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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 7: Assessing Extracellular ATP as Danger Signal In Vivo: The pmeLuc System.
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Chapter title
Assessing Extracellular ATP as Danger Signal In Vivo: The pmeLuc System.
Chapter number 7
Book title
NLR Proteins
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3566-6_7
Pubmed ID
Book ISBNs
978-1-4939-3564-2, 978-1-4939-3566-6
Authors

Francesco Di Virgilio, Paolo Pinton, Simonetta Falzoni

Editors

Francesco Di Virgilio, Pablo Pelegrín

Abstract

Inflammation is the key pathophysiological response triggered by noxious agents in multicellular organisms. Central to inflammation is detection of exogenous or endogenous danger signals by immune cells. Extracellular ATP is a ubiquitous danger signal released during septic or sterile inflammation. The development of reliable techniques to measure extracellular ATP in vivo has become an urgent need in inflammation studies after the discovery that the most potent plasma membrane receptor responsible for NLRP3 inflammasome activation is an ATP-activated receptor, P2RX7. Here we describe an easy bioluminescence technique for the measurement of extracellular ATP in vivo.

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Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 21 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 24%
Student > Bachelor 3 14%
Student > Doctoral Student 2 10%
Professor 1 5%
Other 1 5%
Other 2 10%
Unknown 7 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 24%
Immunology and Microbiology 3 14%
Medicine and Dentistry 3 14%
Materials Science 1 5%
Unknown 9 43%