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A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics

BACKGROUND: Neuropeptides are a diverse category of signaling molecules in the nervous system regulating a variety of processes including food intake, social behavior, circadian rhythms, learning, and memory. Both the identification and functional characterization of specific neuropeptides are ongoi...

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Autores principales: Salisbury, Joseph P, Boggio, Kristin J, Hsu, Yun-Wei A, Quijada, Jeniffer, Sivachenko, Anna, Gloeckner, Gabriele, Kowalski, Paul J, Easterling, Michael L, Rosbash, Michael, Agar, Jeffrey N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022047/
https://www.ncbi.nlm.nih.gov/pubmed/24373546
http://dx.doi.org/10.1186/1756-6606-6-60
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author Salisbury, Joseph P
Boggio, Kristin J
Hsu, Yun-Wei A
Quijada, Jeniffer
Sivachenko, Anna
Gloeckner, Gabriele
Kowalski, Paul J
Easterling, Michael L
Rosbash, Michael
Agar, Jeffrey N
author_facet Salisbury, Joseph P
Boggio, Kristin J
Hsu, Yun-Wei A
Quijada, Jeniffer
Sivachenko, Anna
Gloeckner, Gabriele
Kowalski, Paul J
Easterling, Michael L
Rosbash, Michael
Agar, Jeffrey N
author_sort Salisbury, Joseph P
collection PubMed
description BACKGROUND: Neuropeptides are a diverse category of signaling molecules in the nervous system regulating a variety of processes including food intake, social behavior, circadian rhythms, learning, and memory. Both the identification and functional characterization of specific neuropeptides are ongoing fields of research. Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) analysis of nervous tissues from a variety of organisms allows direct detection and identification of neuropeptides. Here, we demonstrate an analysis workflow that allows for the detection of differences in specific neuropeptides amongst a variety of neuropeptides being simultaneously measured. For sample preparation, we describe a straight-forward and rapid (minutes) method where individual adult Drosophila melanogaster brains are analyzed. Using a MATLAB-based data analysis workflow, also compatible with MALDI-TOF mass spectra obtained from other sample preparations and instrumentation, we demonstrate how changes in neuropeptides levels can be detected with this method. RESULTS: Over fifty isotopically resolved ion signals in the peptide mass range are reproducibly observed across experiments. MALDI-TOF MS profile spectra were used to statistically identify distinct relative differences in organ-wide endogenous levels of detected neuropeptides between biological conditions. In particular, three distinct levels of a particular neuropeptide, pigment dispersing factor, were detected by comparing groups of preprocessed spectra obtained from individual brains across three different D. melanogaster strains, each of which express different amounts of this neuropeptide. Using the same sample preparation, MALDI-TOF/TOF tandem mass spectrometry confirmed that at least 14 ion signals observed across experiments are indeed neuropeptides. Among the identified neuropeptides were three products of the neuropeptide-like precursor 1 gene previously not identified in the literature. CONCLUSIONS: Using MALDI-TOF MS and preprocessing/statistical analysis, changes in relative levels of a particular neuropeptide in D. melanogaster tissue can be statistically detected amongst a variety of neuropeptides. While the data analysis methods should be compatible with other sample preparations, the presented sample preparation method was sufficient to identify previously unconfirmed D. melanogaster neuropeptides.
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spelling pubmed-40220472014-05-16 A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics Salisbury, Joseph P Boggio, Kristin J Hsu, Yun-Wei A Quijada, Jeniffer Sivachenko, Anna Gloeckner, Gabriele Kowalski, Paul J Easterling, Michael L Rosbash, Michael Agar, Jeffrey N Mol Brain Methodology BACKGROUND: Neuropeptides are a diverse category of signaling molecules in the nervous system regulating a variety of processes including food intake, social behavior, circadian rhythms, learning, and memory. Both the identification and functional characterization of specific neuropeptides are ongoing fields of research. Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) analysis of nervous tissues from a variety of organisms allows direct detection and identification of neuropeptides. Here, we demonstrate an analysis workflow that allows for the detection of differences in specific neuropeptides amongst a variety of neuropeptides being simultaneously measured. For sample preparation, we describe a straight-forward and rapid (minutes) method where individual adult Drosophila melanogaster brains are analyzed. Using a MATLAB-based data analysis workflow, also compatible with MALDI-TOF mass spectra obtained from other sample preparations and instrumentation, we demonstrate how changes in neuropeptides levels can be detected with this method. RESULTS: Over fifty isotopically resolved ion signals in the peptide mass range are reproducibly observed across experiments. MALDI-TOF MS profile spectra were used to statistically identify distinct relative differences in organ-wide endogenous levels of detected neuropeptides between biological conditions. In particular, three distinct levels of a particular neuropeptide, pigment dispersing factor, were detected by comparing groups of preprocessed spectra obtained from individual brains across three different D. melanogaster strains, each of which express different amounts of this neuropeptide. Using the same sample preparation, MALDI-TOF/TOF tandem mass spectrometry confirmed that at least 14 ion signals observed across experiments are indeed neuropeptides. Among the identified neuropeptides were three products of the neuropeptide-like precursor 1 gene previously not identified in the literature. CONCLUSIONS: Using MALDI-TOF MS and preprocessing/statistical analysis, changes in relative levels of a particular neuropeptide in D. melanogaster tissue can be statistically detected amongst a variety of neuropeptides. While the data analysis methods should be compatible with other sample preparations, the presented sample preparation method was sufficient to identify previously unconfirmed D. melanogaster neuropeptides. BioMed Central 2013-12-27 /pmc/articles/PMC4022047/ /pubmed/24373546 http://dx.doi.org/10.1186/1756-6606-6-60 Text en Copyright © 2013 Salisbury et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Salisbury, Joseph P
Boggio, Kristin J
Hsu, Yun-Wei A
Quijada, Jeniffer
Sivachenko, Anna
Gloeckner, Gabriele
Kowalski, Paul J
Easterling, Michael L
Rosbash, Michael
Agar, Jeffrey N
A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title_full A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title_fullStr A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title_full_unstemmed A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title_short A rapid MALDI-TOF mass spectrometry workflow for Drosophila melanogaster differential neuropeptidomics
title_sort rapid maldi-tof mass spectrometry workflow for drosophila melanogaster differential neuropeptidomics
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022047/
https://www.ncbi.nlm.nih.gov/pubmed/24373546
http://dx.doi.org/10.1186/1756-6606-6-60
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