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Proteomic Profile of Daphnia pulex using Data-Independent Acquisition Mass Spectrometry and Ion Mobility Separation. | LitMetric

AI Article Synopsis

  • Daphnia pulex is crucial for aquatic ecosystems and serves as a key model for ecological and evolutionary studies, but its proteome has not been fully characterized due to challenges in sample preparation and a focus on genome analysis.
  • Various methods of sample handling and mass spectrometry were tested in this study to enhance the exploration of D. pulex proteins, leading to better results when using both in-gel and in-solution trypsin digestion techniques.
  • The findings reveal enriched mitochondrial and hydrolytic functions in D. pulex and identified new proteins that may affect genome modification, with data accessible through ProteomeXchange (PXD008455).

Article Abstract

Daphnia pulex is a keystone species for aquatic habitats and an ecological/evolution model organism. Although significant progress has been made on characterizing its genome, the D. pulex proteome remains largely uncharacterized partially due to abnormally high protein degradation during homogenization and emphasis on genomic analysis. In this study, various sample preparation and mass spectrometry acquisition methods are performed for the purpose of improving D. pulex proteome exploration. Benefits for employing both in-gel and in-solution methods of trypsin digestion are observed. Furthermore, acquisition methods employing ion mobility separation greatly increase peptide identification and more than doubled the proteome coverage. Bioinformatic analysis suggests that mitochondrial and hydrolytic activities are enriched in D. pulex compared to closely related invertebrates or Homo sapiens. Also, novel D. pulex proteins possessing putative genome modifying functional domains are identified. Data are available via ProteomeXchange with identifier PXD008455.

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Source
http://dx.doi.org/10.1002/pmic.201700460DOI Listing

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