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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 10: Measurement of Effector Protein Translocation Using Phosphorylatable Epitope Tags and Phospho-Specific Antibodies.
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Chapter title
Measurement of Effector Protein Translocation Using Phosphorylatable Epitope Tags and Phospho-Specific Antibodies.
Chapter number 10
Book title
Type 3 Secretion Systems
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6649-3_10
Pubmed ID
Book ISBNs
978-1-4939-6647-9, 978-1-4939-6649-3
Authors

Sara Schesser Bartra, Gregory V. Plano

Editors

Matthew L. Nilles, Danielle L. Jessen Condry

Abstract

Numerous bacterial pathogens employ specialized protein secretion machineries to directly inject anti-host proteins, termed effector proteins, into eukaryotic cells. Effector proteins carrying small phosphorylatable tags can be used to detect and quantify effector protein injection. Here, we describe the use of the ELK- and GSK-tags to detect the translocation of the Y. pestis YopE effector protein into RAW 264.7 macrophage-like cells using immunoblot analysis with phospho-specific antibodies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 38%
Unspecified 1 13%
Librarian 1 13%
Professor 1 13%
Unknown 2 25%
Readers by discipline Count As %
Immunology and Microbiology 2 25%
Biochemistry, Genetics and Molecular Biology 1 13%
Unspecified 1 13%
Computer Science 1 13%
Nursing and Health Professions 1 13%
Other 0 0%
Unknown 2 25%