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首页> 外文期刊>Journal of proteome research >Molecular Pathways Associated with Sperm Biofunction Are Not Affected by the Presence of Round Cell and Leukocyte Proteins in Human Sperm Proteome
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Molecular Pathways Associated with Sperm Biofunction Are Not Affected by the Presence of Round Cell and Leukocyte Proteins in Human Sperm Proteome

机译:与精子生物功能相关的分子途径不受人精子蛋白质组中圆细胞和白细胞蛋白质的影响

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摘要

In human sperm proteomic experiments, leukocyte and round cell proteins may contaminate the sperm proteome and affect the bioinformatic results. The main objective of this study was to identify the possible interference of these proteins, especially from leukocytes, in identification of sperm functional pathways through proteomic and bioinformatic tools. We have evaluated the sperm proteome by liquid chromatography tandem mass spectrometry (LC-MS/MS) in four groups: (1) neat semen with round cells and leukocytes >= 1 x 10(6)/mL; (2) samples with round cells and leukocytes >= 1 x 10(6)/mL processed by 65% density gradient centrifugation; (3) neat semen with round cells <1 x 10(6)/mL; and (4) samples with round cells <1 x 10(6)/mL processed by 65% density gradient centrifugation. Pure leukocyte culture was used as a control group. The difference in the conserved DEPs (common to both sperm and leukocytes) between the sperm samples with leukocytes >1 x 10(6)/mL and round cells <1 x 10(6)/mL was negligible. Comparative analysis between groups 1, 2, 3, and 4 with the control group revealed that the presence of leukocyte proteins does not significantly alter the activation z-score of the identified canonical pathways or biological functions in sperm proteome. Our experimental results demonstrate that the presence of round cell and leukocyte proteins do not affect the identification of the molecular pathways associated with human spermatozoa protein function. Hence, the use of neat frozen semen samples for proteomic studies showed no significant impact on the downstream bioinformatic analysis.
机译:在人精子蛋白质组学实验中,白细胞和圆形细胞蛋白可以污染精子蛋白质组并影响生物信息结果。本研究的主要目的是鉴定这些蛋白质,尤其是白细胞的可能干扰,鉴定通过蛋白质组学和生物信息工具的精子官能途径。通过四组液相色谱串联质谱(LC-MS / MS)评估精子蛋白质:(1)圆细胞和白细胞的整齐精液> = 1×10(6)/ mL; (2)用圆形细胞和白细胞的样品> = 1×10(6)/ mL加工65%密度梯度离心; (3)圆形细胞的整洁精液<1×10(6)/ mL; (4)用65%密度梯度离心处理的圆形细胞<1×10(6)/ mL的样品。纯白细胞培养物用作对照组。使用白细胞的精子样品与白细胞> 1×10(6)/ mL和圆细胞<1×10(6)/ mL之间的保守的DEPS(两种精子和白细胞)的差异可忽略不计。对于对照组的组1,2,3和4之间的比较分析显示,对照组的存在不会显着改变所鉴定的典型途径或精子蛋白质中的生物学功能的激活Z分数。我们的实验结果表明,圆细胞和白细胞蛋白质的存在不会影响与人精子蛋白功能相关的分子途径的鉴定。因此,使用整洁的冷冻精液样品对蛋白质组学研究表明对下游生物信息分析没有显着影响。

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