scholarly journals A rapid expression and purification condition screening protocol for membrane protein structural biology

2017 ◽  
Vol 26 (8) ◽  
pp. 1653-1666 ◽  
Author(s):  
Dan Sjöstrand ◽  
Riccardo Diamanti ◽  
Camilla A. K. Lundgren ◽  
Benjamin Wiseman ◽  
Martin Högbom
Author(s):  
Thi Kim Hoang Trinh ◽  
Weihua Qiu ◽  
Meg Thornton ◽  
Everett E. Carpenter ◽  
Youzhong Guo

2008 ◽  
Vol 130 (23) ◽  
pp. 7357-7363 ◽  
Author(s):  
Qinghai Zhang ◽  
Reto Horst ◽  
Michael Geralt ◽  
Xingquan Ma ◽  
Wen-Xu Hong ◽  
...  

2021 ◽  
Vol 28 ◽  
Author(s):  
Chen-Yan china Zhang ◽  
Shi-Qi Zhao ◽  
Shi-Long Zhang ◽  
Li-Heng Luo ◽  
Ding-Chang Liu ◽  
...  

: Membrane proteins are crucial for biological processes, and many of them are important to drug targets. Understanding the three-dimensional structures of membrane proteins are essential to evaluate their bio function and drug design. High-purity membrane proteins are important for structural determination. Membrane proteins have low yields and are difficult to purify because they tend to aggregate. We summarized membrane protein expression systems, vectors, tags, and detergents, which have deposited in the Protein Data Bank (PDB) in recent four-and-a-half years. Escherichia coli is the most expression system for membrane proteins, and HEK293 cells are the most commonly cell lines for human membrane protein expression. The most frequently vectors are pFastBac1 for alpha-helical membrane proteins, pET28a for beta-barrel membrane proteins, and pTRC99a for monotopic membrane proteins. The most used tag for membrane proteins is the 6×His-tag. FLAG commonly used for alpha-helical membrane proteins, Strep and GST for beta-barrel and monotopic membrane proteins, respectively. The detergents and their concentrations used for alpha-helical, beta-barrel, and monotopic membrane proteins are different, and DDM is commonly used for membrane protein purification. It can guide the expression and purification of membrane proteins, thus contributing to their structure and bio function studying.


2015 ◽  
Vol 33 ◽  
pp. 115-125 ◽  
Author(s):  
Richard Neutze ◽  
Gisela Brändén ◽  
Gebhard FX Schertler

Biology ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 401
Author(s):  
James Birch ◽  
Harish Cheruvara ◽  
Nadisha Gamage ◽  
Peter J. Harrison ◽  
Ryan Lithgo ◽  
...  

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.


Methods ◽  
2011 ◽  
Vol 55 (4) ◽  
pp. 318-323 ◽  
Author(s):  
Qinghai Zhang ◽  
Houchao Tao ◽  
Wen-Xu Hong

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