Comprehensive quantitative characterization of the human term amnion proteome

Q1 Medicine Matrix Biology Plus Pub Date : 2021-12-01 DOI:10.1016/j.mbplus.2021.100084
Eva Avilla-Royo , Katharina Gegenschatz-Schmid , Jonas Grossmann , Tobias Kockmann , Roland Zimmermann , Jess Gerrit Snedeker , Nicole Ochsenbein-Kölble , Martin Ehrbar
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引用次数: 2

Abstract

The loss of fetal membrane (FM) integrity and function at an early time point during pregnancy can have devastating consequences for the fetus and the newborn. However, biomaterials for preventive sealing and healing of FMs are currently non-existing, which can be partly attributed to the current fragmentary knowledge of FM biology. Despite recent advances in proteomics analysis, a robust and comprehensive description of the amnion proteome is currently lacking. Here, by an optimized protein sample preparation and offline fractionation before liquid chromatography coupled to mass spectrometry (LC-MS) analysis, we present a characterization of the healthy human term amnion proteome, which covers more than 40% of the previously reported transcripts in similar RNA sequencing datasets and, with more than 5000 identifications, greatly outnumbers previous reports. Together, beyond providing a basis for the study of compromised and preterm ruptured FMs, this comprehensive human amnion proteome is a stepping-stone for the development of novel healing-inducing biomaterials. The proteomic dataset has been deposited in the ProteomeXchange Consortium with the identifier PXD019410.

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人足月羊膜蛋白质组的综合定量表征
妊娠早期胎膜完整性和功能的丧失会对胎儿和新生儿造成毁灭性的后果。然而,目前尚不存在用于FMs预防性密封和愈合的生物材料,这在一定程度上可归因于目前对FMs生物学的片面了解。尽管最近在蛋白质组学分析方面取得了进展,但目前还缺乏对羊膜蛋白质组的健全和全面的描述。在这里,通过优化的蛋白质样品制备和液相色谱-质谱(LC-MS)分析之前的离线分离,我们提出了健康人类羊膜蛋白质组的表征,其中涵盖了类似RNA测序数据集中先前报道的转录本的40%以上,并且有超过5000个鉴定,大大超过了之前的报道。总之,除了为受损和过早破裂的FMs提供研究基础之外,这个全面的人羊膜蛋白质组是开发新型诱导愈合生物材料的基石。蛋白质组学数据集已在ProteomeXchange Consortium中保存,标识符为PXD019410。
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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
期刊最新文献
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