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Protein Terminal Profiling

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Cover of 'Protein Terminal Profiling'

Table of Contents

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    Book Overview
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    Chapter 1 [14C]-Acetyl-Coenzyme A-Based In Vitro N-Terminal Acetylation Assay
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    Chapter 2 DTNB-Based Quantification of In Vitro Enzymatic N-Terminal Acetyltransferase Activity
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    Chapter 3 SILProNAQ: A Convenient Approach for Proteome-Wide Analysis of Protein N-Termini and N-Terminal Acetylation Quantitation
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    Chapter 4 Profiling of Protein N-Termini and Their Modifications in Complex Samples
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    Chapter 5 Protease Substrate Profiling by N-Terminal COFRADIC
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    Chapter 6 Doublet N-Terminal Oriented Proteomics for N-Terminomics and Proteolytic Processing Identification
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    Chapter 7 Multidimensional Analysis of Protease Substrates and Their Cellular Origins in Mixed Secretomes from Multiple Cell Types
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    Chapter 8 System-Wide Profiling of Protein Amino Termini from Formalin-Fixed, Paraffin-Embedded Tissue Specimens for the Identification of Novel Substrates
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    Chapter 9 Identification of Carboxypeptidase Substrates by C-Terminal COFRADIC
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    Chapter 10 ProC-TEL: Profiling of Protein C-Termini by Enzymatic Labeling
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    Chapter 11 Determining Protease Substrates Within a Complex Protein Background Using the PROtein TOpography and Migration Analysis Platform (PROTOMAP)
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    Chapter 12 Multiplexed Protease Specificity Profiling Using Isobaric Labeling
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    Chapter 13 FPPS: Fast Profiling of Protease Specificity
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    Chapter 14 Profiling of Protease Cleavage Sites by Proteome-Derived Peptide Libraries and Quantitative Proteomics
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    Chapter 15 Prediction of Proteases Involved in Peptide Generation
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    Chapter 16 Live-Cell Imaging of Protease Activity: Assays to Screen Therapeutic Approaches
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    Chapter 17 Protein Translocation Assays to Probe Protease Function and Screen for Inhibitors
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    Chapter 18 Simultaneous Detection of Metalloprotease Activities in Complex Biological Samples Using the PrAMA (Proteolytic Activity Matrix Assay) Method
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    Chapter 19 Synthesis and Application of Activity-Based Probes for Proteases
Attention for Chapter 11: Determining Protease Substrates Within a Complex Protein Background Using the PROtein TOpography and Migration Analysis Platform (PROTOMAP)
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Chapter title
Determining Protease Substrates Within a Complex Protein Background Using the PROtein TOpography and Migration Analysis Platform (PROTOMAP)
Chapter number 11
Book title
Protein Terminal Profiling
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6850-3_11
Pubmed ID
Book ISBNs
978-1-4939-6849-7, 978-1-4939-6850-3
Authors

R. A. Fuhrman-Luck, L. M. Silva, M. L. Hastie, J. J. Gorman, J. A. Clements

Editors

Oliver Schilling

Abstract

The PROtein TOpography and Migration Analysis Platform (PROTOMAP) approach is a degradomics technique used to determine protease substrates within complex protein backgrounds. The method involves protein separation according to protein relative mobility, using sodium dodecyl sulfate polyacrylamide gel electrophoresis. Gel lanes are then sliced into horizontal sections, and in-gel trypsin digestion performed for each gel slice. Extracted peptides and corresponding proteins are identified using liquid chromatography-tandem mass spectrometry and bioinformatics. Results are compiled in silico to generate a peptograph for every identified protein, being a pictorial representation of sodium dodecyl sulfate polyacrylamide gel electrophoresis. Proteins shown by their peptograph to have migrated further through the gel (i.e., to a lower gel slice) in the lane containing the active protease(s) of interest, as compared to the control, are deemed putative protease substrates. PROTOMAP has broad applicability to a range of experimental conditions and protein pools. Coupling this with its simple and robust methodology, the PROTOMAP approach has emerged as a valuable tool with which to determine protease substrates in complex systems.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 30%
Student > Master 3 30%
Researcher 2 20%
Unspecified 1 10%
Professor > Associate Professor 1 10%
Other 1 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 60%
Chemical Engineering 1 10%
Unspecified 1 10%
Nursing and Health Professions 1 10%
Computer Science 1 10%
Other 1 10%