Abstract

Simple SummaryMembrane proteins are essential to all forms of life. Millions of membrane proteins are found in the lipid membrane layer that surrounds cells, and in the lipid membrane layers that surround smaller cellular compartments. Many medicines interact with membrane proteins; these include drugs that treat cancer, heart disease and pain. Research into membrane proteins is therefore important to the design and development of new medicines. Membrane proteins are difficult to work with, partly because they are so small. However, using techniques such as X-ray crystallography and electron microscopy, structural biologists, including those at the Membrane Protein Laboratory, are able to see the atomic detail of membrane proteins. There has been great progress in the field of membrane protein structural biology over the past fifteen years. Here, we review the recent advances in membrane protein structural biology, highlight key methods and give an overview of techniques. We also discuss the challenges that remain in this field, and suggest areas for future research.Membrane proteins are essential components of many biochemical processes and are important pharmaceutical targets. Membrane protein structural biology provides the molecular rationale for these biochemical process as well as being a highly useful tool for drug discovery. Unfortunately, membrane protein structural biology is a difficult area of study due to low protein yields and high levels of instability especially when membrane proteins are removed from their native environments. Despite this instability, membrane protein structural biology has made great leaps over the last fifteen years. Today, the landscape is almost unrecognisable. The numbers of available atomic resolution structures have increased 10-fold though advances in crystallography and more recently by cryo-electron microscopy. These advances in structural biology were achieved through the efforts of many researchers around the world as well as initiatives such as the Membrane Protein Laboratory (MPL) at Diamond Light Source. The MPL has helped, provided access to and contributed to advances in protein production, sample preparation and data collection. Together, these advances have enabled higher resolution structures, from less material, at a greater rate, from a more diverse range of membrane protein targets. Despite this success, significant challenges remain. Here, we review the progress made and highlight current and future challenges that will be overcome.

Highlights

  • Membrane proteins (MPs) are located in cellular and organellular membranes as well as the external layers of enveloped viruses

  • The first of these led to the first human structure of a G-protein coupled receptor (GPCR); the β2 adrenergic receptor and the method has been developed into a standardised approach that can be applied to other GPCRs and MPs [85,150]

  • High lipid and detergent concentrations are systematically screened using detergent solubilised samples prior to setting up crystallisation plates via vapour diffusion. This systematic screening has the advantage of stabilising MPs prior to crystallisation and leads to type II crystals which can be harvested

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Summary

Introduction

Membrane proteins (MPs) are located in cellular and organellular membranes as well as the external layers of enveloped viruses. Number membrane protein structures solved eachresonance year by spectroscopy electron diffraction electron microscopy of (EM), X-ray crystallography and nuclear magnetic (ED), electron. The MPL was focused on supporting projects with protein crystals or purified protein that was ready for crystallisation It became apparent from rejected applications and multiple enquiries that there was a need to support researchers who were having difficulties with expressing and purifying MPs. More than 50% of our visiting scientists require assistance with MP production (Figure 1). This review highlights the major technological and methodological developments that have led to improvements in recombinant MP production, sample preparation and advances in data collection. We discuss common issues and highlight methodologies that have been useful to MPL scientists

Recombinant Membrane Protein Production
Generating Constructs for Recombinant Protein Expression
Recombinant Membrane Protein Expression
Fusion Tags and Resins for MP Purification
A SRT-300
Stabilisation of Membrane Proteins for Structural Studies
Use of Encapsulation Agents to Stabilise Membrane Proteins
Genetic Engineering of MPs to Improve Protein Stabilisation
Chaperones and Ligands to Aid MP Stabilisation
Assessing the Quality of Purified MPs
Advances in Sample Preparation and Data Collection
Membrane Protein Crystallisation and Data Collection
Preparation of Membrane Proteins for Cryo-EM and Data Collection
Conclusions and Future Perspectives
Methods
Findings
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