TY - JOUR
T1 - Functional dynamics of cell surface membrane proteins
AU - Nishida, Noritaka
AU - Osawa, Masanori
AU - Takeuchi, Koh
AU - Imai, Shunsuke
AU - Stampoulis, Pavlos
AU - Kofuku, Yutaka
AU - Ueda, Takumi
AU - Shimada, Ichio
N1 - Funding Information:
This work was supported in part by Grants from the Japan New Energy and Industrial Technology Development Organization (NEDO) and the Ministry of Economy, Trade, and Industry (METI) (to I.S.), a Grant-in-Aid for Scientific Research on Priority Areas from the Japanese Ministry of Education, Culture, Sports, Science, and Technology (to M.O., K.T., T.U., and I.S.), and a Grant from Takeda Science Foundation (to M.O.).
PY - 2014/4
Y1 - 2014/4
N2 - Cell surface receptors are integral membrane proteins that receive external stimuli, and transmit signals across plasma membranes. In the conventional view of receptor activation, ligand binding to the extracellular side of the receptor induces conformational changes, which convert the structure of the receptor into an active conformation. However, recent NMR studies of cell surface membrane proteins have revealed that their structures are more dynamic than previously envisioned, and they fluctuate between multiple conformations in an equilibrium on various timescales. In addition, NMR analyses, along with biochemical and cell biological experiments indicated that such dynamical properties are critical for the proper functions of the receptors. In this review, we will describe several NMR studies that revealed direct linkage between the structural dynamics and the functions of the cell surface membrane proteins, such as G-protein coupled receptors (GPCRs), ion channels, membrane transporters, and cell adhesion molecules.
AB - Cell surface receptors are integral membrane proteins that receive external stimuli, and transmit signals across plasma membranes. In the conventional view of receptor activation, ligand binding to the extracellular side of the receptor induces conformational changes, which convert the structure of the receptor into an active conformation. However, recent NMR studies of cell surface membrane proteins have revealed that their structures are more dynamic than previously envisioned, and they fluctuate between multiple conformations in an equilibrium on various timescales. In addition, NMR analyses, along with biochemical and cell biological experiments indicated that such dynamical properties are critical for the proper functions of the receptors. In this review, we will describe several NMR studies that revealed direct linkage between the structural dynamics and the functions of the cell surface membrane proteins, such as G-protein coupled receptors (GPCRs), ion channels, membrane transporters, and cell adhesion molecules.
KW - Cell surface receptors
KW - Dynamics
KW - Membrane proteins
KW - NMR
UR - http://www.scopus.com/inward/record.url?scp=84897002636&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84897002636&partnerID=8YFLogxK
U2 - 10.1016/j.jmr.2013.11.007
DO - 10.1016/j.jmr.2013.11.007
M3 - Article
C2 - 24331735
AN - SCOPUS:84897002636
SN - 1090-7807
VL - 241
SP - 86
EP - 96
JO - Journal of Magnetic Resonance
JF - Journal of Magnetic Resonance
IS - 1
ER -