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Shotgun Proteomics

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Cover of 'Shotgun Proteomics'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Survey of shotgun proteomics.
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    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.
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    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.
  30. Altmetric Badge
    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 31: Top-down proteomics by means of orbitrap mass spectrometry.
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Chapter title
Top-down proteomics by means of orbitrap mass spectrometry.
Chapter number 31
Book title
Shotgun Proteomics
Published in
Methods in molecular biology, April 2014
DOI 10.1007/978-1-4939-0685-7_31
Pubmed ID
Book ISBNs
978-1-4939-0684-0, 978-1-4939-0685-7
Authors

Kai Scheffler, Scheffler, Kai

Editors

Daniel Martins-de-Souza

Abstract

Top-down proteomics has become a popular approach for the analysis of intact proteins. The term "top down" has been coined for the analysis of proteins not involving any enzymatic or chemical cleavage but rather the ionization of the protein as a sound molecule and mass analysis of intact species and fragment ions thereof produced upon dissociation inside a mass spectrometer. One or several charge states of the protein are mass-isolated and subjected to dissociation (MS/MS) in the gas phase. The obtained fragment masses, predominantly from cleavages of the protein along its amino acid backbone, are directly related to the intact protein. Using bioinformatics tools the fragment masses are matched against a known protein sequence or can alternatively be used for partial or full de novo sequencing, depending on the size of the protein and the number of fragment ions obtained. Moreover, this approach provides global information about modification states of proteins including the number and types of isoforms and their stoichiometry and allows for the precise localization of modifications within the amino acid sequence. Top-down analysis of a single, purified protein can be performed by matrix-assisted laser desorption ionization or electrospray ionization upon direct infusion without online chromatographic separation, whereas top-down analysis of complex protein mixtures makes pre-fractionation combined with an efficient front-end chromatographic separation coupled online to the mass spectrometer inevitable.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 20%
Researcher 4 20%
Professor > Associate Professor 3 15%
Student > Bachelor 3 15%
Professor 2 10%
Other 2 10%
Unknown 2 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 40%
Chemistry 4 20%
Agricultural and Biological Sciences 4 20%
Unspecified 1 5%
Unknown 3 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 01 January 2015.
All research outputs
#17,723,043
of 22,758,248 outputs
Outputs from Methods in molecular biology
#7,188
of 13,089 outputs
Outputs of similar age
#156,120
of 226,077 outputs
Outputs of similar age from Methods in molecular biology
#50
of 153 outputs
Altmetric has tracked 22,758,248 research outputs across all sources so far. This one is in the 19th percentile – i.e., 19% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,089 research outputs from this source. They receive a mean Attention Score of 3.3. This one is in the 39th percentile – i.e., 39% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 226,077 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 27th percentile – i.e., 27% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 153 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 64% of its contemporaries.