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全血蛋白质组学分析采用容量吸收微采样进行精准医学生物标志物研究。

Proteomic Analysis of Whole Blood Using Volumetric Absorptive Microsampling for Precision Medicine Biomarker Studies.

机构信息

Bowel Cancer and Biomarker Research Laboratory, School of Medical Sciences, The University of Sydney, Sydney 2065, Australia.

Sangui Bio Pty Ltd., Sydney 2065, Australia.

出版信息

J Proteome Res. 2022 Apr 1;21(4):1196-1203. doi: 10.1021/acs.jproteome.1c00971. Epub 2022 Feb 15.

Abstract

Microsampling of patient blood promises several benefits over conventional phlebotomy practices to facilitate precision medicine studies. These include at-home patient blood collection, supporting telehealth monitoring, minimal postcollection processing, and compatibility with nonrefrigerated transport and storage. However, for proteomic biomarker studies, mass spectrometry of whole blood has generally been avoided in favor of using plasma or serum obtained from venepuncture. We evaluated the use of a volumetric absorptive microsampling (VAMS) device as a sample preparation matrix to enable LC-MS proteomic analyses of dried whole blood. We demonstrated the detection and robust quantitation of up to 1600 proteins from single-shot shotgun-LC-MS analysis of dried whole blood, greatly enhancing proteome depth compared with conventional single-shot LC-MS analyses of undepleted plasma. Some proteins not previously reported in blood were detected using this approach. Various washing reagents were used to demonstrate that proteins can be preferentially removed from VAMS devices prior to downstream analyses. We provide a demonstration that archival frozen blood cell pellets housed under long-term storage (exceeding 5 years) are compatible with VAMS to enable quantitation of potential biomarker proteins from biobank repositories. These demonstrations are important steps in establishing viable analysis workflows to underpin large-scale precision medicine studies. Data are available via ProteomeXchange with the identifier PXD028605.

摘要

微量采血管采血相对于传统静脉采血方法,有望在促进精准医学研究方面带来诸多益处。这些益处包括患者在家中采集血液样本、支持远程医疗监测、采集后处理量最小化,以及与非冷藏运输和储存兼容。然而,对于蛋白质组生物标志物研究,通常避免使用全血进行质谱分析,而是选择使用静脉穿刺获得的血浆或血清。我们评估了使用体积吸收微量采样(VAMS)装置作为样品制备基质,以实现干燥全血的 LC-MS 蛋白质组学分析。我们展示了通过单次Shotgun-LC-MS 分析干燥全血可检测和定量多达 1600 种蛋白质,与常规未稀释血浆的单次 Shot LC-MS 分析相比,大大提高了蛋白质组深度。通过这种方法检测到了一些以前在血液中未报道过的蛋白质。使用各种洗涤试剂进行了演示,表明可以在下游分析之前优先从 VAMS 装置中去除蛋白质。我们提供了一个证明,即长期储存(超过 5 年)的冷冻血细胞沉淀可以与 VAMS 兼容,从而能够从生物库中定量潜在的生物标志物蛋白。这些演示是建立可行的分析工作流程以支持大规模精准医学研究的重要步骤。数据可通过 ProteomeXchange 以标识符 PXD028605 获得。

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