Biophysicists find a way to take a peek at how membrane receptors work

Biophysicists find a way to take a peek at how membrane receptors work
General appearance of the G protein-coupled receptor. Credit: Anastasia Gusach et al./Current Opinion in Structural Biology

In a study published in Current Opinion in Structural Biology, MIPT biophysicists explained ways to visualize membrane receptors in their different states. Detailed information on the structure and dynamics of these proteins will enable developing effective and safe drugs to treat many sorts of conditions.

Every second, living cells receive myriads of signals from their environment, which are usually transmitted through dedicated signaling molecules such as hormones. Most of these molecules are incapable of penetrating the cell membrane so for the most part, such signals are identified at the membrane. For that purpose, the is equipped with .

These receive outside signals and 'interpret' them into the language the cell can understand. Cell surface receptors are vital for proper functioning of cells and the organism as a whole. Should the receptors stop working as intended, the communication between becomes disrupted, which can lead to the organism developing a medical condition.

GPCRs (G protein-coupled receptors) are a large family of membrane receptors that share a common structure; they all have seven protein spirals that cross the membrane and couple the receptor to a G protein situated on the inside of the cell. Interaction of the signal molecule with the receptor triggers a change in the 3-D structure, or conformation, of the receptor, which activates the G protein. The activated G protein, in turn, triggers a signal cascade inside the cell, which results in a response to the signal.

Biophysicists find a way to take a peek at how membrane receptors work
Key GPCR family receptors that are related to diseases. Credit: Anastasia Gusach et al./Current Opinion in Structural Biology

GPCR family membrane proteins have been linked to a lot of neurodegenerative and cardiovascular diseases and certain types of cancer. GPCR proteins have also been proven to contribute to conditions such as obesity, diabetes, mental disorders, and others. As a result, GPCRs have become a popular drug target, with a large number of drugs currently on the market targeting this particular family of receptors.

One of the modern approaches to drug development involves analyzing 3-D structures of GPCR molecules. But membrane receptor analysis is a slow and extremely laborious process and even when successful, it does not completely reveal the molecule's behavior inside the cell.

"Currently, scientists have two options when it comes to studying proteins. They can either 'freeze' a protein and have its precise static snapshot, or study its dynamics at the cost of losing details. The former approach uses methods such as crystallography and ; the latter uses spectroscopic techniques," comments Anastasia Gusach, a research fellow at the MIPT Laboratory of Structural Biology of G-protein Coupled Receptors.

The authors of the study demonstrated how combining both the structural and the spectroscopic approaches result in "the best of both worlds" in terms of obtaining precise information on functioning of GPCRs. For instance, the double electron-electron resonance (DEER) and the Förster resonance energy transfer (FRET) techniques act as an "atomic ruler," ensuring precise measurements of distances between separate atoms and their groups within the protein. The nuclear magnetic resonance method enables visualizing the overall shape of the receptor molecule while modified mass spectrometry methods (MRF-MS, HDX-MS) help trace the susceptibility of separate groups of atoms constituting the protein to the solvent, thus indicating which parts of the molecule face outwards.

Biophysicists find a way to take a peek at how membrane receptors work
Sequence of processes triggered by activation of an GPCR receptor. Credit: Anastasia Gusach et al./Current Opinion in Structural Biology

"Studying the GPCR dynamics uses cutting-edge methods of experimental biophysical analysis such as nuclear magnetic resonance (NMR) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, and advanced fluorescence microscopy techniques including single-molecule microscopy," says Alexey Mishin, deputy head of the MIPT Laboratory for Structural Biology of G- Coupled Receptors.

"Biophysicists that use different methods to study GPCRs have been widely organizing collaborations that already bore some fruitful results. We hope that this review will help scientists specializing in different methods to find some new common ground and work together to obtain a better understanding of receptors' functioning," adds Anastasia Gusach.

The precise information on how the receptors function and transfer between states will greatly expand the capabilities for structure-based drug design.


Explore further

A new accurate computational method designed to enhance drug target stability

More information: Anastasia Gusach et al, Beyond structure: emerging approaches to study GPCR dynamics, Current Opinion in Structural Biology (2020). DOI: 10.1016/j.sbi.2020.03.004
Citation: Biophysicists find a way to take a peek at how membrane receptors work (2020, May 21) retrieved 31 May 2020 from https://phys.org/news/2020-05-biophysicists-peek-membrane-receptors.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
8 shares

Feedback to editors

User comments