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高通量细胞生物学的开源 FACS 自动化系统。

An open-source FACS automation system for high-throughput cell biology.

机构信息

Chan Zuckerberg Biohub-San Francisco, San Francisco, California, United States of America.

Medical Business Group, Sony Corporation, San Jose, California, United States of America.

出版信息

PLoS One. 2024 Mar 21;19(3):e0299402. doi: 10.1371/journal.pone.0299402. eCollection 2024.

DOI:10.1371/journal.pone.0299402
PMID:38512845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10956866/
Abstract

Recent advances in gene editing are enabling the engineering of cells with an unprecedented level of scale. To capitalize on this opportunity, new methods are needed to accelerate the different steps required to manufacture and handle engineered cells. Here, we describe the development of an integrated software and hardware platform to automate Fluorescence-Activated Cell Sorting (FACS), a central step for the selection of cells displaying desired molecular attributes. Sorting large numbers of samples is laborious, and, to date, no automated system exists to sequentially manage FACS samples, likely owing to the need to tailor sorting conditions ("gating") to each individual sample. Our platform is built around a commercial instrument and integrates the handling and transfer of samples to and from the instrument, autonomous control of the instrument's software, and the algorithmic generation of sorting gates, resulting in walkaway functionality. Automation eliminates operator errors, standardizes gating conditions by eliminating operator-to-operator variations, and reduces hands-on labor by 93%. Moreover, our strategy for automating the operation of a commercial instrument control software in the absence of an Application Program Interface (API) exemplifies a universal solution for other instruments that lack an API. Our software and hardware designs are fully open-source and include step-by-step build documentation to contribute to a growing open ecosystem of tools for high-throughput cell biology.

摘要

基因编辑技术的最新进展使细胞工程达到了前所未有的规模。为了利用这一机会,需要新的方法来加速制造和处理工程细胞所需的不同步骤。在这里,我们描述了一个集成软件和硬件平台的开发,该平台可自动执行荧光激活细胞分选(FACS),这是选择显示所需分子特征的细胞的关键步骤。对大量样本进行排序是一项繁琐的工作,迄今为止,还没有自动化系统可以顺序管理 FACS 样本,这可能是因为需要根据每个样本的情况来定制分选条件(“门控”)。我们的平台基于商用仪器构建,集成了对仪器上、下游样本的处理和传输、仪器软件的自主控制以及分选门的算法生成,实现了无人值守的功能。自动化消除了操作人员的错误,通过消除操作人员之间的差异标准化了门控条件,并将手工劳动减少了 93%。此外,我们在没有应用程序接口(API)的情况下自动化商用仪器控制软件操作的策略为其他缺乏 API 的仪器提供了通用的解决方案。我们的软件和硬件设计完全开源,并包括逐步构建文档,为高通量细胞生物学工具的不断增长的开放生态系统做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/f01a82957476/pone.0299402.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/f534fa1ac545/pone.0299402.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/34fc66c71cc0/pone.0299402.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/6d3f36368c84/pone.0299402.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/f01a82957476/pone.0299402.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/f534fa1ac545/pone.0299402.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/34fc66c71cc0/pone.0299402.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/6d3f36368c84/pone.0299402.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf20/10956866/f01a82957476/pone.0299402.g004.jpg

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