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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 9: Fractionation Techniques to Examine Effector Translocation.
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Chapter title
Fractionation Techniques to Examine Effector Translocation.
Chapter number 9
Book title
Type 3 Secretion Systems
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6649-3_9
Pubmed ID
Book ISBNs
978-1-4939-6647-9, 978-1-4939-6649-3
Authors

Rachel M. Olson, Deborah M. Anderson

Editors

Matthew L. Nilles, Danielle L. Jessen Condry

Abstract

Many Gram-negative bacterial pathogens use type III secretion systems to export proteins that act directly on the host and aid in the infectious process. Extracellular bacteria primarily rely upon the type III secretion system to insert or inject effector proteins into the cytosol of their host cell in order to perturb intracellular signaling events and aid in pathogenesis. Intracellular bacteria can also depend on the T3SS translocation of effector proteins from vacuolar compartments into the vacuolar membrane or host cell cytosol where they can modulate intracellular trafficking and/or signaling pathways necessary for their growth and survival. Biochemical fractionation of infected cells in vitro enables detection of these events, making it possible to identify relevant protein-protein interactions, characterize phenotypes of mutant strains and understand how these effector proteins impact host cells. In this chapter we provide methods for the analysis of translocated effector proteins using biochemical and mechanical fractionation procedures.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 67%
Student > Doctoral Student 1 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 33%
Agricultural and Biological Sciences 1 33%
Immunology and Microbiology 1 33%