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Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling

MALDI profiling and imaging mass spectrometry (IMS) are novel techniques for direct analysis of peptides and small proteins in biological tissues. In this work we applied them to the study of Anopheles gambiae antennae, with the aim of analysing expression of soluble proteins involved in olfaction p...

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Autores principales: Dani, Francesca R., Francese, Simona, Mastrobuoni, Guido, Felicioli, Antonio, Caputo, Beniamino, Simard, Frederic, Pieraccini, Giuseppe, Moneti, Gloriano, Coluzzi, Mario, della Torre, Alessandra, Turillazzi, Stefano
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474704/
https://www.ncbi.nlm.nih.gov/pubmed/18665262
http://dx.doi.org/10.1371/journal.pone.0002822
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author Dani, Francesca R.
Francese, Simona
Mastrobuoni, Guido
Felicioli, Antonio
Caputo, Beniamino
Simard, Frederic
Pieraccini, Giuseppe
Moneti, Gloriano
Coluzzi, Mario
della Torre, Alessandra
Turillazzi, Stefano
author_facet Dani, Francesca R.
Francese, Simona
Mastrobuoni, Guido
Felicioli, Antonio
Caputo, Beniamino
Simard, Frederic
Pieraccini, Giuseppe
Moneti, Gloriano
Coluzzi, Mario
della Torre, Alessandra
Turillazzi, Stefano
author_sort Dani, Francesca R.
collection PubMed
description MALDI profiling and imaging mass spectrometry (IMS) are novel techniques for direct analysis of peptides and small proteins in biological tissues. In this work we applied them to the study of Anopheles gambiae antennae, with the aim of analysing expression of soluble proteins involved in olfaction perireceptor events. MALDI spectra obtained by direct profiling on single antennae and by the analysis of extracts, showed similar profiles, although spectra obtained through profiling had a richer ion population and higher signal to noise ratio. Male and female antennae showed distinct protein profiles. MALDI imaging experiments were also performed and differences were observed in the localization of some proteins. Two proteins were identified through high resolution measurement and top-down MS/MS experiments. A 8 kDa protein only present in the male antennae matched with an unannotated sequence of the An. gambiae genome, while the presence of odorant binding protein 9 (OBP-9) was confirmed through experiments of 2-DE, followed by MS and MS/MS analysis of digested spots. This work shows that MALDI MS profiling is a technique suitable for the analysis of proteins of small and medium MW in insect appendices, and allows obtaining data for several specimens which can be investigated for differences between groups. Proteins of interest can be identified through other complementary MS approaches.
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spelling pubmed-24747042008-07-30 Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling Dani, Francesca R. Francese, Simona Mastrobuoni, Guido Felicioli, Antonio Caputo, Beniamino Simard, Frederic Pieraccini, Giuseppe Moneti, Gloriano Coluzzi, Mario della Torre, Alessandra Turillazzi, Stefano PLoS One Research Article MALDI profiling and imaging mass spectrometry (IMS) are novel techniques for direct analysis of peptides and small proteins in biological tissues. In this work we applied them to the study of Anopheles gambiae antennae, with the aim of analysing expression of soluble proteins involved in olfaction perireceptor events. MALDI spectra obtained by direct profiling on single antennae and by the analysis of extracts, showed similar profiles, although spectra obtained through profiling had a richer ion population and higher signal to noise ratio. Male and female antennae showed distinct protein profiles. MALDI imaging experiments were also performed and differences were observed in the localization of some proteins. Two proteins were identified through high resolution measurement and top-down MS/MS experiments. A 8 kDa protein only present in the male antennae matched with an unannotated sequence of the An. gambiae genome, while the presence of odorant binding protein 9 (OBP-9) was confirmed through experiments of 2-DE, followed by MS and MS/MS analysis of digested spots. This work shows that MALDI MS profiling is a technique suitable for the analysis of proteins of small and medium MW in insect appendices, and allows obtaining data for several specimens which can be investigated for differences between groups. Proteins of interest can be identified through other complementary MS approaches. Public Library of Science 2008-07-30 /pmc/articles/PMC2474704/ /pubmed/18665262 http://dx.doi.org/10.1371/journal.pone.0002822 Text en Dani et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dani, Francesca R.
Francese, Simona
Mastrobuoni, Guido
Felicioli, Antonio
Caputo, Beniamino
Simard, Frederic
Pieraccini, Giuseppe
Moneti, Gloriano
Coluzzi, Mario
della Torre, Alessandra
Turillazzi, Stefano
Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title_full Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title_fullStr Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title_full_unstemmed Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title_short Exploring Proteins in Anopheles gambiae Male and Female Antennae through MALDI Mass Spectrometry Profiling
title_sort exploring proteins in anopheles gambiae male and female antennae through maldi mass spectrometry profiling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474704/
https://www.ncbi.nlm.nih.gov/pubmed/18665262
http://dx.doi.org/10.1371/journal.pone.0002822
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