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微管在纳米蛋白质组学样品制备中的结合偏好评估。

Evaluation of the Binding Preference of Microtubes for Nanoproteomics Sample Preparation.

机构信息

College of Pharmacy, University of Illinois at Chicago, Chicago, Illinois 60612, United States.

出版信息

J Proteome Res. 2023 Jan 6;22(1):279-284. doi: 10.1021/acs.jproteome.2c00477. Epub 2022 Dec 1.

Abstract

Nonspecific binding between the protein and the container is an often-neglected cause of sample loss in large-scale proteomics sample preparation. In nanoproteomics, due to the small sample size, this absorption loss is no longer negligible, and researchers often adopt low binding plasticware to minimize the sample loss. However, there has been little discussion in the scientific literature on the differences in microtube performance on reducing protein/peptide binding. Therefore, the exact impact of sample loss during the sample preparation is not well understood. Here, we investigated the protein/peptide loss during the nanoproteomics experiment process. Our results showed that there are significant differences in nonspecific binding among the tested microtubes, with a protein recovery rate ranging from less than 10% to over 90% for different microtubes. Interestingly, we found that the storage temperature could also be one of the key factors that contribute to protein recovery from the plastic container. In addition, we investigated the binding preferences of different microtubes by the physical characteristics of the identified proteins and peptides, such as isoelectric point, hydrophobicity, length, and charge. Our findings help to better understand protein/peptide loss in proteomics sample preparation and provide further guidance for researchers in choosing proper containers for their precious sample.

摘要

蛋白质与容器之间的非特异性结合是大规模蛋白质组学样品制备中样品损失经常被忽视的原因。在纳米蛋白质组学中,由于样品量小,这种吸收损失不再可以忽略不计,研究人员通常采用低结合塑料器皿来最大程度地减少样品损失。然而,科学界很少讨论微管在减少蛋白质/肽结合方面的性能差异。因此,对于样品制备过程中样品损失的确切影响还不是很清楚。在这里,我们研究了纳米蛋白质组学实验过程中的蛋白质/肽损失。我们的结果表明,在测试的微管之间存在明显的非特异性结合差异,不同微管的蛋白质回收率从不到 10%到超过 90%不等。有趣的是,我们发现储存温度也可能是导致蛋白质从塑料容器中回收的关键因素之一。此外,我们还通过鉴定出的蛋白质和肽的物理特性,如等电点、疏水性、长度和电荷,研究了不同微管的结合偏好。我们的研究结果有助于更好地理解蛋白质组学样品制备过程中的蛋白质/肽损失,并为研究人员选择合适的容器保存珍贵的样品提供了进一步的指导。

相似文献

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Nanoproteomics comes of age.纳米蛋白质组学崭露头角。
Expert Rev Proteomics. 2018 Nov;15(11):865-871. doi: 10.1080/14789450.2018.1537787. Epub 2018 Oct 30.

本文引用的文献

1
Protein Adsorption Loss─The Bottleneck of Single-Cell Proteomics.蛋白质吸附损失─单细胞蛋白质组学的瓶颈。
J Proteome Res. 2022 Aug 5;21(8):1808-1815. doi: 10.1021/acs.jproteome.2c00317. Epub 2022 Jul 18.
3
The emerging landscape of single-molecule protein sequencing technologies.新兴的单分子蛋白质测序技术领域。
Nat Methods. 2021 Jun;18(6):604-617. doi: 10.1038/s41592-021-01143-1. Epub 2021 Jun 7.
4
Single cell transcriptomics comes of age.单细胞转录组学时代的到来。
Nat Commun. 2020 Aug 27;11(1):4307. doi: 10.1038/s41467-020-18158-5.
9
Adsorption of cationic peptides to solid surfaces of glass and plastic.阳离子肽在玻璃和塑料固体表面的吸附。
PLoS One. 2015 May 1;10(5):e0122419. doi: 10.1371/journal.pone.0122419. eCollection 2015.

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