Guasti P N, Souza F F, Scott C, Papa P M, Camargo L S, Schmith R A, Monteiro G A, Hartwig F P, Papa F O
Department of Veterinary Surgery and Animal Reproduction, School of Veterinary Medicine and Animal Science, FMVZ, São Paulo State University (UNESP), Botucatu, SP, Brazil.
Department of Veterinary Clinic and Surgery, School of Veterinary Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, Brazil.
Theriogenology. 2020 Oct 15;156:70-81. doi: 10.1016/j.theriogenology.2020.06.014. Epub 2020 Jun 14.
During ejaculation, a large amount of seminal plasma proteins interact with the sperm membrane, leading to a series of biochemical and structural changes implicated in sperm function and gamete interaction. However, the roles of the majority of these proteins remain unknown. This study aimed to investigate the proteome and functionality of the major equine proteins of seminal plasma and the sperm membrane. Seminal plasma and enriched-membrane proteins (150 μg) were separated by two-dimensional gel electrophoresis, and the respective maps were analyzed. Protein identification was performed by in-gel digestion and tandem mass spectrometry (GeLC-MS/MS). Samples were also submitted to in-solution digestion (complex protein mixture) and identified by shotgun analysis by LC-MS/MS; bioinformatic tools were used to investigate protein functions. Seminal plasma and sperm membrane extract maps contained 91.0 ± 8.2 spots and 245.3 ± 11.3 spots, respectively, within the 3-10 pH range. In total, the most abundant proteins identified in 2D maps and in complex protein mixtures included 24 proteins for seminal plasma and 33 for sperm membrane extract, with a high degree of confidence (P < 0.05). Of these, HSP1, CRISP3 and KLK1E2 were the most abundant in seminal plasma; HSP1 was highly abundant in sperm membrane extract, in many isoforms, which is related to membrane destabilization and may compromise sperm preservation. HSP1-polybromo-1 interactions suggested a role in DNA stabilization. Prosaposin was identified in seminal plasma and may play a role in the fertilization process. IZUMO4, a member of the IgSF family involved in the prefertilization stages, was identified in 2D gel and MS/MS analysis of sperm membrane extract. Ten proteins of seminal plasma were found to interact with the sperm membrane and were related to binding and catalytic activities (clusterin, CRISP3, epididymal sperm-binding protein 1, kallikrein1E2, seminal plasma protein A3, and HSP1). Additionally, other identified proteins were associated with DNA integrity, capacitation and recognition of pregnancy. These findings indicate that the binding of specific proteins to the plasma membrane during ejaculation may influence sperm survival after cryopreservation and may play a role in decreasing the quality in stallions with toxic seminal plasma. Elucidation of these interactions is an important step in understanding the biological processes related to equine fertility and facilitates future investigations on the selection and application of low freezability semen strategies.
射精过程中,大量精浆蛋白与精子膜相互作用,导致一系列与精子功能和配子相互作用相关的生化和结构变化。然而,这些蛋白中大多数的作用仍不清楚。本研究旨在探究马精浆和精子膜主要蛋白的蛋白质组及功能。通过二维凝胶电泳分离精浆和富集膜蛋白(150μg),并分析各自的图谱。通过胶内消化和串联质谱(GeLC-MS/MS)进行蛋白质鉴定。样品还进行了溶液内消化(复杂蛋白混合物),并通过液相色谱-串联质谱(LC-MS/MS)的鸟枪法分析进行鉴定;使用生物信息学工具研究蛋白质功能。在3-10的pH范围内,精浆图谱和精子膜提取物图谱分别包含91.0±8.2个斑点和245.3±11.3个斑点。总共,在二维图谱和复杂蛋白混合物中鉴定出的最丰富的蛋白质包括精浆中的24种蛋白和精子膜提取物中的33种蛋白,可信度很高(P<0.05)。其中,HSP1、CRISP3和KLK1E2在精浆中最为丰富;HSP1在精子膜提取物中以多种异构体形式高度丰富,这与膜不稳定有关,可能会影响精子保存。HSP1与多溴-1的相互作用表明其在DNA稳定中起作用。在精浆中鉴定出了prosaposin,其可能在受精过程中发挥作用。IZUMO4是免疫球蛋白超家族(IgSF)的成员,参与受精前阶段,在精子膜提取物的二维凝胶和MS/MS分析中被鉴定出来。发现精浆中的10种蛋白与精子膜相互作用,与结合和催化活性相关(簇集蛋白、CRISP3、附睾精子结合蛋白1、激肽释放酶1E2、精浆蛋白A3和HSP1)。此外,其他鉴定出的蛋白与DNA完整性、获能和妊娠识别有关。这些发现表明,射精过程中特定蛋白与质膜的结合可能会影响冷冻保存后精子的存活,并可能在降低有毒精浆种马的精液质量中发挥作用。阐明这些相互作用是理解与马繁殖力相关的生物学过程的重要一步,并有助于未来对低冻融性精液策略的选择和应用的研究。