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使用反相蛋白质阵列定量生物标志物蛋白。

Quantification of Biomarker Proteins Using Reverse-Phase Protein Arrays.

机构信息

National Cancer Center Research Institute, Tokyo, 104-0045, Japan.

Department of Gastrointestinal and Pediatric Surgery, Tokyo Medical University, Tokyo, 160-0023, Japan.

出版信息

Proteomics Clin Appl. 2020 Jul;14(4):e1900120. doi: 10.1002/prca.201900120. Epub 2020 Feb 28.

Abstract

It is expected that antibody-based proteomics will soon occupy a pivotal position in the discovery and validation of biomarkers and therapeutic targets. The reverse-phase protein array (RPPA) is an antibody-based proteomic method that can quantify the expression of multiple posttranslationally modified proteins (such as those that have been phosphorylated) across a large number of protein samples. RPPA is highly sensitive and requires only very small protein samples. This feature, in combination with large antibody libraries, makes RPPA ideal for clinical proteomics, as well as the fact that it is an expandable multiplex assay. In Volume 14, Issue 1 of Proteomics Clinical Applications, Suzuki and colleagues report for the first time a study comparing RPPA and immunohistochemistry for quantification of seven biomarker proteins used for subtyping of diffuse large B-cell lymphoma. Such combination of multiple biomarkers is likely to increase diagnostic accuracy and can be used for precise classification of this heterogeneous disease.

摘要

预计基于抗体的蛋白质组学将很快在生物标志物和治疗靶点的发现和验证中占据关键地位。反相蛋白质阵列 (RPPA) 是一种基于抗体的蛋白质组学方法,可以定量检测大量蛋白质样本中多种翻译后修饰蛋白(如磷酸化蛋白)的表达。RPPA 具有很高的灵敏度,仅需非常少量的蛋白质样本。这一特点,再加上大量的抗体库,使得 RPPA 非常适合临床蛋白质组学,而且它还是一种可扩展的多重分析方法。在《蛋白质组学临床应用》第 14 卷第 1 期,Suzuki 及其同事首次报道了一项研究,比较了 RPPA 和免疫组织化学用于定量检测七种用于弥漫性大 B 细胞淋巴瘤分型的生物标志物蛋白。这种多种生物标志物的组合可能会提高诊断准确性,并可用于对这种异质性疾病进行精确分类。

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