4.7 Article

Automated Querying and Identification of Novel Peptides using MALDI Mass Spectrometric Imaging

期刊

JOURNAL OF PROTEOME RESEARCH
卷 10, 期 4, 页码 1915-1928

出版社

AMER CHEMICAL SOC
DOI: 10.1021/pr101159e

关键词

mass spectrometry imaging; MALDI imaging; targeted peptide identification

资金

  1. National Center for Research Resources of NIH [P-41-RR24851]
  2. NSF [DBI-0852081]
  3. Centre National de la Recherche Scientifique (CNRS)
  4. Ministere de l'Enseignement, de la Recherche et des Technologies (MERT)
  5. Genoscope
  6. Agence Nationale de la Recherche (ANR)
  7. Div Of Biological Infrastructure
  8. Direct For Biological Sciences [0852081] Funding Source: National Science Foundation

向作者/读者索取更多资源

MSI is a molecular imaging technique that allows for the generation of topographic 2D maps for various endogenous and some exogenous molecules without prior specification of the molecule. In this paper, we start with the premise that a region of interest (ROI) is given to us based on preselected morphological criteria. Given an ROT, we develop a pipeline, first to determine mass values with distinct expression signatures, localized to the ROI, and second to identify the peptides corresponding to these mass values. To identify spatially differentiated masses, we implement a statistic that allows us to estimate, for each spectral peak, the probability that it is over- or under-expressed within the ROI versus outside. To identify peptides corresponding to these masses, we apply LC-MS/MS to fragment endogenous (nonprotease digested) peptides. A novel pipeline based on constructing sequence tags de novo from both original and decharged spectra and a subsequent database search is used to identify peptides. As the MSI signal and the identified peptide are only related by a single mass value, we isolate the corresponding transcript and perform a second validation via in situ hybridization of the transcript. We tested our approach, MSI-Query, on a number of ROIs in the medicinal leech, Hirudo medicinalis, including the central nervous system (CNS). The Hirudo CNS is capable of regenerating itself after injury, thus forming an important model system for neuropeptide identification. The pipeline helps identify a number of novel peptides. Specifically, we identify a gene that we name HmIF4, which is a member of the intermediate filament family involved in neural development and a second novel, uncharacterized peptide. A third peptide, derived from the histone H2B, is also identified, in agreement with the previously suggested role of histone H2B in axon targeting.

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