scholarly journals Solution Structure of the Gloeobacter Violaceus Ligand-Gated Ion Channel Probed by Small-Angle Neutron Scattering

2021 ◽  
Vol 120 (3) ◽  
pp. 56a
Author(s):  
Marie Lycksell ◽  
Urska Rovsnik ◽  
Cathrine C. Bergh ◽  
Nicolai T. Johansen ◽  
Anne Martel ◽  
...  
2021 ◽  
Vol 118 (37) ◽  
pp. e2108006118
Author(s):  
Marie Lycksell ◽  
Urška Rovšnik ◽  
Cathrine Bergh ◽  
Nicolai T. Johansen ◽  
Anne Martel ◽  
...  

Pentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle neutron scattering (SANS) to probe ambient solution-phase properties of the pH-gated bacterial ion channel GLIC under resting and activating conditions. Data collection was optimized by inline paused-flow size-exclusion chromatography, and exchanging into deuterated detergent to hide the micelle contribution. Resting-state GLIC was the best-fit crystal structure to SANS curves, with no evidence for divergent mechanisms. Moreover, enhanced-sampling molecular-dynamics simulations enabled differential modeling in resting versus activating conditions, with the latter corresponding to an intermediate ensemble of both the extracellular and transmembrane domains. This work demonstrates state-dependent changes in a pentameric ion channel by SANS, an increasingly accessible method for macromolecular characterization with the coming generation of neutron sources.


2021 ◽  
Author(s):  
Marie Lycksell ◽  
Urška Rovšnik ◽  
Cathrine Bergh ◽  
Nicolai T Johansen ◽  
Anne Martel ◽  
...  

AbstractPentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle neutron scattering (SANS) to probe ambient solution-phase properties of the pH-gated bacterial ion channel GLIC under resting and activating conditions. Data collection was optimized by inline paused-flow size-exclusion chromatography, and exchanging into deuterated detergent to hide the micelle contribution. Resting-state GLIC was the best-fit crystal structure to SANS curves, with no evidence for divergent mechanisms. Moreover, enhanced-sampling molecular dynamics simulations enabled differential modeling in resting versus activating conditions, with the latter corresponding to an intermediate ensemble of both the extracellular and transmembrane domains. This work demonstrates state-dependent changes in a pentameric ion channel by SANS, an increasingly accessible method for macromolecular characterization with the coming generation of neutron sources.


2020 ◽  
Vol 236 ◽  
pp. 03003
Author(s):  
Jayesh S. Bhatt

An introductory account of using molecular simulations to deduce solution structure of macromolecules using small angle neutron scattering data is presented for biologists. The presence of a liquid solution provides mobility to the molecules, making it difficult to pin down their structure. Here a simple introduction to molecular dynamics and Monte Carlo techniques is followed by a recipe to use the output of the simulations along with the scattering data in order to infer the structure of macromolecules when they are placed in a liquid solution. Some practical issues to be watched for are also highlighted.


2006 ◽  
Vol 281 (50) ◽  
pp. 38266-38275 ◽  
Author(s):  
Indrajeet Singh ◽  
Harish Shankaran ◽  
Mark E. Beauharnois ◽  
Zhihua Xiao ◽  
Paschalis Alexandridis ◽  
...  

2018 ◽  
Vol 114 (3) ◽  
pp. 602-608 ◽  
Author(s):  
Swe-Htet Naing ◽  
Ryan C. Oliver ◽  
Kevin L. Weiss ◽  
Volker S. Urban ◽  
Raquel L. Lieberman

2000 ◽  
Vol 276-278 ◽  
pp. 528-529
Author(s):  
J Holzinger ◽  
H Heumann ◽  
E Manakova ◽  
M Rößle ◽  
K Vanatalu ◽  
...  

IUCrJ ◽  
2018 ◽  
Vol 5 (6) ◽  
pp. 780-793 ◽  
Author(s):  
Andreas Haahr Larsen ◽  
Jerzy Dorosz ◽  
Thor Seneca Thorsen ◽  
Nicolai Tidemand Johansen ◽  
Tamim Darwish ◽  
...  

The AMPA receptor GluA2 belongs to the family of ionotropic glutamate receptors, which are responsible for most of the fast excitatory neuronal signalling in the central nervous system. These receptors are important for memory and learning, but have also been associated with brain diseases such as Alzheimer's disease and epilepsy. Today, one drug is on the market for the treatment of epilepsy targeting AMPA receptors, i.e. a negative allosteric modulator of these receptors. Recently, crystal structures and cryo-electron microscopy (cryo-EM) structures of full-length GluA2 in the resting (apo), activated and desensitized states have been reported. Here, solution structures of full-length GluA2 are reported using small-angle neutron scattering (SANS) with a novel, fully matched-out detergent. The GluA2 solution structure was investigated in the resting state as well as in the presence of AMPA and of the negative allosteric modulator GYKI-53655. In solution and at neutral pH, the SANS data clearly indicate that GluA2 is in a compact form in the resting state. The solution structure resembles the crystal structure of GluA2 in the resting state, with an estimated maximum distance (D max) of 179 ± 11 Å and a radius of gyration (R g) of 61.9 ± 0.4 Å. An ab initio model of GluA2 in solution generated using DAMMIF clearly showed the individual domains, i.e. the extracellular N-terminal domains and ligand-binding domains as well as the transmembrane domain. Solution structures revealed that GluA2 remained in a compact form in the presence of AMPA or GYKI-53655. At acidic pH only, GluA2 in the presence of AMPA adopted a more open conformation of the extracellular part (estimated D max of 189 ± 5 Å and R g of 65.2 ± 0.5 Å), resembling the most open, desensitized class 3 cryo-EM structure of GluA2 in the presence of quisqualate. In conclusion, this methodological study may serve as an example for future SANS studies on membrane proteins.


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