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蛋白质吸附损失─单细胞蛋白质组学的瓶颈。

Protein Adsorption Loss─The Bottleneck of Single-Cell Proteomics.

机构信息

Department of Chemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada.

Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada.

出版信息

J Proteome Res. 2022 Aug 5;21(8):1808-1815. doi: 10.1021/acs.jproteome.2c00317. Epub 2022 Jul 18.

Abstract

Single-cell proteomics is a promising field to provide direct yet comprehensive molecular insights into cellular functions without averaging effects. Here, we address a grand technical challenge impeding the maturation of single-cell proteomics─protein adsorption loss (PAL). Even though widely known, there is currently no quantitation on how profoundly and selectively PAL has affected single-cell proteomics. Therefore, the mitigations to this challenge have been generic, and their efficacy was only evaluated by the size of the resolved proteome with no specificity on individual proteins. We use the existing knowledge of PAL, protein expression, and the typical surface area used in single-cell proteomics to discuss the severity of protein loss. We also summarize the current solutions to this challenge and briefly review the available methods to characterize the physical and chemical properties of protein surface adsorption. By citing successful strategies in single-cell genomics for measurement errors in individual transcripts, we pinpoint the urgency to benchmark PAL at the proteome scale with individual protein resolution. Finally, orthogonal single-cell proteomic techniques that have the potential to cross validate PAL are proposed. We hope these efforts can promote the fruition of single-cell proteomics in the near future.

摘要

单细胞蛋白质组学是一个很有前途的领域,它可以提供直接而全面的分子见解,而无需平均效应。在这里,我们解决了一个阻碍单细胞蛋白质组学成熟的重大技术挑战——蛋白质吸附损失(PAL)。尽管广为人知,但目前还没有定量分析 PAL 对单细胞蛋白质组学的影响有多深远和选择性。因此,针对这一挑战的缓解措施是通用的,其效果仅通过解决的蛋白质组的大小来评估,而对单个蛋白质没有特异性。我们利用现有的 PAL、蛋白质表达和单细胞蛋白质组学中常用的典型表面积的知识来讨论蛋白质损失的严重程度。我们还总结了目前解决这一挑战的方法,并简要回顾了用于表征蛋白质表面吸附物理和化学性质的现有方法。通过引用单细胞基因组学中针对单个转录本测量误差的成功策略,我们指出迫切需要在蛋白质组范围内以单个蛋白质分辨率来基准 PAL。最后,提出了具有潜在能力的正交单细胞蛋白质组学技术来交叉验证 PAL。我们希望这些努力能够促进单细胞蛋白质组学在不久的将来取得成果。

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