Proton transfer-mediated GPCR activation
Xuejun C. Zhang, Can Cao, Ye Zhou, Yan Zhao
Proton transfer-mediated GPCR activation
G-protein coupled receptors (GPCRs) play essential roles in signal transduction from the environment into the cell. While many structural features have been elucidated in great detail, a common functional mechanism on how the ligand-binding signal is converted into a conformational change on the cytoplasmic face resulting in subsequent activation of downstream effectors remain to be established. Based on available structural and functional data of the activation process in class-A GPCRs, we propose here that a change in protonation status, together with proton transfer via conserved structural elements located in the transmembrane region, are the key elements essential for signal transduction across the membrane.
GPCR / activation / protonation / membrane potential
[1] |
Angel TE, Chance MR, Palczewski K (2009) Conserved waters mediate structural and functional activation of family A (rhodopsin-like) G protein-coupled receptors. Proc Natl Acad Sci USA106(21): 8555-8560
CrossRef
Google scholar
|
[2] |
Ballesteros JA, Weinstein H (1995) Integrated methods for the construction of three dimensional models and computational probing of structure-function relations in G protein-coupled receptors. Methods Neurosci. 25: 366-428
CrossRef
Google scholar
|
[3] |
Beinborn M (2006) Class B GPCRs: A hidden agonist within? Mol Pharmacol70: 1-4 (Relates to article by Dong, et al. FastForward 10 March 2006)
|
[4] |
Bihoreau C
CrossRef
Google scholar
|
[5] |
Ceresa BP, Limbird LE (1994) Mutation of an aspartate residue highly conserved among G-protein-coupled receptors results in nonreciprocal disruption of alpha 2-adrenergic receptor-G-protein interactions. A negative charge at amino acid residue 79 forecasts alpha 2A-adrenergic receptor sensitivity to allosteric modulation by monovalent cations and fully effective receptor/Gprotein coupling. J Biol Chem269(47): 29557-29564
|
[6] |
Garczarek F
CrossRef
Google scholar
|
[7] |
Hanson MA, Stevens RC (2009) Discovery of new GPCR biology: one receptor structure at a time. Structure17(1): 8-14
CrossRef
Google scholar
|
[8] |
Hollenstein K
CrossRef
Google scholar
|
[9] |
Hollenstein K
CrossRef
Google scholar
|
[10] |
Hulme EC (2013) GPCR activation: a mutagenic spotlight on crystal structures. Trends Pharmacol Sci34(1): 67-84
CrossRef
Google scholar
|
[11] |
Insel PA
CrossRef
Google scholar
|
[12] |
Katritch V, Cherezov V, Stevens RC (2013) Structure-function of the G protein-coupled receptor superfamily. Annu Rev Pharmacol Toxicol53: 531-556
CrossRef
Google scholar
|
[13] |
Liu W
CrossRef
Google scholar
|
[14] |
Lohse MJ, Maiellaro I, Calebiro D (2014) Kinetics and mechanism of G protein-coupled receptor activation. Curr Opin Cell Biol27: 87-93
CrossRef
Google scholar
|
[15] |
Marie J
|
[16] |
Martin S
|
[17] |
Mitchell DC, Litman BJ (1999) Effect of protein hydration on receptor conformation: decreased levels of bound water promote metarhodopsin II formation. Biochemistry38(24): 7617-7623
CrossRef
Google scholar
|
[18] |
Nucci NV
CrossRef
Google scholar
|
[19] |
Onufriev A, Smondyrev A, Bashford D (2003) Proton affinity changes driving unidirectional proton transport in the bacteriorhodopsin photocycle. J Mol Biol332(5): 1183-1193
CrossRef
Google scholar
|
[20] |
Palczewski K
CrossRef
Google scholar
|
[21] |
Parent JL
CrossRef
Google scholar
|
[22] |
Payandeh J
CrossRef
Google scholar
|
[23] |
Proulx CD
CrossRef
Google scholar
|
[24] |
Rasmussen SG
CrossRef
Google scholar
|
[25] |
Rohrer DK, Kobilka BK (1998) G protein-coupled receptors: functional and mechanistic insights through altered gene expression. Physiol Rev78(1): 35-52
|
[26] |
Siu FY
CrossRef
Google scholar
|
[27] |
Strader CD
|
[28] |
Tadevosyan A
CrossRef
Google scholar
|
[29] |
Van Durme J
CrossRef
Google scholar
|
[30] |
Warne T
CrossRef
Google scholar
|
[31] |
White JF
CrossRef
Google scholar
|
[32] |
Wilson MH, Highfield HA, Limbird LE (2001) The role of a conserved inter-transmembrane domain interface in regulating alpha(2a)- adrenergic receptor conformational stability and cell-surface turnover. Mol Pharmacol59(4): 929-938
|
[33] |
Wootten D
CrossRef
Google scholar
|
[34] |
Xu F
CrossRef
Google scholar
|
[35] |
Zhang C et al (2012) High-resolution crystal structure of human protease-activated receptor 1. Nature492: 387-392
CrossRef
Google scholar
|
[36] |
Zhang XC
CrossRef
Google scholar
|
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