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一种针对人类血浆蛋白质特征的多重定量蛋白质组学方法。

A Multiplexed Quantitative Proteomics Approach to the Human Plasma Protein Signature.

作者信息

Núñez Estefanía, Gómez-Serrano María, Calvo Enrique, Bonzon-Kulichenko Elena, Trevisan-Herraz Marco, Rodríguez José Manuel, García-Marqués Fernando, Magni Ricardo, Lara-Pezzi Enrique, Martín-Ventura José Luis, Camafeita Emilio, Vázquez Jesús

机构信息

Centro Nacional de Investigaciones Cardiovasculares Carlos III, 28029 Madrid, Spain.

CIBER de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.

出版信息

Biomedicines. 2024 Sep 18;12(9):2118. doi: 10.3390/biomedicines12092118.

Abstract

Despite the plasma proteome being able to provide a unique insight into the health and disease status of individuals, holding singular promise as a source of protein biomarkers that could be pivotal in the context of personalized medicine, only around 100 proteins covering a few human conditions have been approved as biomarkers by the US Food and Drug Administration (FDA) so far. Mass spectrometry (MS) currently has enormous potential for high-throughput analysis in clinical research; however, plasma proteomics remains challenging mainly due to the wide dynamic range of plasma protein abundances and the time-consuming procedures required. We applied a new MS-based multiplexed proteomics workflow to quantitate proteins, encompassing 67 FDA-approved biomarkers, in >1300 human plasma samples from a clinical cohort. Our results indicate that this workflow is suitable for large-scale clinical studies, showing good accuracy and reproducibility (coefficient of variation (CV) < 20 for 90% of the proteins). Furthermore, we identified plasma signature proteins (stable in time on an individual basis), stable proteins (exhibiting low biological variability and high temporal stability), and highly variable proteins (with low temporal stability) that can be used for personalized health monitoring and medicine.

摘要

尽管血浆蛋白质组能够为个体的健康和疾病状况提供独特的见解,作为蛋白质生物标志物的来源具有独特的前景,这在个性化医疗中可能至关重要,但到目前为止,美国食品药品监督管理局(FDA)仅批准了约100种涵盖少数人类疾病状况的蛋白质作为生物标志物。质谱(MS)目前在临床研究的高通量分析方面具有巨大潜力;然而,血浆蛋白质组学仍然具有挑战性,主要是由于血浆蛋白质丰度的动态范围广泛以及所需的耗时程序。我们应用了一种基于质谱的新型多重蛋白质组学工作流程,对来自一个临床队列的1300多个人类血浆样本中的67种FDA批准的生物标志物进行蛋白质定量。我们的结果表明,该工作流程适用于大规模临床研究,显示出良好的准确性和可重复性(90%的蛋白质变异系数(CV)<20)。此外,我们鉴定出了可用于个性化健康监测和医学的血浆特征蛋白(个体水平上随时间稳定)、稳定蛋白(表现出低生物学变异性和高时间稳定性)以及高变蛋白(时间稳定性低)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1c/11428418/d449d94e4344/biomedicines-12-02118-g001.jpg

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