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开发一种基于液滴的简便单细胞分离平台,用于微生物的培养和基因组分析。

Development of a facile droplet-based single-cell isolation platform for cultivation and genomic analysis in microorganisms.

机构信息

Single-Cell Center, CAS Key Laboratory of Biofuels and Shandong Key Laboratory of Energy Genetics, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, China.

Key Laboratory for Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, China.

出版信息

Sci Rep. 2017 Jan 23;7:41192. doi: 10.1038/srep41192.

Abstract

Wider application of single-cell analysis has been limited by the lack of an easy-to-use and low-cost strategy for single-cell isolation that can be directly coupled to single-cell sequencing and single-cell cultivation, especially for small-size microbes. Herein, a facile droplet microfluidic platform was developed to dispense individual microbial cells into conventional standard containers for downstream analysis. Functional parts for cell encapsulation, droplet inspection and sorting, as well as a chip-to-tube capillary interface were integrated on one single chip with simple architecture, and control of the droplet sorting was achieved by a low-cost solenoid microvalve. Using microalgal and yeast cells as models, single-cell isolation success rate of over 90% and single-cell cultivation success rate of 80% were demonstrated. We further showed that the individual cells isolated can be used in high-quality DNA and RNA analyses at both gene-specific and whole-genome levels (i.e. real-time quantitative PCR and genome sequencing). The simplicity and reliability of the method should improve accessibility of single-cell analysis and facilitate its wider application in microbiology researches.

摘要

单细胞分析的广泛应用受到缺乏一种易于使用且低成本的单细胞分离策略的限制,这种策略可以直接与单细胞测序和单细胞培养相结合,特别是对于小尺寸的微生物。在此,开发了一种简便的液滴微流控平台,可将单个微生物细胞分配到常规标准容器中进行下游分析。细胞封装、液滴检查和分选的功能部分,以及芯片到管的毛细管接口,都集成在一个具有简单结构的单个芯片上,通过低成本的电磁阀微阀实现液滴分选的控制。使用微藻和酵母细胞作为模型,证明了超过 90%的单细胞分离成功率和 80%的单细胞培养成功率。我们进一步表明,分离的单个细胞可用于高质量的 DNA 和 RNA 分析,包括基因特异性和全基因组水平(即实时定量 PCR 和基因组测序)。该方法的简单性和可靠性应该提高单细胞分析的可及性,并促进其在微生物学研究中的更广泛应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70c/5253770/2a929621221c/srep41192-f1.jpg

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