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Shotgun Proteomics

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Cover of 'Shotgun Proteomics'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Survey of shotgun proteomics.
  3. Altmetric Badge
    Chapter 2 LC-MALDI-TOF/TOF for Shotgun Proteomics.
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    Chapter 3 Fully automatable multidimensional reversed-phase liquid chromatography with online tandem mass spectrometry.
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    Chapter 4 GeLC-MS/MS Analysis of Complex Protein Mixtures.
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    Chapter 5 IPG Strip-Based Peptide Fractionation for Shotgun Proteomics.
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    Chapter 6 SILAC Yeast: From Labeling to Comprehensive Proteome Quantification.
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    Chapter 7 Analysis of proteome dynamics in mice by isotopic labeling.
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    Chapter 8 Stable Isotope Labeling in Mammals (SILAM).
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    Chapter 9 Analysis of individual protein turnover in live animals on a proteome-wide scale.
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    Chapter 10 Determining Protein Subcellular Localization in Mammalian Cell Culture with Biochemical Fractionation and iTRAQ 8-Plex Quantification.
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    Chapter 11 Brain Quantitative Proteomics Combining GeLC-MS and Isotope-Coded Protein Labeling (ICPL)
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    Chapter 12 Employing TMT Quantification in a Shotgun-MS Platform.
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    Chapter 13 Employing TMT Quantification in Shotgun-MS Proteomic Analysis: A Focus on Skeletal Muscle.
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    Chapter 14 Spectral counting label-free proteomics.
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    Chapter 15 Quantification of Proteins by Label-Free LC-MS(E.).
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    Chapter 16 Bioinformatics for proteomics: opportunities at the interface between the scientists, their experiments, and the community.
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    Chapter 17 Identification of DNA Damage Checkpoint-Dependent Protein Interactions in Saccharomyces cerevisiae Using Quantitative Mass Spectrometry.
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    Chapter 18 Application of shotgun proteomics for discovery-driven protein-protein interaction.
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    Chapter 19 Mapping protein complexes using covalently linked antibodies and isobaric mass tags.
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    Chapter 20 Biomarker verification using selected reaction monitoring and shotgun proteomics.
  22. Altmetric Badge
    Chapter 21 Use of Universal Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC)-Based Selected Reaction Monitoring (SRM) Approach for Verification of Breast Cancer-Related Protein Markers.
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    Chapter 22 The Secretome Analysis by High-Throughput Proteomics and Multiple Reaction Monitoring (MRM).
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    Chapter 23 Preparation of heteroelement-incorporated and stable isotope-labeled protein standards for quantitative proteomics.
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    Chapter 24 One-source peptide/phosphopeptide ratio standards for accurate and site-specific determination of the degree of phosphorylation.
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    Chapter 25 Quantitative glycoproteomics for N-glycoproteome profiling.
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    Chapter 26 A practical recipe to survey phosphoproteomes.
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    Chapter 27 Quantitation of the Phosphoproteome Using the Library-Assisted eXtracted Ion Chromatogram (LAXIC) Strategy.
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    Chapter 28 Fast, efficient, and quality-controlled phosphopeptide enrichment from minute sample amounts using titanium dioxide.
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    Chapter 29 Quantifying small molecule-induced changes in cellular protein expression and posttranslational modifications using isobaric mass tags.
  31. Altmetric Badge
    Chapter 30 Analysis of protein structure by cross-linking combined with mass spectrometry.
  32. Altmetric Badge
    Chapter 31 Top-down proteomics by means of orbitrap mass spectrometry.
Attention for Chapter 2: LC-MALDI-TOF/TOF for Shotgun Proteomics.
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Chapter title
LC-MALDI-TOF/TOF for Shotgun Proteomics.
Chapter number 2
Book title
Shotgun Proteomics
Published in
Methods in molecular biology, April 2014
DOI 10.1007/978-1-4939-0685-7_2
Pubmed ID
Book ISBNs
978-1-4939-0684-0, 978-1-4939-0685-7
Authors

Fernández-Puente P, Mateos J, Blanco FJ, Ruiz-Romero C, Patricia Fernández-Puente, Jesús Mateos, Francisco J. Blanco M.D., Cristina Ruiz-Romero, Fernández-Puente, Patricia, Mateos, Jesús, Blanco, Francisco J., Ruiz-Romero, Cristina, Francisco J. Blanco

Editors

Daniel Martins-de-Souza

Abstract

Automated liquid chromatography tandem mass spectrometry (LC-MS/MS) is a well-established technique for identification of components from complex mixtures in shotgun proteomics experiments. Approaches involving the use of matrix-assisted laser desorption/ionization mass spectrometry (LC-MALDI-MS/MS) comprise the preparation of protein extracts, their enzymatic digestion, the separation of the resulting peptides by nanoscale liquid chromatography coupled to a collector that deposits the microfractions onto a MALDI plate, and finally the mass spectrometry analysis of the fractions. Using an LC-MALDI strategy, the rate of the collection of MS/MS data is decoupled from the chromatographic separation, thus allowing high-quality data which are often complementary to electrospray ionization (LC-ESI-MS/MS) techniques.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 5%
Unknown 20 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 19%
Other 2 10%
Researcher 2 10%
Lecturer > Senior Lecturer 1 5%
Lecturer 1 5%
Other 4 19%
Unknown 7 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 24%
Agricultural and Biological Sciences 2 10%
Unspecified 1 5%
Veterinary Science and Veterinary Medicine 1 5%
Mathematics 1 5%
Other 3 14%
Unknown 8 38%
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Attention Score in Context

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