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Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks

Despite recent improvements to in situ proteolysis strategies, a higher efficiency is still needed to increase both the number of peptides detected and the associated ion intensity, leading to a complete and reliable set of biomarkers for diagnostic or prognostic purposes. In the study presented her...

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Autores principales: Patel, Ekta, Clench, Malcolm R., West, Andy, Marshall, Peter S., Marshall, Nathan, Francese, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422860/
https://www.ncbi.nlm.nih.gov/pubmed/25916599
http://dx.doi.org/10.1007/s13361-015-1140-z
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author Patel, Ekta
Clench, Malcolm R.
West, Andy
Marshall, Peter S.
Marshall, Nathan
Francese, Simona
author_facet Patel, Ekta
Clench, Malcolm R.
West, Andy
Marshall, Peter S.
Marshall, Nathan
Francese, Simona
author_sort Patel, Ekta
collection PubMed
description Despite recent improvements to in situ proteolysis strategies, a higher efficiency is still needed to increase both the number of peptides detected and the associated ion intensity, leading to a complete and reliable set of biomarkers for diagnostic or prognostic purposes. In the study presented here, an extract of a systematic study is illustrated investigating a range of surfactants assisting trypsin proteolytic activity. Method development was trialled on fingermarks; this specimen results from a transfer of sweat from an individual’s fingertip to a surface upon contact. As sweat carries a plethora of biomolecules, including peptides and proteins, fingermarks are, potentially, a very valuable specimen for non-invasive prognostic or diagnostic screening. A recent study has demonstrated the opportunity to quickly detect peptides and small proteins in fingermarks using Matrix Assisted Laser Desorption Ionization Mass Spectrometry Profiling (MALDI MSP). However, intact detection bears low sensitivity and does not allow species identification; therefore, a shotgun proteomic approach was employed involving in situ proteolysis. Data demonstrate that in fingermarks, further improvements to the existing method can be achieved using MEGA-8 as surfactant in higher percentages as well as combinations of different detergents. Also, for the first time, Rapigest SF, normally used in solution digestions, has been shown to successfully work also for in situ proteolysis. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13361-015-1140-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-44228602015-05-13 Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks Patel, Ekta Clench, Malcolm R. West, Andy Marshall, Peter S. Marshall, Nathan Francese, Simona J Am Soc Mass Spectrom Focus: Imaging Mass Spectrometry: Research Article Despite recent improvements to in situ proteolysis strategies, a higher efficiency is still needed to increase both the number of peptides detected and the associated ion intensity, leading to a complete and reliable set of biomarkers for diagnostic or prognostic purposes. In the study presented here, an extract of a systematic study is illustrated investigating a range of surfactants assisting trypsin proteolytic activity. Method development was trialled on fingermarks; this specimen results from a transfer of sweat from an individual’s fingertip to a surface upon contact. As sweat carries a plethora of biomolecules, including peptides and proteins, fingermarks are, potentially, a very valuable specimen for non-invasive prognostic or diagnostic screening. A recent study has demonstrated the opportunity to quickly detect peptides and small proteins in fingermarks using Matrix Assisted Laser Desorption Ionization Mass Spectrometry Profiling (MALDI MSP). However, intact detection bears low sensitivity and does not allow species identification; therefore, a shotgun proteomic approach was employed involving in situ proteolysis. Data demonstrate that in fingermarks, further improvements to the existing method can be achieved using MEGA-8 as surfactant in higher percentages as well as combinations of different detergents. Also, for the first time, Rapigest SF, normally used in solution digestions, has been shown to successfully work also for in situ proteolysis. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13361-015-1140-z) contains supplementary material, which is available to authorized users. Springer US 2015-04-28 2015 /pmc/articles/PMC4422860/ /pubmed/25916599 http://dx.doi.org/10.1007/s13361-015-1140-z Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Focus: Imaging Mass Spectrometry: Research Article
Patel, Ekta
Clench, Malcolm R.
West, Andy
Marshall, Peter S.
Marshall, Nathan
Francese, Simona
Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title_full Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title_fullStr Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title_full_unstemmed Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title_short Alternative Surfactants for Improved Efficiency of In Situ Tryptic Proteolysis of Fingermarks
title_sort alternative surfactants for improved efficiency of in situ tryptic proteolysis of fingermarks
topic Focus: Imaging Mass Spectrometry: Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422860/
https://www.ncbi.nlm.nih.gov/pubmed/25916599
http://dx.doi.org/10.1007/s13361-015-1140-z
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