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Plant Proteomics : Methods and Protocols / edited by Hervé Thiellement, Michel Zivy, Catherine Damerval, Valérie Méchin.

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Holman Biotech Commons QH506 .M45 v.1 (1984)-v.20 (1993),v.22 (1994),v.24 (1994)-v.53 (1996), v.42 (1995) and v.51 (1995) reported missing 3-13-2000 v.55 (1995),v.58 (1996)-v.63 (1997), v.65 (1996)-v.154 (2001), v.156 (2001)-190 (2002), v.192 (2002)-v.407 (2007) v.409 (2007)-v.416 (2008),v.418 (2008)-v.466 v.468-v.490,v.492,v.494,v.496-499 501-506,508,510-512,514,516-517,519-536 538,540-569,571 573-589,591-608,610-615,617,620-627,630-633,636,638,642
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Format:
Book
Contributor:
Thiellement, Hervé, editor.
Zivy, Michel, editor.
Damerval, Catherine, editor.
Méchin, Valérie, editor.
SpringerLink (Online service)
Series:
Methods in molecular biology 1064-3745 ; 355.
Springer Protocols (Springer-12345)
Methods in Molecular Biology, 1064-3745 ; 355
Language:
English
Subjects (All):
Life sciences.
Botany.
Life Sciences.
Plant Sciences.
Local Subjects:
Life Sciences.
Plant Sciences.
Physical Description:
1 online resource (416 pages) : 135 illustrations.
Contained In:
Springer eBooks
Place of Publication:
Totowa, NJ : Humana Press, 2007.
System Details:
text file PDF
Summary:
The aim of Plant Proteomics: Methods and Protocols is to present up-- date methods and protocols used by recognized scientists in the world of plant proteomics. If this world was a very small one twenty-five years ago when the first papers were published, it has since experienced exponential growth, and in most countries around the world there are laboratories working on plant proteomics. Two-dimensional gel electrophoresis is still the basic method used, but it has been improved greatly with IPG in the first dimension (Chapter 13) and with new detection methods with fluorochromes (Chapters 14 and 15). Signi- cant progress has been achieved in protein extraction, which is particularly difficult with plant tissues containing phenols, proteases, and other secondary metabolites that interfere with proteins. Standard procedures have been op- mized (Chapters 1 and 2) for peculiar tissues (Chapters 3, 4, and 5) and cellular compartments (Chapters 6 to 10). These methods rely on improvements made in the solubilization of proteins from membranes (Chapters 11 and 12). Mass spectrometry was a revolution that permitted the high throughput identifi- tion of proteins separated by 2D gels (Chapters 19 and 20) but also from blue native 1D gels (Chapters 27 and 28) despite the fact that Edman sequencing can still be useful (Chapter 18). Associated with other techniques such as 2DLC or LC of intact proteins, mass spectrometry also permits the identification of polypeptides from complexes (Chapters 21 and 22).
Contents:
Total Protein Extraction with TCA-Acetone
Phenol Extraction of Proteins for Proteomic Studies of Recalcitrant Plant Tissues
Protein Extraction from Cereal Seeds
Protein Extraction from Xylem and Phloem Sap
Protein Extraction from Woody Plants
Isolation of Chloroplast Proteins from Arabidopsis thaliana for Proteome Analysis
Isolation and Subfractionation of Plant Mitochondria for Proteomic Analysis
Extraction of Nuclear Proteins from Root Meristematic Cells
Extraction of Nuclear Proteins
Isolation of Cell Wall Proteins from Medicago sativa Stems
Plant Plasma Membrane Protein Extraction and Solubilization for Proteomic Analysis
Detergents and Chaotropes for Protein Solubilization before Two-Dimensional Electrophoresis
Two-Dimensional Electrophoresis for Plant Proteomics
Visible and Fluorescent Staining of Two-Dimensional Gels
Two-Dimensional Differential In-Gel Electrophoresis (DIGE) of Leaf and Roots of Lycopersicon esculentum
Quantitative Analysis of 2D Gels
Multivariate Data Analysis of Proteome Data
Edman Sequencing of Proteins from 2D Gels
Peptide Mass Fingerprinting
Protein Identification Using Nano Liquid Chromatography-Tandem Mass Spectrometry
Two-Dimensional Nanoflow Liquid Chromatography-Tandem Mass Spectrometry of Proteins Extracted from Rice Leaves and Roots
Separation, Identification, and Profiling of Membrane Proteins by GFC/IEC/SDS-PAGE and MALDI TOF MS
The PROTICdb Database for 2-DE Proteomics
Identification of Phosphorylated Proteins
Plant Proteomics and Glycosylation
Blue-Native Gel Electrophoresis for the Characterization of Protein Complexes in Plants
Electroelution of Intact Proteins from SDS-PAGE Gels and Their Subsequent MALDI-TOF MS Analysis
Generation of Plant Protein Microarrays and Investigation of Antigen-Antibody Interactions
Phosphorylation Studies Using Plant Protein Microarrays.
Other Format:
Printed edition:
ISBN:
9781597452274
Access Restriction:
Restricted for use by site license.

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