The Protein Protocols Handbook

The third edition of The Protein Protocols Handbook introduces 57 critically important new chapters, and significantly updates the previous edition's tried-and-trusted methods. The book offers over 200 key, readily reproducible protocols that ensure results.

Since the publication of the bestselling second edition of John Walker's widely acclaimed Protein Protocols Handbook, there have been continual methodological developments in the field of protein chemistry. This greatly enhanced third edition introduces 57 critically important new chapters, as well as significantly updating the previous edition's tried-and-true methods. Although the timely new chapters are spread throughout all of the book, the vital section on post-translational modifications has been expanded most to reflect the increasing importance of these modifications in the understanding of protein function.

Each readily reproducible method follows the highly praised format of the Methods in Molecular Biology™ series, offering a concise summary of its basic theory, a complete materials list, a step-by-step protocol for its successful execution, and extensive notes on avoiding pitfalls, or on modifying the method to function within your own experimental circumstances. The expert authors of each chapter have demonstrated a hands-on mastery of the methods described, fine-tuned here for optimal productivity.

Comprehensive, cutting-edge, and highly practical, The Protein Protocols Handbook, Third Edition is today's indispensable benchtop manual and guide, not only for all those new to the protein chemistry laboratory, but also for those established workers seeking to broaden their armamentarium of techniques in the urgent search for rapid and robust results

Offers over 200 key, readily reproducible protocols that ensure robust, successful results Includes many new techniques for the study of post-translational modifications Demonstrates the range of techniques available and their strengths and limitations Contains numerous time-saving techniques for even the most highly skilled researchers

Contenu

Protein Determination by UV Absorption.- The Lowry Method for Protein Quantitation.- The Bicinchoninic Acid (BCA) Assay for Protein Quantitation.- The Bradford Method for Protein Quantitation.- Ultrafast Protein Determinations Using Microwave Enhancement.- The Nitric Acid Methods for Protein Estimation in Biological Samples.- Quantitation of Tryptophan in Proteins.- Kinetic Silver Staining of Proteins.- Quantitation of cellular proteins by flow cytometry.- Quantitation of cellular proteins by laser scanning cytometry.- Protein Solubility in 2D Electrophoresis: Basic principles and issues.- Mouse and Human Tissues Sample Preparation for 2-D Electrophoresis.- Plant Protein sample preparation for 2DE.- Preparation of bacterial samples for 2-D PAGE.- Preparation of bodily fluids for 2-D PAGE.- Immunoaffinity Depletion of high abundance plasma and serum proteins.- Preparation of Yeast samples for 2D PAGE.- Membrane Protein Preparation Using Aqueous Polymer Two Phase Systems.- Subcellular fractionation of small sample amounts.- Nondenaturing Polyacrylamide Gel Electrophoresis of Proteins.- SDS Polyacrylamide Gel Electrophoresis of Proteins.- Gradient SDS Polyacrylamide Gel Electrophoresis of Proteins.- SDS-Polyacrylamide Gel Electrophoresis of Peptides.- Blue native gel electrophoresis (BN-PAGE).- Separation of proteins by gel electrophoresis in the Tris-Taurine-HCl system.- Cetyltrimethylammonium Bromide Discontinuous Gel Electrophoresis of Proteins: M -Based Separation of Proteins with Retained Native Activity.- Acetic Acid-Urea Polyacrylamide Gel Electrophoresis of Basic Proteins.- Acid-Urea-Triton Polyacrylamide Gel Electrophoresis of Histones.- Isoelectric Focusing of Proteins in Ultra-Thin Polyacrylamide Gels.- Serial immobilized pH gradient isoelectric focusing over pH 4-9.- Radiolabelling of Eukaryotic Cells and Subsequent Preparation for 2-D.- Two-Dimensional PAGE Using Carrier Ampholyte pH Gradients in the First Dimension.- Vertical agarose electrophoresis and electroblotting of high molecular weight proteins.- 2D PAGE of high molecular weight proteins.- Casting immobilised pH gradients.- Nonequilibrium pH Gel Electrophoresis.- Microchip capillary electrophoresis.- Protein Separations in Microfluidic Chips.- Difference gel electrophoresis (DIGE).- Comparing 2-D Electrophoresis Gels Across Internet Databases.- Quantification of Radiolabeled Proteins in Polyacrylamide Gels 25.4.07.- Differential ProteoTope radioactive quantification of protein abundance ratios.- Quantitation of Proteins on Polyacrylamide Gels.- Using SDS-PAGE and scanning laser densitometry to measure proteins.- Rapid and Sensitive Staining of Unfixed Proteins in Polyacrylamide Gels with Nile Red.- Zinc reverse staining technique.- Protein Staining with Calconcarboxylic Acid in Polyacrylamide Gels.- Detection of Proteins in Polyacrylamide Gels by Silver Staining.- Background-free Protein Detection on Polyacrylamide Gels and on Electroblots Using Transition Metal Chelate Stains.- Detection of Proteins in Polyacrylamide Gels by Fluorescent Staining.- Detection of Glycoproteins in Gels and Blots.- Staining of Glycoproteins/Proteoglycans on SDS-Gels.- Detection of Proteins and Sialoglycoproteins in Polyacrylamide Gels Using Eosin X stain.- Pro-Q Diamond phosphoprotein staining.- Electroelution of Proteins from Polyacrylamide Gels.- Autoradiography and Fluorography of Acrylamide Gels.- Proteolytic Activity Detection by Two-Dimensional Zymography.- Protein Blotting by Electroblotting.- Protein Blotting by the Semi-dry Method.- Protein Blotting by the Capillary Method.- Western Blotting of basic proteins electrophoretically resolved on acid-urea-Triton-polyacrylamide gels.- Immunoblotting of 2-DE Separated Proteins.- High efficiency blotting of high-molecular weight proteins.- Alkaline Phosphatase Labeling of IgG Antibody.- b-Galactosidase Labeling of IgG Antibody.- Horseradish Peroxidase Labeling of IgG Antibody.- Digoxigenin (DIG) Labelling of IgG Antibody.- Conjugation of fluorochromes to antibodies.- Coupling of Antibodies with Biotin.- Preparation of Avidin Conjugates.- MDPF Staining of Proteins on Western Blots.- Copper Iodided Staining of Proteins and its silver enhancement.- Detection of Proteins on Blots using Direct Blue 71.- Detection of proteins on Western blots using colorimetric and radiometric vusialization of Secondary Ligands.- Identification of Glycoproteins on Nitrocellulose Membranes Using Lectin Blotting.- A Sensitive Method to Quantitatively Detect Total Protein on Membranes after Electrophoretic Transfer Using Avidin- or Streptavidin-Biotin.- Detection and Quantification of Proteins on Immunoblots using Enhanced Chemiluminescence.- Reutilization of Western Blots After Chemiluminescent Detection or Autoradiography.- The use of quantum dot luminescent probes for Western blot analysis.- The use of infrared fluorescent dyes in quantitative immunoblotting.- The use of infrared fluorescent dyes in immunofluorescence microscopy.- Carboxymethylation of Cysteine Using Iodoacetamide/Iodoacetic Acid.- Performic Acid Oxidation.- Succinylation of Protein.- Pyridylethylation of Cysteine Residues.- Side-Chain Selective Chemical Modifications of Proteins.- Nitration of Tyrosines.- Ethoxyformylation of Histidine.- Modification of Arginine Side Chains with p-Hydroxyphenylglyoxal.- Amidination of Carboxyl Groups.- Amidination of Lysine Side Chains.- Modification of tryptophan with 2-Hydroxy-5-Nitrogenzylbromide.- Modification of Sulhydryl Groups with DTNB.- Chemical Cleavage of Proteins at Methionyl-X Peptide Bonds.- Chemical Cleavage of Proteins at Tryptophanyl-X Peptide Bonds.- Chemical Cleavage of Proteins at Aspartyl-X Peptide Bonds.- Chemical Cleavage of Proteins at Cysteinyl-X Peptide Bonds.- Chemical Cleavage of Proteins at Asparaginyl-Glycyl Peptide Bonds.- Enzymatic Digestion of Prot…