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High Throughput Protein Expression and Purification

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Cover of 'High Throughput Protein Expression and Purification'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 High-Throughput Protein Production (HTPP): A Review of Enabling Technologies to Expedite Protein Production
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    Chapter 2 Designing Experiments for High-Throughput Protein Expression
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    Chapter 3 Gateway cloning for protein expression.
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    Chapter 4 Flexi Vector Cloning
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    Chapter 5 The Precise Engineering of Expression Vectors Using High-Throughput In-Fusion™ PCR Cloning
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    Chapter 6 The Polymerase Incomplete Primer Extension (PIPE) method applied to high-throughput cloning and site-directed mutagenesis.
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    Chapter 7 A Family of LIC Vectors for High-Throughput Cloning and Purification of Proteins
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    Chapter 8 “System 48” High-Throughput Cloning and Protein Expression Analysis
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    Chapter 9 Automated 96-Well Purification of Hexahistidine-Tagged Recombinant Proteins on MagneHis Ni 2 +-Particles
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    Chapter 10 E. coli and Insect Cell Expression, Automated Purification and Quantitative Analysis
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    Chapter 11 Hexahistidine-tagged maltose-binding protein as a fusion partner for the production of soluble recombinant proteins in Escherichia coli.
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    Chapter 12 PHB-Intein-Mediated Protein Purification Strategy
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    Chapter 13 High-throughput biotinylation of proteins.
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    Chapter 14 High-Throughput Insect Cell Protein Expression Applications
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    Chapter 15 High-Throughput Protein Expression Using Cell-Free System
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    Chapter 16 The Production of Glycoproteins by Transient Expression in Mammalian Cells
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    Chapter 17 High-Throughput Expression and Detergent Screening of Integral Membrane Proteins
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    Chapter 18 Cell-Free Expression for Nanolipoprotein Particles: Building a High-Throughput Membrane Protein Solubility Platform
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    Chapter 19 Expression and purification of soluble His(6)-tagged TEV protease.
  21. Altmetric Badge
    Chapter 20 High-Throughput Protein Concentration and Buffer Exchange: Comparison of Ultrafiltration and Ammonium Sulfate Precipitation
Attention for Chapter 19: Expression and purification of soluble His(6)-tagged TEV protease.
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Chapter title
Expression and purification of soluble His(6)-tagged TEV protease.
Chapter number 19
Book title
High Throughput Protein Expression and Purification
Published in
Methods in molecular biology, January 2009
DOI 10.1007/978-1-59745-196-3_19
Pubmed ID
Book ISBNs
978-1-58829-879-9, 978-1-59745-196-3
Authors

Tropea, Joseph E, Cherry, Scott, Waugh, David S, Joseph E. Tropea, Scott Cherry, David S. Waugh

Abstract

This chapter describes a simple method for overproducing a soluble form of the tobacco etch virus (TEV) protease in Escherichia coli and purifying it to homogeneity so that it may be used as a reagent for removing affinity tags from recombinant proteins by site-specific endoproteolysis. The protease is initially produced as a fusion to the C-terminus of E. coli maltose binding protein (MBP), which causes it to accumulate in a soluble and active form rather than in inclusion bodies. The fusion protein subsequently cleaves itself in vivo to remove the MBP moiety, yielding a soluble TEV protease catalytic domain with an N-terminal polyhistidine tag. The His-tagged TEV protease can be purified in two steps using immobilized metal affinity chromatography (IMAC) followed by gel filtration. An S219V mutation in the protease reduces its rate of autolysis by approximately 100-fold and also gives rise to an enzyme with greater catalytic efficiency than the wild-type protease.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 390 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 6 2%
Switzerland 1 <1%
Austria 1 <1%
Canada 1 <1%
United Kingdom 1 <1%
Japan 1 <1%
Russia 1 <1%
Unknown 378 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 95 24%
Student > Bachelor 67 17%
Researcher 57 15%
Student > Master 38 10%
Student > Postgraduate 16 4%
Other 57 15%
Unknown 60 15%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 129 33%
Agricultural and Biological Sciences 113 29%
Chemistry 41 11%
Medicine and Dentistry 6 2%
Immunology and Microbiology 4 1%
Other 22 6%
Unknown 75 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 June 2019.
All research outputs
#18,444,553
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Outputs from Methods in molecular biology
#7,923
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Outputs of similar age
#157,883
of 169,377 outputs
Outputs of similar age from Methods in molecular biology
#142
of 163 outputs
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