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使用纳米流式细胞术测定水相中的单个病毒和小细胞外囊泡的折射率。

Refractive Index Determination of Individual Viruses and Small Extracellular Vesicles in Aqueous Media Using Nano-Flow Cytometry.

机构信息

Department of Chemical Biology, the MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, the Key Laboratory for Chemical Biology of Fujian Province, Collaborative Innovation Center of Chemistry for Energy Materials, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, People's Republic of China.

出版信息

Anal Chem. 2022 Oct 18;94(41):14299-14307. doi: 10.1021/acs.analchem.2c02833. Epub 2022 Sep 9.

Abstract

The refractive index (RI) is a fundamental physical property of materials. Although measurement of the RI of biological nanoparticles (BNPs) in aqueous media is of great importance to basic research and biomedical applications, it is hampered by their tiny size, large intrinsic heterogeneity, and weak scattering. Here, we report the development of a label-free technique that can determine the RI of individual viruses and small extracellular vesicles (sEVs) with high precision and an analysis rate up to 10 000 particles per minute. This was achieved via the combination of high-sensitivity light-scattering detection by nanoflow cytometry (nFCM) and the Mie theory calculation. With the measured RIs for T7 virions, T7 capsids, and sEVs, the concentrations of nucleic acid in viral particles and protein in the lumen of sEVs were estimated. Furthermore, building upon a simplified core-shell model, the RIs of sEVs ranging from 40 to 200 nm were obtained. By using these RIs, a statistically robust size distribution of sEVs was acquired in minutes with accuracy and resolution matched closely with those of cryo-TEM measurements. Our approach could become an important tool in the RI determination of single BNPs.

摘要

折射率(RI)是材料的基本物理性质。尽管在水介质中测量生物纳米颗粒(BNPs)的 RI 对基础研究和生物医学应用非常重要,但由于其尺寸极小、内在异质性大以及散射弱,这一测量受到了阻碍。在这里,我们报告了一种无标记技术的发展,该技术可以高精度地确定单个病毒和小细胞外囊泡(sEVs)的 RI,每分钟分析速度高达 10000 个颗粒。这是通过纳米流式细胞术(nFCM)的高灵敏度光散射检测与 Mie 理论计算相结合来实现的。通过测量 T7 噬菌体、T7 衣壳和 sEVs 的 RI,估算了病毒颗粒中核酸的浓度和 sEV 腔室中蛋白质的浓度。此外,基于简化的核壳模型,还获得了 40 至 200nm 范围内的 sEVs 的 RI。利用这些 RI,我们可以在几分钟内获得具有统计学意义的 sEV 稳健尺寸分布,其准确性和分辨率与 cryo-TEM 测量非常匹配。我们的方法可能成为单个 BNPs RI 测定的重要工具。

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