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Plant Pattern Recognition Receptors

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Cover of 'Plant Pattern Recognition Receptors'

Table of Contents

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    Book Overview
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    Chapter 1 Peptidoglycan Isolation and Binding Studies with LysM-Type Pattern Recognition Receptors
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    Chapter 2 Characterization of Plant Cell Wall Damage-Associated Molecular Patterns Regulating Immune Responses
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    Chapter 3 Methods of Isolation and Characterization of Oligogalacturonide Elicitors
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    Chapter 4 Quantitative Analysis of Ligand-Induced Endocytosis of FLAGELLIN-SENSING 2 Using Automated Image Segmentation
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    Chapter 5 Analysis for Protein Glycosylation of Pattern Recognition Receptors in Plants
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    Chapter 6 Assays to Investigate the N-Glycosylation State and Function of Plant Pattern Recognition Receptors
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    Chapter 7 Steady-State and Kinetics-Based Affinity Determination in Effector-Effector Target Interactions
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    Chapter 8 In Vitro Ubiquitination Activity Assays in Plant Immune Responses
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    Chapter 9 Bioinformatics Analysis of the Receptor-Like Kinase (RLK) Superfamily
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    Chapter 10 Identification of MAPK Substrates Using Quantitative Phosphoproteomics
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    Chapter 11 Analysis of PAMP-Triggered ROS Burst in Plant Immunity
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    Chapter 12 MAPK Assays in Arabidopsis MAMP-PRR Signal Transduction
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    Chapter 13 LeEIX2 Interactors’ Analysis and EIX-Mediated Responses Measurement
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    Chapter 14 CDPK Activation in PRR Signaling
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    Chapter 15 Chitin and Stress Induced Protein Kinase Activation
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    Chapter 16 Measuring Callose Deposition, an Indicator of Cell Wall Reinforcement, During Bacterial Infection in Arabidopsis
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    Chapter 17 Quantitative Evaluation of Plant Actin Cytoskeletal Organization During Immune Signaling
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    Chapter 18 Network Reconstitution for Quantitative Subnetwork Interaction Analysis
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    Chapter 19 Stomatal Bioassay to Characterize Bacterial-Stimulated PTI at the Pre-Invasion Phase of Infection
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    Chapter 20 Using Clear Nail Polish to Make Arabidopsis Epidermal Impressions for Measuring the Change of Stomatal Aperture Size in Immune Response
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    Chapter 21 Characterizing the Immune-Eliciting Activity of Putative Microbe-Associated Molecular Patterns in Tomato
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    Chapter 22 Genome-Wide Analysis of Chromatin Accessibility in Arabidopsis Infected with Pseudomonas syringae
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    Chapter 23 Small RNA and mRNA Profiling of Arabidopsis in Response to Phytophthora Infection and PAMP Treatment
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    Chapter 24 Mapping and Cloning of Chemical Induced Mutations by Whole-Genome Sequencing of Bulked Segregants
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    Chapter 25 Rapid Construction of Multiplexed CRISPR-Cas9 Systems for Plant Genome Editing
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    Chapter 26 Chitin-Triggered MAPK Activation and ROS Generation in Rice Suspension-Cultured Cells
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    Chapter 27 Chitin-Induced Responses in the Moss Physcomitrella patens
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    Chapter 28 Methods to Quantify PAMP-Triggered Oxidative Burst, MAP Kinase Phosphorylation, Gene Expression, and Lignification in Brassicas
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    Chapter 29 Effectoromics-Based Identification of Cell Surface Receptors in Potato
Attention for Chapter 1: Peptidoglycan Isolation and Binding Studies with LysM-Type Pattern Recognition Receptors
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Chapter title
Peptidoglycan Isolation and Binding Studies with LysM-Type Pattern Recognition Receptors
Chapter number 1
Book title
Plant Pattern Recognition Receptors
Published in
Methods in molecular biology, February 2017
DOI 10.1007/978-1-4939-6859-6_1
Pubmed ID
Book ISBNs
978-1-4939-6858-9, 978-1-4939-6859-6
Authors

Ute Bertsche, Andrea A. Gust

Editors

Libo Shan, Ping He

Abstract

In the last decade, more and more plant receptors for complex carbohydrate structures have been described. However, studies on receptor binding to glycan ligands are often hampered due to the technical challenge to obtain pure preparations of homogeneous carbohydrate ligands such as bacterial peptidoglycan (PGN) in amounts suitable for studying protein-glycan interactions. Also, most approaches rely on the availability of defined soluble ligands, which in the case of glycans can rarely be synthesized but have to be purified from the respective microorganism. In this chapter, we describe the purification of complex PGN from sources such as gram-positive bacteria, from which PGN isolation is facilitated due to its larger content in their cell wall. Insoluble PGN can subsequently be used in simple carbohydrate pull-down assays to test for interaction with plant proteins. In this respect, lysin motif (LysM)-domain containing proteins are of particular interest. All plant receptors described to date to be involved in the perception of N-Acetylglucosamine-containing ligands (such as PGN or chitin) have been shown to belong to this protein class. Thus, this chapter will also include the production of recombinant LysM proteins to analyze their PGN interaction.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 18%
Researcher 2 12%
Student > Bachelor 2 12%
Unspecified 1 6%
Student > Doctoral Student 1 6%
Other 2 12%
Unknown 6 35%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 24%
Agricultural and Biological Sciences 4 24%
Unspecified 1 6%
Immunology and Microbiology 1 6%
Unknown 7 41%