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MALDI-TOF MS protein fingerprinting of mixed samples

Analytical techniques currently available for the characterization of mixtures of microorganisms are generally based on next-generation sequencing. Motivated to develop practical and less-expensive methods for characterizing such mixtures, we propose, as an alternative or complement, the use of matr...

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Autores principales: Reeve, Michael A, Bachmann, Denise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200911/
https://www.ncbi.nlm.nih.gov/pubmed/32395630
http://dx.doi.org/10.1093/biomethods/bpz013
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author Reeve, Michael A
Bachmann, Denise
author_facet Reeve, Michael A
Bachmann, Denise
author_sort Reeve, Michael A
collection PubMed
description Analytical techniques currently available for the characterization of mixtures of microorganisms are generally based on next-generation sequencing. Motivated to develop practical and less-expensive methods for characterizing such mixtures, we propose, as an alternative or complement, the use of matrix-assisted laser-desorption and ionization time-of-flight mass spectrometry (MALDI-TOF MS), which is capable of high-resolution discrimination between species and even between biotypes within species. Potential approaches employing this technique for such characterization are discussed along with impediments to their successful employment. As a consequence, our rationale has been to capitalize on the powerful algorithms currently available for spectral comparison. Following this rationale, the first priority is to ensure the generation of MALDI-TOF MS spectra from mixtures of microorganisms that contain manageable peak complexities and that can be handled by the existing spectral comparison algorithms, preferably with the option to archive and re-run sample preparations and to pipette replicates of these onto MALDI-TOF MS sample plates. The second priority is to ensure that database entry is comparably facile to sample preparation so that large databases of known microorganism mixture MALDI-TOF MS spectra could be readily prepared for comparison with the spectra of unknown mixtures. In this article, we address the above priorities and generate illustrative MALDI-TOF MS spectra to demonstrate the utility of this approach. In addition, we investigate methods aimed at chemically modulating the peak complexity of the obtained MALDI-TOF MS spectra.
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spelling pubmed-72009112020-05-11 MALDI-TOF MS protein fingerprinting of mixed samples Reeve, Michael A Bachmann, Denise Biol Methods Protoc Methods Manuscript Analytical techniques currently available for the characterization of mixtures of microorganisms are generally based on next-generation sequencing. Motivated to develop practical and less-expensive methods for characterizing such mixtures, we propose, as an alternative or complement, the use of matrix-assisted laser-desorption and ionization time-of-flight mass spectrometry (MALDI-TOF MS), which is capable of high-resolution discrimination between species and even between biotypes within species. Potential approaches employing this technique for such characterization are discussed along with impediments to their successful employment. As a consequence, our rationale has been to capitalize on the powerful algorithms currently available for spectral comparison. Following this rationale, the first priority is to ensure the generation of MALDI-TOF MS spectra from mixtures of microorganisms that contain manageable peak complexities and that can be handled by the existing spectral comparison algorithms, preferably with the option to archive and re-run sample preparations and to pipette replicates of these onto MALDI-TOF MS sample plates. The second priority is to ensure that database entry is comparably facile to sample preparation so that large databases of known microorganism mixture MALDI-TOF MS spectra could be readily prepared for comparison with the spectra of unknown mixtures. In this article, we address the above priorities and generate illustrative MALDI-TOF MS spectra to demonstrate the utility of this approach. In addition, we investigate methods aimed at chemically modulating the peak complexity of the obtained MALDI-TOF MS spectra. Oxford University Press 2019-09-25 /pmc/articles/PMC7200911/ /pubmed/32395630 http://dx.doi.org/10.1093/biomethods/bpz013 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Manuscript
Reeve, Michael A
Bachmann, Denise
MALDI-TOF MS protein fingerprinting of mixed samples
title MALDI-TOF MS protein fingerprinting of mixed samples
title_full MALDI-TOF MS protein fingerprinting of mixed samples
title_fullStr MALDI-TOF MS protein fingerprinting of mixed samples
title_full_unstemmed MALDI-TOF MS protein fingerprinting of mixed samples
title_short MALDI-TOF MS protein fingerprinting of mixed samples
title_sort maldi-tof ms protein fingerprinting of mixed samples
topic Methods Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200911/
https://www.ncbi.nlm.nih.gov/pubmed/32395630
http://dx.doi.org/10.1093/biomethods/bpz013
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