posted on 2017-09-11, 00:00authored byChristine Carapito, Paula Duek, Charlotte Macron, Marine Seffals, Karine Rondel, François Delalande, Cecilia Lindskog, Thomas Fréour, Yves Vandenbrouck, Lydie Lane, Charles Pineau
The
present study is a contribution to the “neXt50 challenge”,
a coordinated effort across C-HPP teams to identify the 50 most tractable
missing proteins (MPs) on each chromosome. We report the targeted
search of 38 theoretically detectable MPs from chromosomes 2 and 14
in Triton X-100 soluble and insoluble sperm fractions from a total
of 15 healthy donors. A targeted mass-spectrometry-based strategy
consisting of the development of LC–PRM assays (with heavy
labeled synthetic peptides) targeting 92 proteotypic peptides of the
38 selected MPs was used. Out of the 38 selected MPs, 12 were identified
with two or more peptides and 3 with one peptide after extensive SDS-PAGE
fractionation of the two samples and with overall low-intensity signals.
The PRM data are available via ProteomeXchange in PASSEL (PASS01013).
Further validation by immunohistochemistry on human testes sections
and cytochemistry on sperm smears was performed for eight MPs with
antibodies available from the Human Protein Atlas. Deep analysis of
human sperm still allows the validation of MPs and therefore contributes
to the C-HPP worldwide effort. We anticipate that our results will
be of interest to the reproductive biology community because an in-depth
analysis of these MPs may identify potential new candidates in the
context of human idiopathic infertilities.