Menny A et al. (2017), Identification of a pre-active conformation of ...

XB-ART-54399

Elife 2017 Mar 15;6. doi: 10.7554/eLife.23955.

Show Gene links Show Anatomy links

Identification of a pre-active conformation of a pentameric channel receptor.

Menny A , Lefebvre SN , Schmidpeter PA , Drège E , Fourati Z , Delarue M , Edelstein SJ , Nimigean CM , Joseph D , Corringer PJ .

???displayArticle.abstract???
Pentameric ligand-gated ion channels (pLGICs) mediate fast chemical signaling through global allosteric transitions. Despite the existence of several high-resolution structures of pLGICs, their dynamical properties remain elusive. Using the proton-gated channel GLIC, we engineered multiple fluorescent reporters, each incorporating a bimane and a tryptophan/tyrosine, whose close distance causes fluorescence quenching. We show that proton application causes a global compaction of the extracellular subunit interface, coupled to an outward motion of the M2-M3 loop near the channel gate. These movements are highly similar in lipid vesicles and detergent micelles. These reorganizations are essentially completed within 2 ms and occur without channel opening at low proton concentration, indicating that they report a pre-active intermediate state in the transition pathway toward activation. This provides a template to investigate the gating of eukaryotic neurotransmitter receptors, for which intermediate states also participate in activation.

???displayArticle.pubmedLink??? 28294942
???displayArticle.pmcLink??? PMC5398890
???displayArticle.link??? Elife
???displayArticle.grants??? [+]

Genes referenced: ecd

???attribute.lit??? ???displayArticles.show???

	Figure 1. Structure of GLIC.(A) Positions for fluorophore and quencher insertion. Top panel: side view of GLIC crystalized at pH 7. Lower panel: Top-down view of GLIC. Insets show particular regions targeted for mBBr labeling. Positions where cysteines are engineered are represented in color and positions for tryptophan/tyrosine mutations are in black. All amino acids are represented by a sphere for the Cß carbon, to show the orientation of the side chain. Endogenous tryptophans and tyrosines are in stick representation. (B) X-ray structure of the V135C-Bimane. A top and side view are presented showing the localization of the two Bimane molecules resolved in the structure. Insets show a zoom for both the top and side view of the V135C-Bimane and the putative quencher W72. In the top zoom, the experimental 2Fo-Fc density map contoured at one sigma is shown in mesh for the Bimane.DOI: http://dx.doi.org/10.7554/eLife.23955.003
	Figure 2. Bimanes characteristics and labeling of GLIC-expressing cells.(A) Left: Structures of the Monobromo bimane (mBBr) and the bimane Bunte salt (BBs) before and after reaction with cysteines. Right: Excitation and emission spectra of both fluorophores and emission spectra of the mBBr (10 µM) after reaction with cysteines (1 mM), acidification of the medium (pH 4) or addition of tryptophan (25 mM). All spectra are normalized to the peak intensity of the mBBr emission spectrum. (B, C) Representative electrophysiological recordings of oocytes expressing GLIC Q193C mutant. Unless otherwise indicated, oocytes were perfused with a pH 7.3 solution. (B) Traces showing no functional inhibition of GLIC Q193C after mBBr exposure with acute (left) or prolonged application (right), whereas the same oocytes are inhibited by reaction with MMTS, which can be reversed by application of DTT. (C) Left: Trace showing the inhibition of GLIC Q193C after reaction with the MMTS but not the BBs after acute application. Right: Effective inhibition of GLIC Q193C after reaction with the BBs after the oocyte was incubated for 1 hr in presence of the fluorophore, followed by reduction of the Cys-BBs bond by DTT.DOI: http://dx.doi.org/10.7554/eLife.23955.004Figure 2—figure supplement 1. Bimane labeling of CHO cells.The pictures were taken on a confocal microscope with a 405 nm excitation laser and show GLIC D136C transfected cells, positive for the transfection marker mCherry (not shown). On the left panel, cells were labeled for 1 hr, on ice, with the qBBr, a commercially available ‘non-permeant’ bimane derivative. On the right panel, cells were labeled for 1 hr, on ice, with the BBs. The scale bar represents 20 µm.DOI: http://dx.doi.org/10.7554/eLife.23955.005
	Figure 2—figure supplement 2. 1HNMR (300 MHz, D2O) and 13C NMR (75 MHz, D2O/MeOD) spectra of the BBs.DOI: http://dx.doi.org/10.7554/eLife.23955.006
	Figure 2—figure supplement 3. Characterisation of the synthetized BBs. (A) RP-HPLC chromatogram and MS spectrum of bimane thiosulfonic acid. (B): HRMS (ESI) spectrum of bimane thiosulfonic acid.DOI: http://dx.doi.org/10.7554/eLife.23955.007
	Figure 2—figure supplement 4. Typical electrophysiological traces for each major quenching-pairs mutants of GLIC.On the left are recordings made before BBs labeling and on the right are recordings made for the same oocyte after a 1 hr BBs incubation, with the exception of the P250C mutant which showed an important run down (either with or without labeling) and for which two different representative oocytes are shown.DOI: http://dx.doi.org/10.7554/eLife.23955.008
	Figure 2—figure supplement 5. Immunolabeling of oocytes expressing GLIC WT and loss-of-function mutants.Oocytes were co-injected with GLIC-HA WT or loss-of-function mutants and GFP. Control oocytes were injected with GFP only. Immunolabeling was directed against the HA-tag. Labeling of receptors expressed at the membrane is shown in red and GFP expressed in the cytoplasm in shown in green. The scale bar represents 30 µm.DOI: http://dx.doi.org/10.7554/eLife.23955.009
	Figure 3. Steady-state variations of fluorescence of Bimane-GLIC mutants in detergent.Top: Cartoon view of two subunits of GLIC, all the sites of bimane labeling are represented by a colored sphere. (A, B, C, D, E, F): The data show the fluorescence peak values as a function of the proton concentration, normalized to the peak intensity after SDS treatment. The same color code as the top cartoon was used to indicate the site of bimane labeling for each graph. Within one graph, the major quenching pairs with or without quencher are shown in bold black caption and secondary tryptophan quenchers are captioned in grey. The symbol ø was used for recordings made on receptors baring no other mutation than the one for bimane labeling and for which no endogenous quenchers were identified; otherwise the later are indicated in bold black caption. For all the points, mean values are presented and error bars represent the standard deviations.DOI: http://dx.doi.org/10.7554/eLife.23955.012Figure 3—figure supplement 1. Spectral characteristics of mBBr and Bimane-GLIC mutants.(A) Excitation spectra of the mBBr (10 µM) ± Cys (100 µM), ± Trp (12.5 mM) and at different pHs. All spectra were normalized on the peak value of the mBBr pH 8 excitation spectrum. (B) Variations of peak intensity of Bimane-Cys (10 µM) (purple) and Bimane-Cys (10 µM) + Trp (12.5 mM) (orange) in solutions ranging from pH 9 to pH 2. All intensities are normalized on the Bimane-Cys pH 7.3 peak intensity. All the data presented are mean values and error bars were calculated as standard deviations (n = 3). (C) Background fluorescence when recording Bimane-GLIC. The figure represents superimposed emission spectra of the Cys-less GLIC (C27S) and the Bimane-136-W101 mutant at pH 7.3, either in detergent or after reconstitution in asolectin liposomes. For both mutants, proteins were treated with mBBr and subsequently purified by gel filtration to remove unreacted fluorophore.DOI: http://dx.doi.org/10.7554/eLife.23955.013
	Figure 3—figure supplement 2. Emission spectra of Bimane-GLIC mutants in detergent.For each mutant, the graph on the left represents representative emission spectra recorded at different pHs and in presence of 1% SDS used as a denaturing agent; the graph on the right represents the same samples after they were individually brought back to pH 7.3 (the 1% SDS spectrum is left for comparison). All axis labels are identical between graphs and were shown only on one graph for clarity.DOI: http://dx.doi.org/10.7554/eLife.23955.014
	Figure 4. Effects of amino acid protonation and propofol on the fluorescence variations.(A) Top: Fluorescence intensities of the mutants Bimane-135-W72 and Bimane-135-W72-E67Q-E75Q-D91N normalized on each mutant’s intensity at pH 7.3. Bottom, from left to right: Top view of the extracellular domain of GLIC Bimane-C135 showing one subunit in light blue, and the Bimane-C135 (green), E67, E75 and D91 (red) in stick representation; zoom on the subunits interface of the ECD, top view; zoom on the subunits interface viewed from the inside of the ECD. (B) For each pH, fluorescence recordings of Bimane-labeled mutants were first made without propofol, followed by addition of propofol at 100 µM final concentration and re-recording of the same samples. All the data were normalized on the value of fluorescence at pH 7.3 without propofol. For all the data, mean values are presented and error bars are calculated as standard deviations (n = 3 to 6).DOI: http://dx.doi.org/10.7554/eLife.23955.015
	Figure 5. Steady-state fluorescence of Bimane-GLIC in liposomes.(A,B,C,D,E,F) The data show the fluorescence peak value for a given pH, normalized to the peak intensity of each mutant at the highest pH recorded (pH 8 or 7.3). Black lines represent the fluorescence values in liposomes and grey lines in detergent, for comparison. Plain lines represent the major fluorescent sensor and dashed lines the corresponding mutant in absence of quencher. The symbol ø was used for recordings made on receptors baring no other mutation than the one for bimane labeling and for which no endogenous quenchers were identified; otherwise the later are indicated in black caption. For all the data, mean values are presented and error bars are calculated as standard deviations.DOI: http://dx.doi.org/10.7554/eLife.23955.016
	Figure 6. Stopped-flow fluorescence measurements.(A) Each panel shows representative traces of the major quenching mutants with a zoom on the first 500 ms (left) and the entire recording (right). All traces are fitted to a multi-exponential (see Methods) represented in red. The color code is identical in each panel with a blue gradient starting from pH 6 (dark) to pH 4 (light). The red dash line represents the starting fluorescence at pH 8 after normalization, for the raw pH 8 trace see Figure 6—figure supplement 1. (B) Binning of τ values extracted from the stopped-flow multi-exponential fit (all pHs and all constructs were used for the plot). The log time binning interval is of 0.4 and the resulting bins are shown by red dashed lines on the plot. The distribution shows three major clusters for which the according τ value is indicated on the plot. (C) Fluorescence variations (calculated as a % of the overall variation at 30 s) for each time interval extracted from the binning plot. In this graph, mean values are presented and error bars are calculated as standard deviations.DOI: http://dx.doi.org/10.7554/eLife.23955.019Figure 6—figure supplement 1. Residuals of the stopped-flow data fits and pH 8 recordings.Residuals plots: The figure shows an example for each mutant and pH recorded, chosen at random. The time axis (x) is represented in log scale for better visualization of the first milliseconds. pH 8 recordings: The figure shows non-treated, raw stopped-flow recordings of GLIC mutants at pH 8, chosen at random. The axis labels are the same for all the residuals plots and pH 8 raw data, respectively, and were represented only once for clarity. A.U. stands for arbitrary unit.DOI: http://dx.doi.org/10.7554/eLife.23955.020
	Figure 7. Comparison of GLIC motions and function.(A) Fits to the Hill equation of fluorescence values in asolectin liposomes (black) and rate values extracted from the thallium flux assay (pink), both normalized to their respective maximum, for the Bimane-136-W101 mutant (n = 3). For comparison the ΔIf (thallium flux assay) curve of GLIC Cys-less is shown in grey (n = 3). (B) Stopped-flow recordings of the thallium fluxes quenching assay for the Bimane-136-W101 mutant. The pre-mix time was 15 ms for the empty and pH 5.2 liposomes and of 15.5 ms for the pH 4.5 and 4.2 recordings. (C) Fits to the Hill equation for electrophysiological currents (red) and fluorescence values in asolectin liposomes (black) for all major quenching pair mutants. The current and fluorescence are normalized to their respective maximum; pH 3.7 current values were excluded from the fits for mutants Bimane-250-Y197 and Bimane-33-W160 as they were systematically smaller than the maximal current. For all the data except panel B, mean values are presented and error bars are calculated as standard deviations.DOI: http://dx.doi.org/10.7554/eLife.23955.022Figure 7—figure supplement 1. Thallium flux assay.(A) The figure shows raw, non-treated, recordings of ANTS encapsulated in proteoliposomes carrying either the GLIC Cys-less (left) or the GLIC mutant Bimane-136-W101 (right), at different pHs. The pre-mix times (times for which the liposomes are in presence of proton before addition of thallium) after which the fluorescence was recorded is indicated on the side of each trace. The black traces show the recordings of ANTS-containing liposomes without any receptors. (B) The figure shows plots of ANTS quenching by thallium rates as a function of the pre-mix times, for GLIC Cys-less (left) and GLIC Bimane-136-W101 (right). The purple trace shows the rates measured at pH 4.2 in presence of the pore blocker picrotoxinin (PTX) at 400 µM. In these graphs, mean values are presented, the error bars represent the standard deviation and measurement were done with n = 4 to 6.DOI: http://dx.doi.org/10.7554/eLife.23955.023
	Figure 8. Conformational motions summary.(A) Global and zoomed in view of the GLICpH 7 structure, representing only two subunits, with the left structures viewed from the outside of the pentamer and the right structures from the inside. All major quenching pairs are represented by a sphere, colored for the mutation to cysteine and bimane labeling, and black for the corresponding quencher. All pairs are captioned in the same color and joined by a red line. (B) Hypothetic kinetic scheme for the GLIC structural reorganizations. The large arrows represent the major recorded fluorescence variations and the small arrows represent minor variations.DOI: http://dx.doi.org/10.7554/eLife.23955.024
	Author response image 1. Characteristics of proteoliposomes used for Bimane quenching studies.(A) SDS-PAGE gel fluorescence scan (left) and labeling quantification (right) of GLIC mutants D136C and T219C reconstituted in liposomes (PL) or in detergent (DDM) and labeled with Alexa Fluor 546. (B) Dynamic light scattering profile of GLIC proteoliposomes. The peaks are represented with the standard radius-weighted intensity and the radius on a log scale. The first peak represents GLIC proteoliposomes (which are the major species of objects) and the second peak represents aggregates (very minor species). (C) Emission spectra of the HPTS fluorophore in proteoliposome buffer, excited at 372 nm at pH 7.3 and pH 4. (D) Stopped-flow recordings of HTPS loaded GLIC proteoliposomes (left) or empty liposomes (right). The lower left panel shows a zoom of the first second of the GLIC proteoliposomes recordings, represented using a log scale for better visualization of the first milliseconds. For all recordings, the excitation was set at 372 nm and the fluorescence recorded through a 505 nm high-pass filter after a 2.1 ms mixing dead-time to reach either pH 7.3 or pH 4.DOI: http://dx.doi.org/10.7554/eLife.23955.026

References [+] :

Althoff, X-ray structures of GluCl in apo states reveal a gating mechanism of Cys-loop receptors. 2014, Pubmed