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血清中卵巢癌生物标志物溶血磷脂酸的检测。

Detection of the Ovarian Cancer Biomarker Lysophosphatidic Acid in Serum.

机构信息

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON M5S 3H6, Canada.

出版信息

Biosensors (Basel). 2020 Feb 14;10(2):13. doi: 10.3390/bios10020013.

Abstract

Lysophosphatidic acid (LPA) is present during the medical condition of ovarian cancer at all stages of the disease, and, therefore possesses considerable potential as a biomarker for screening its presence in female patients. Unfortunately, there is currently no assay for this biomarker. In the present work, we introduce a test based on the duel protein system of actin and gelsolin that could allow the quantitative measurement of LPA in serum samples in a biosensing format. In order to evaluate this possibility, actin protein was dye-modified and complexed with gelsolin protein, followed by surface deposition onto silica nanoparticles. This solid-phase system was exposed to serum samples containing various concentrations of LPA and analyzed by fluorescence microscopy. Measurements conducted for the LPA-containing serum samples were higher after exposure to the developed test than samples without LPA. Early results suggest a limit of detection of 5 μM LPA in serum. The eventual goal is to employ the chemistry described here in a biosensor configuration for the large population-scale, rapid screening of women for the potential occurrence of ovarian cancer.

摘要

溶血磷脂酸(LPA)存在于卵巢癌的各个阶段的疾病状态中,因此具有作为女性患者筛查其存在的生物标志物的巨大潜力。不幸的是,目前没有针对该生物标志物的检测方法。在本工作中,我们引入了一种基于肌动蛋白和凝胶蛋白双蛋白系统的测试,可以允许在生物传感格式中定量测量血清样品中的 LPA。为了评估这种可能性,肌动蛋白蛋白被染料修饰并与凝胶蛋白复合,然后沉淀到硅纳米颗粒上。将这个固相系统暴露于含有不同浓度 LPA 的血清样品中,并通过荧光显微镜进行分析。在暴露于开发的测试后,含 LPA 的血清样品的测量值高于不含 LPA 的样品。初步结果表明血清中 LPA 的检测限为 5 μM。最终目标是将这里描述的化学方法应用于生物传感器配置中,用于大规模快速筛选女性是否存在卵巢癌的潜在发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f905/7168251/f71b9e037765/biosensors-10-00013-g001.jpg

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