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Plant Receptor Kinases

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Cover of 'Plant Receptor Kinases'

Table of Contents

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    Book Overview
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    Chapter 1 Expression of Plant Receptor Kinases in E. coli
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    Chapter 2 Expression of Plant Receptor Kinases in Yeast
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    Chapter 3 Expression of Plant Receptor Kinases in Tobacco BY-2 Cells
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    Chapter 4 Cell-Free Synthesis of Plant Receptor Kinases
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    Chapter 5 Purification of Plant Receptor Kinases from Plant Plasma Membranes
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    Chapter 6 Photoaffinity Labeling of Plant Receptor Kinases
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    Chapter 7 Quantitative Detection of Oxidative Burst upon Activation of Plant Receptor Kinases
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    Chapter 8 Extraction and Curation of Gene Models for Plant Receptor Kinases for Phylogenetic Analysis
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    Chapter 9 In Silico Prediction of Ligand-Binding Sites of Plant Receptor Kinases Using Conservation Mapping
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    Chapter 10 Co-immunoprecipitation of Plant Receptor Kinases
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    Chapter 11 Autophosphorylation Assays Using Plant Receptor Kinases Synthesized in Cell-Free Systems
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    Chapter 12 Investigation of Autophosphorylation Sites of Plant Receptor Kinases and Phosphorylation of Interacting Partners
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    Chapter 13 In Vitro Assessment of Guanylyl Cyclase Activity of Plant Receptor Kinases
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    Chapter 14 BiFC Assay to Detect Calmodulin Binding to Plant Receptor Kinases
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    Chapter 15 Pull-down Assay to Characterize Ca 2+ /Calmodulin Binding to Plant Receptor Kinases
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    Chapter 16 The Use of FRET/FLIM to Study Proteins Interacting with Plant Receptor Kinases
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    Chapter 17 Detection and Analyses of Endocytosis of Plant Receptor Kinases
Attention for Chapter 15: Pull-down Assay to Characterize Ca 2+ /Calmodulin Binding to Plant Receptor Kinases
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Chapter title
Pull-down Assay to Characterize Ca 2+ /Calmodulin Binding to Plant Receptor Kinases
Chapter number 15
Book title
Plant Receptor Kinases
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7063-6_15
Pubmed ID
Book ISBNs
978-1-4939-7062-9, 978-1-4939-7063-6
Authors

Christine Kaufmann, Margret Sauter, Kaufmann, Christine, Sauter, Margret

Abstract

Plant receptor-like kinases (RLKs) are regulated by posttranscriptional modification and by interaction with regulatory proteins. A common modification of RLKs is (auto)phosphorylation, and a common regulatory protein is the calcium sensor calmodulin (CaM). We have developed protocols to detect the interaction of an RLK with CaM. The interaction with CaM was shown by bimolecular fluorescence complementation (BiFC) (see Chapter 14) and pull-down assay (this chapter). Both methods offer unique advantages. BiFC is useful in showing interaction of soluble as well as of membrane-bound proteins in planta. Pull-down assays are restricted to soluble proteins and provide in vitro data. The pull-down assay provides the advantage that proteins can be modified prior to binding and that experimental conditions such as the concentration of Ca(2+) or other divalent cations can be controlled. This chapter provides a pull-down protocol to study RLK-CaM interaction with optional steps to investigate the impact of RLK phosphorylation or of Ca(2+).

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 1 11%
Unknown 8 89%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 11%
Researcher 1 11%
Professor 1 11%
Student > Postgraduate 1 11%
Other 1 11%
Other 1 11%
Unknown 3 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 44%
Biochemistry, Genetics and Molecular Biology 1 11%
Unspecified 1 11%
Unknown 3 33%