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Evaluation of protein phosphorylation in bull sperm during their maturation in the epididymis

J. Jankovičová, K. Michalková, P. Sečová, Ľ. Horovská, P. Maňásková-Postlerová, J. Antalíková,

. 2018 ; 371 (2) : 365-373. [pub] 20171023

Jazyk angličtina Země Německo

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc19028711

Grantová podpora
VEGA-2/0037/16 Vedecká Grantová Agentúra MŠVVaŠ SR a SAV - International
APVV-15-0196 Agentúra na Podporu Výskumu a Vývoja - International

E-zdroje Online Plný text

NLK ProQuest Central od 2000-12-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest) od 2000-12-01 do Před 1 rokem
Health & Medicine (ProQuest) od 2000-12-01 do Před 1 rokem

Phosphorylation, or dephosphorylation, is one of the most frequent post-translational modifications regulating protein-protein activity in eukaryotic cells. Whereas mature spermatozoa (as specialized cells) are transcriptionally inactive and do not synthesize new proteins, phosphorylation of sperm proteins is very important for the regulation of the sperm function. Although the post-testicular maturation of spermatozoa is a process common to all mammals, comparative studies showed significant differences in sperm surface proteins and the mechanisms of protein modification during the epididymal maturation. In our study, the evaluation of tyrosine phosphorylation, represented by the fluorescent patterns of used anti-phosphotyrosine antibodies (P-Tyr-01 and 4G10), in spermatozoa isolated from different regions of the epididymis - caput, corpus and cauda - was performed. Although in general both antibodies detected almost the same reaction patterns, we observed some dissimilarity associated with the binding specificity of the antibodies and also the segment-dependent manner of phosphorylated protein localization. These data were filled up by immunohistochemical analysis of testes and epididymides cryosections. Additionally, our phosphoproteomic study focused on evaluation of the changes in the pattern of tyrosine-phosphorylated proteins during the post-testicular maturation of bull spermatozoa (PY20 antibody). To summarize the results, an increasing trend of tyrosine phosphorylation of proteins during the maturation of bull sperm in the epididymis was consistently observed in all the methods/experiments.

Citace poskytuje Crossref.org

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