by the FY 2015 Researcher Exchange Program between the Japan Society for the Promotion of Science (JSPS) and Academy of Finland (AF), Astellas Foundation for Research on Metabolic Disorders, Scandinavia-Japan Sasakawa Foundation, Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical Care, The Association for Fordays Self-Reliance Support in Japan, Okayama Foundation for Science and Technology, ONO Medical Research Foundation, Takeda Science Foundation, The Naito Foundation, The Company of Biologists, European Biophysical Societies Association (EBSA), and Institut Curie, Centre National de la Recherche Scientifique (CNRS).
Publisher Copyright:
© 2022, International Union for Pure and Applied Biophysics (IUPAB) and Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/2
Y1 - 2022/2
N2 - Many signal transductions resulting from ligand–receptor interactions occur at the cell surface. These signaling pathways play essential roles in cell polarization, membrane morphogenesis, and the modulation of membrane tension at the cell surface. However, due to the large number of membrane-binding proteins, including actin-membrane linkers, and transmembrane proteins present at the cell surface, the molecular mechanisms underlying the regulation at the cell surface are yet unclear. Here, we describe the molecular functions of one of the key players at the cell surface, ezrin/radixin/moesin (ERM) proteins from a biophysical point of view. We focus our discussion on biophysical properties of ERM proteins revealed by using biophysical tools in live cells and in vitro reconstitution systems. We first describe the structural properties of ERM proteins and then discuss the interactions of ERM proteins with PI(4,5)P2 and the actin cytoskeleton. These properties of ERM proteins revealed by using biophysical approaches have led to a better understanding of their physiological functions in cells and tissues.
AB - Many signal transductions resulting from ligand–receptor interactions occur at the cell surface. These signaling pathways play essential roles in cell polarization, membrane morphogenesis, and the modulation of membrane tension at the cell surface. However, due to the large number of membrane-binding proteins, including actin-membrane linkers, and transmembrane proteins present at the cell surface, the molecular mechanisms underlying the regulation at the cell surface are yet unclear. Here, we describe the molecular functions of one of the key players at the cell surface, ezrin/radixin/moesin (ERM) proteins from a biophysical point of view. We focus our discussion on biophysical properties of ERM proteins revealed by using biophysical tools in live cells and in vitro reconstitution systems. We first describe the structural properties of ERM proteins and then discuss the interactions of ERM proteins with PI(4,5)P2 and the actin cytoskeleton. These properties of ERM proteins revealed by using biophysical approaches have led to a better understanding of their physiological functions in cells and tissues.
KW - Actin cytoskeleton
KW - Ezrin/radixin/moesin proteins
KW - GUVs
KW - Membrane tension
KW - Phosphatidylinositol 4,5-bisphosphate
KW - Supported lipid bilayers
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U2 - 10.1007/s12551-021-00928-0
DO - 10.1007/s12551-021-00928-0
M3 - Review article
AN - SCOPUS:85123821248
SN - 1867-2450
VL - 14
SP - 199
EP - 208
JO - Biophysical Reviews
JF - Biophysical Reviews
IS - 1
ER -