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NLR Proteins

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Cover of 'NLR Proteins'

Table of Contents

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    Book Overview
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    Chapter 1 NLR Proteins
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    Chapter 2 Atypical Inflammasomes.
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    Chapter 3 NLR Proteins
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    Chapter 4 Investigating IL-1β Secretion Using Real-Time Single-Cell Imaging.
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    Chapter 5 NLR Proteins
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    Chapter 6 Measuring IL-1β Processing by Bioluminescence Sensors II: The iGLuc System.
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    Chapter 7 Assessing Extracellular ATP as Danger Signal In Vivo: The pmeLuc System.
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    Chapter 8 Measuring NLR Oligomerization I: Size Exclusion Chromatography, Co-immunoprecipitation, and Cross-Linking.
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    Chapter 9 NLR Proteins
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    Chapter 10 NLR Proteins
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    Chapter 11 Measuring NLR Oligomerization IV: Using Förster Resonance Energy Transfer (FRET)-Fluorescence Lifetime Imaging Microscopy (FLIM) to Determine the Close Proximity of Inflammasome Components.
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    Chapter 12 Measuring NLR Oligomerization V: In Situ Proximity Ligation Assay.
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    Chapter 13 Assessing Caspase-1 Activation.
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    Chapter 14 Cell-Free Assay for Inflammasome Activation.
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    Chapter 15 Functional Reconstruction of NLRs in HEK293 Cells.
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    Chapter 16 Method to Measure Ubiquitination of NLRs.
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    Chapter 17 Cytofluorometric Quantification of Cell Death Elicited by NLR Proteins.
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    Chapter 18 NLR in Human Diseases: Role and Laboratory Findings.
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    Chapter 19 Erratum to: Measuring NLR Oligomerization II: Detection of ASC Speck Formation by Confocal Microscopy and Immunofluorescence
Attention for Chapter 13: Assessing Caspase-1 Activation.
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Chapter title
Assessing Caspase-1 Activation.
Chapter number 13
Book title
NLR Proteins
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3566-6_13
Pubmed ID
Book ISBNs
978-1-4939-3564-2, 978-1-4939-3566-6
Authors

Baptiste Guey, Virginie Petrilli

Editors

Francesco Di Virgilio, Pablo Pelegrín

Abstract

The caspase-1 enzymatic activity plays a major role in the innate immune response as it regulates the maturation of two major proinflammatory cytokines, the interleukin-1beta (IL-1β) and IL-18. In this chapter, we describe the technique of Western blot to assess caspase-1 activation. This method provides multiple information within one experiment. It allows the detection of both unprocessed and processed caspase-1 and substrates.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 17%
Unknown 5 83%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 33%
Student > Bachelor 1 17%
Student > Master 1 17%
Unknown 2 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 33%
Immunology and Microbiology 1 17%
Medicine and Dentistry 1 17%
Unknown 2 33%