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Type 3 Secretion Systems

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Cover of 'Type 3 Secretion Systems'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction to Type III Secretion Systems.
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    Chapter 2 Site-Directed Mutagenesis and Its Application in Studying the Interactions of T3S Components.
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    Chapter 3 Blue Native Protein Electrophoresis to Study the T3S System Using Yersinia pestis as a Model.
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    Chapter 4 In Vivo Photo-Cross-Linking to Study T3S Interactions Demonstrated Using the Yersinia pestis T3S System.
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    Chapter 5 Isolation of Type III Secretion System Needle Complexes by Shearing.
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    Chapter 6 Use of Transcriptional Control to Increase Secretion of Heterologous Proteins in T3S Systems.
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    Chapter 7 Characterization of Type Three Secretion System Translocator Interactions with Phospholipid Membranes.
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    Chapter 8 Analysis of Type III Secretion System Secreted Proteins.
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    Chapter 9 Fractionation Techniques to Examine Effector Translocation.
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    Chapter 10 Measurement of Effector Protein Translocation Using Phosphorylatable Epitope Tags and Phospho-Specific Antibodies.
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    Chapter 11 A TAL-Based Reporter Assay for Monitoring Type III-Dependent Protein Translocation in Xanthomonas.
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    Chapter 12 Subcellular Localization of Pseudomonas syringae pv. tomato Effector Proteins in Plants.
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    Chapter 13 A Method for Characterizing the Type III Secretion System's Contribution to Pathogenesis: Homologous Recombination to Generate Yersinia pestis Type III Secretion System Mutants.
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    Chapter 14 Detecting Immune Responses to Type III Secretion Systems.
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    Chapter 15 Recombinant Expression and Purification of the Shigella Translocator IpaB.
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    Chapter 16 Expression and Purification of N-Terminally His-Tagged Recombinant Type III Secretion Proteins.
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    Chapter 17 Mouse Immunization with Purified Needle Proteins from Type III Secretion Systems and the Characterization of the Immune Response to These Proteins.
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    Chapter 18 Identification of the Targets of Type III Secretion System Inhibitors.
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    Chapter 19 Detection of Protein Interactions in T3S Systems Using Yeast Two-Hybrid Analysis.
Attention for Chapter 19: Detection of Protein Interactions in T3S Systems Using Yeast Two-Hybrid Analysis.
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Chapter title
Detection of Protein Interactions in T3S Systems Using Yeast Two-Hybrid Analysis.
Chapter number 19
Book title
Type 3 Secretion Systems
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6649-3_19
Pubmed ID
Book ISBNs
978-1-4939-6647-9, 978-1-4939-6649-3
Authors

Matthew L. Nilles

Editors

Matthew L. Nilles, Danielle L. Jessen Condry

Abstract

Two-hybrid systems, sometimes termed interaction traps, are genetic systems designed to find and analyze interactions between proteins. The most common systems are yeast based (commonly Saccharomyces cerevisae) and rely on the functional reconstitution of the GAL4 transcriptional activator. Reporter genes, such as the lacZ gene of Escherichia coli (encodes β-galactosidase), are placed under GAL4-dependent transcriptional control to provide quick and reliable detection of protein interactions. In this method the use of a yeast-based two-hybrid system is described to study protein interactions between components of type III secretion systems.

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Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 1 100%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 100%