Doctorado en Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana, Ciudad de México, México.
Departamento de Ciencias de la Salud. D.C.B.S, Universidad Autónoma Metropolitana-Iztapalapa, San Rafael Atlixco 186, Col. Vicentina, C.P, 09340, Ciudad de México, México.
Glycoconj J. 2020 Aug;37(4):499-509. doi: 10.1007/s10719-020-09924-0. Epub 2020 May 4.
The surface of the spermatozoa is coated with glycoproteins the redistribution of which during in vitro capacitation plays a key role in the subsequent fertilization process. Lipid rafts are membrane microdomains involved in signal transduction through receptors and include or recruit specific types of proteins and glycoproteins. Few studies have focused on identifying glycoproteins resident in the lipid rafts of spermatozoa. Proteins associated with lipid rafts modify their localization during capacitation. The objective of the study was to identify the glycoproteins associated with lipid rafts of capacitated boar spermatozoa through a lectin-binding assay coupled to mass spectrometry approach. From the proteomic profiles generated by the raft proteins extractions, we observed that after capacitation the intensity of some bands increased while that of others decreased. To determine whether the proteins obtained from lipid rafts are glycosylated, lectin blot assays were performed. Protein bands with a good resolution and showing significant glycosylation modifications after capacitation were analyzed by mass spectrometry. The bands of interest had an apparent molecular weight of 64, 45, 36, 34, 24, 18 and 15 kDa. We sequenced the 7 bands and 20 known or potential glycoproteins were identified. According to us, for ten of them this is the first time that their association with sperm lipid rafts is described (ADAM5, SPMI, SPACA1, Seminal plasma protein pB1, PSP-I, MFGE8, tACE, PGK2, SUCLA2, MDH1). Moreover, LYDP4, SPAM-1, HSP60, ZPBP1, AK1 were previously reported in lipid rafts of mouse and human spermatozoa but not in boar spermatozoa. We also found and confirmed the presence of ACR, ACRBP, AWN, AQN3 and PRDX5 in lipid rafts of boar spermatozoa. This paper provides an overview of the glycosylation pattern in lipid rafts of boar spermatozoa before and after capacitation. Further glycomic analysis is needed to determine the type and the variation of glycan chains of the lipid rafts glycoproteins on the surface of spermatozoa during capacitation and acrosome reaction.
精子表面覆盖着糖蛋白,这些糖蛋白在体外获能过程中的重新分布在随后的受精过程中起着关键作用。脂筏是参与通过受体进行信号转导的膜微区,包括或募集特定类型的蛋白质和糖蛋白。很少有研究集中在鉴定精子脂筏中的糖蛋白上。与脂筏相关的蛋白质在获能过程中会改变其定位。本研究的目的是通过凝集素结合分析与质谱分析相结合的方法,鉴定获能公猪精子脂筏中的糖蛋白。从提取的脂筏蛋白的蛋白质组学图谱中,我们观察到获能后一些条带的强度增加,而另一些条带的强度降低。为了确定从脂筏中获得的蛋白质是否发生了糖基化,进行了凝集素印迹分析。在获能后具有良好分辨率且显示出显著糖基化修饰的蛋白质条带通过质谱进行分析。感兴趣的条带的表观分子量为 64、45、36、34、24、18 和 15 kDa。我们对 7 条带进行了测序,鉴定出 20 种已知或潜在的糖蛋白。据我们所知,其中 10 种是首次描述它们与精子脂筏的关联(ADAM5、SPMI、SPACA1、精液蛋白 pB1、PSP-I、MFGE8、tACE、PGK2、SUCLA2、MDH1)。此外,LYDP4、SPAM-1、HSP60、ZPBP1、AK1 先前被报道存在于小鼠和人精子的脂筏中,但不存在于公猪精子中。我们还发现并证实了 ACR、ACRBP、AWN、AQN3 和 PRDX5 存在于公猪精子的脂筏中。本文概述了获能前后公猪精子脂筏中的糖基化模式。进一步的糖组学分析需要确定在获能和顶体反应过程中,脂筏糖蛋白表面的精子糖链的类型和变化。