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Plant Proteostasis

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Cover of 'Plant Proteostasis'

Table of Contents

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    Book Overview
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    Chapter 1 Approaches to Determine Protein Ubiquitination Residue Types
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    Chapter 2 Immunoprecipitation of Cullin-RING Ligases (CRLs) in Arabidopsis thaliana Seedlings
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    Chapter 3 Radioligand Binding Assays for Determining Dissociation Constants of Phytohormone Receptors
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    Chapter 4 Measuring the Enzyme Activity of Arabidopsis Deubiquitylating Enzymes
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    Chapter 5 Fluorescent Reporters for Ubiquitin-Dependent Proteolysis in Plants
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    Chapter 6 Generation of Artificial N-end Rule Substrate Proteins In Vivo and In Vitro
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    Chapter 7 Plant Proteostasis
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    Chapter 8 Plant Proteostasis
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    Chapter 9 Kinetic Analysis of Plant SUMO Conjugation Machinery
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    Chapter 10 Expression, Purification, and Enzymatic Analysis of Plant SUMO Proteases
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    Chapter 11 Quantitative Analysis of Subcellular Distribution of the SUMO Conjugation System by Confocal Microscopy Imaging
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    Chapter 12 Plant Proteostasis
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    Chapter 13 Plant Proteostasis
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    Chapter 14 Protocols for Studying Protein Stability in an Arabidopsis Protoplast Transient Expression System
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    Chapter 15 Detection and Quantification of Protein Aggregates in Plants.
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    Chapter 16 Determination of Protein Carbonylation and Proteasome Activity in Seeds
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    Chapter 17 Isobaric Tag for Relative and Absolute Quantitation (iTRAQ)-Based Protein Profiling in Plants
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    Chapter 18 Plant Proteostasis
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    Chapter 19 In Vivo Radiolabeling of Arabidopsis Chloroplast Proteins and Separation of Thylakoid Membrane Complexes by Blue Native PAGE
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    Chapter 20 Normalized Quantitative Western Blotting Based on Standardized Fluorescent Labeling
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    Chapter 21 Sequence Search and Comparative Genomic Analysis of SUMO-Activating Enzymes Using CoGe
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    Chapter 22 Plant Proteostasis
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    Chapter 23 Bioinformatics Tools for Exploring the SUMO Gene Network
Attention for Chapter 16: Determination of Protein Carbonylation and Proteasome Activity in Seeds
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Chapter title
Determination of Protein Carbonylation and Proteasome Activity in Seeds
Chapter number 16
Book title
Plant Proteostasis
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3759-2_16
Pubmed ID
Book ISBNs
978-1-4939-3757-8, 978-1-4939-3759-2
Authors

Qiong Xia, Hayat El-Maarouf-Bouteau, Christophe Bailly, Patrice Meimoun

Editors

L. Maria Lois, Rune Matthiesen

Abstract

Reactive oxygen species (ROS) have been shown to be toxic but also function as signaling molecules in a process called redox signaling. In seeds, ROS are produced at different developmental stages including dormancy release and germination. Main targets of oxidation events by ROS in cell are lipids, nucleic acids, and proteins. Protein oxidation has various effects on their function, stability, location, and degradation. Carbonylation represents an irreversible and unrepairable modification that can lead to protein degradation through the action of the 20S proteasome. Here, we present techniques which allow the quantification of protein carbonyls in complex protein samples after derivatization by 2,4-dinitrophenylhydrazine (DNPH) and the determination proteasome activity by an activity-based protein profiling (ABPP) using the probe MV151. These techniques, routinely easy to handle, allow the rapid assessment of protein carbonyls and proteasome activity in seeds in various physiological conditions where ROS may act as signaling or toxic elements.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 23%
Other 2 15%
Student > Master 2 15%
Student > Ph. D. Student 1 8%
Unspecified 1 8%
Other 2 15%
Unknown 2 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 31%
Biochemistry, Genetics and Molecular Biology 4 31%
Unspecified 1 8%
Unknown 4 31%