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通过对单个人类细胞的蛋白质组分析生成的飞行时间碎片谱不表现出非典型的碎片模式。

Time-of-Flight Fragmentation Spectra Generated by the Proteomic Analysis of Single Human Cells Do Not Exhibit Atypical Fragmentation Patterns.

机构信息

The Department of Pharmacology and Molecular SciencesThe Johns Hopkins University School of Medicine, Baltimore, Maryland21205, United States.

出版信息

J Proteome Res. 2023 Mar 3;22(3):1003-1008. doi: 10.1021/acs.jproteome.2c00715. Epub 2023 Jan 26.

Abstract

Recent work detailed the unique characteristics of fragmentation spectra derived from peptides from single human cells. This valuable report utilized an ultrahigh-field Orbitrap and directly compared the spectra obtained from high-concentration bulk cell HeLa lysates to those obtained from nanogram dilutions of the same and from nanowell-processed single HeLa cells. The analysis demonstrated marked differences between the fragmentation spectra generated at high and single-cell loads, most strikingly, the loss of high-mass y-series fragment ions. As significant differences exist in the physics of Orbitrap and time-of-flight mass analyzers, a comparison appeared warranted. A similar analysis was performed using isolated single pancreatic cancer cells compared to pools consisting of 100 cells. While a reanalysis of the prior Orbitrap data supports the author's original findings, the same trends are not observed in time-of-flight mass spectra of peptides from single human cells. The results are particularly striking when directly comparing the matched intensity fragment values between bulk and single-cell data generated on the same mass analyzers. Instrument acquisition files, processed data, and spectrum libraries are publicly available on MASSIVE via accession MSV000090635.

摘要

最近的工作详细描述了源自单个人类细胞肽的碎片化谱的独特特征。这份有价值的报告利用了超高场轨道阱,并直接比较了从高浓度的细胞 HeLa 粗提物中获得的光谱与相同物质的纳克稀释液以及从纳孔处理的单个 HeLa 细胞中获得的光谱。分析表明,在高浓度和单细胞负载下产生的碎片化谱之间存在明显差异,最显著的是,高质量 y 系列碎片离子的丢失。由于轨道阱和飞行时间质量分析仪的物理性质存在显著差异,因此似乎需要进行比较。使用分离的单个胰腺癌细胞与由 100 个细胞组成的池进行了类似的分析。虽然对先前的轨道阱数据进行了重新分析,但在来自单个人类细胞的肽的飞行时间质谱中并未观察到相同的趋势。当直接比较在相同质量分析仪上生成的批量和单细胞数据之间的匹配强度碎片值时,结果尤其引人注目。仪器采集文件、处理后的数据和谱库可通过访问号 MSV000090635 在 MASSIVE 上公开获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6a6/10502792/9903ba6b8a1b/pr2c00715_0001.jpg

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