Suppr超能文献

用于血清游离DNA大小分析的单分子自由溶液流体动力学分离

Single Molecule Free Solution Hydrodynamic Separation for Size Profiling of Serum Cell-Free DNA.

作者信息

Li Andrew, Friedrich Sarah M, Wang Tza-Huei

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2018 Jul;2018:4476-4479. doi: 10.1109/EMBC.2018.8513143.

Abstract

Circulating cell-free DNA (cfDNA) has accumulated significant interest as a noninvasive biomarker. One important accessible parameter, the cfDNA size distribution, appears to be of significant value. Here, we introduce our single molecule free solution hydrodynamic separation platform (SML-FSHS) for robust characterization of the cfDNA size profile from human serum. The platform utilizes hydrodynamic separation for DNA sizing and cylindrical illumination confocal spectroscopy (CICS) for highly sensitive single molecule detection and quantification of DNA molecules. We first used a custom wide dynamic range DNA ladder (50 bp-23 kbp) stained with an intercalating dye to create a calibration curve relating DNA retention time to DNA size in base pairs. From this, we demonstrate that the system can profile the cfDNA size distributions in a clinical sample with wide sizing dynamic range and high resolution ~5% of fragment length) all in a single run. The method consumes negligible (3pL) volume of precious sample and minimizes sample processing bias that affects other methods such as PCR and sequencing. We also compare the cfDNA size distributions from stage 1V cancer patients with normal patient samples and demonstrate that specific cfDNA size ranges may correlate with disease state. In addition, we can absolutely quantify cfDNA and gate out the contributions of cellular contamination by size. With these properties, we believe that this platform can help to accelerate future circulating DNA research.

摘要

循环游离DNA(cfDNA)作为一种非侵入性生物标志物已引起广泛关注。一个重要的可获取参数,即cfDNA大小分布,似乎具有重要价值。在此,我们介绍我们的单分子自由溶液流体动力学分离平台(SML-FSHS),用于从人血清中稳健地表征cfDNA大小谱。该平台利用流体动力学分离进行DNA大小测定,并利用柱面照明共聚焦光谱(CICS)对DNA分子进行高灵敏度单分子检测和定量。我们首先使用一种用嵌入染料染色的定制宽动态范围DNA梯(50 bp - 23 kbp)来创建一条校准曲线,将DNA保留时间与碱基对中的DNA大小相关联。由此,我们证明该系统能够在单次运行中以宽大小动态范围和高分辨率(片段长度的约5%)描绘临床样本中的cfDNA大小分布。该方法消耗的珍贵样本体积可忽略不计(3 pL),并将影响其他方法(如PCR和测序)的样本处理偏差降至最低。我们还比较了IV期癌症患者与正常患者样本的cfDNA大小分布,并证明特定的cfDNA大小范围可能与疾病状态相关。此外,我们可以绝对定量cfDNA,并通过大小排除细胞污染的影响。基于这些特性,我们相信该平台有助于加速未来的循环DNA研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验