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Session: Parallel session 9 - Top-down and Structural analysis

Sperm is still a relevant source for detecting Missing Proteins in the context of the Chromosome-Centric Human Proteome Project

Océane GIRARD 3, Christine CARAPITO4, Charles PINEAU1,2, Régis LAVIGNE1,2, Charline KELLER4, Lila GELY5, Emmanuelle COM1,2, Blandine GUÉVEL1,2, Pierre-Olivier SCHMIT6, Quentin ENJALBERT7, Thomas FRÉOUR3,5

1Univ Rennes, Inserm, EHESP, Irset - UMR_S 1085, Rennes, France
2Univ Rennes, CNRS, Inserm, Biosit UAR 3480 US_S 018, Protim Core Facility, Rennes, France
3Nantes University, CHU Nantes, Inserm, CR2TI, , Nantes, France
4Laboratoire de Spectrométrie de Masse BioOrganique, IPHC, CNRS, Strasbourg, France
5CHU Nantes, Service de Biologie de la Reproduction, Nantes, France
6Bruker Daltonique SA, Wissembourg, France
7PreOmics GmbH, Planegg, Germany

The Chromosome-centric Human Proteome Project (C-HPP) aims at identifying the proteins as gene products encoded by the human genome, characterizing their isoforms and functions. The existence of products has now been confirmed for 93.1% of the genes at the protein level. The remaining mostly correspond to proteins of low abundance or difficult to access. Over the past decade, we have significantly contributed to the identification of over 300 missing proteins in the human sperm. Thanks to technical progresses in mass spectrometry and to the development of efficient sample preparation, we have been able to push further our MS analyses of the human spermatozoa, with the aim to identify new missing proteins. Interestingly, we were able to characterize additional missing proteins using the TimsTOF Ultra coupled to a NanoElute but also using the TimsTOF Pro coupled to a NanoElute based on seven different sample preparations with PreOmics kits. Here, we present the characterization of 9 new missing proteins, and can also propose 12 one-hit wonders proteins, thus contributing again to the efforts of the C-HPP.