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Easy and Accessible Workflow for Label-Free Single-Cell Proteomics.

JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY(2023)

Brigham Young Univ

Cited 15|Views26
Abstract
Single-cell proteomics (SCP) can provide information that is unattainable through either bulk-scale protein measurements or single-cell profiling of other omes. Maximizing proteome coverage often requires custom instrumentation, consumables, and reagents for sample processing and separations, which has limited the accessibility of SCP to a small number of specialized laboratories. Commercial platforms have become available for SCP cell isolation and sample preparation, but the high cost of these platforms and the technical expertise required for their operation place them out of reach of many interested laboratories. Here, we assessed the new HP D100 Single Cell Dispenser for label-free SCP. The low-cost instrument proved highly accurate and reproducible for dispensing reagents in the range from 200 nL to 2 μL. We used the HP D100 to isolate and prepare single cells for SCP within 384-well PCR plates. When the well plates were immediately centrifuged following cell dispensing and again after reagent dispensing, we found that ∼97% of wells that were identified in the instrument software as containing a single cell indeed provided the proteome coverage expected of a single cell. This commercial dispenser combined with one-step sample processing provides a very rapid and easy-to-use workflow for SCP with no reduction in proteome coverage relative to a nanowell-based workflow, and the commercial well plates also facilitate autosampling with unmodified instrumentation. Single-cell samples were analyzed using home-packed 30 μm i.d. nanoLC columns as well as commercially available 50 μm i.d. columns. The commercial columns resulted in ∼35% fewer identified proteins. However, combined with the well plate-based preparation platform, the presented workflow provides a fully commercial and relatively low-cost alternative for SCP sample preparation and separation, which should greatly broaden the accessibility of SCP to other laboratories.
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要点】:本文介绍了一种简便、无需标记的单细胞蛋白质组学工作流程,通过一种低成本的仪器和商业化的微孔板,实现了与纳米孔基于工作流程相当的 proteome 覆盖,降低了单细胞蛋白质组学的技术门槛。

方法】:研究使用了HP D100单细胞分配器进行细胞和试剂的分配,并结合一步样品处理技术。

实验】:实验在384孔PCR板中进行单细胞分离和准备,通过软件识别包含单细胞的孔,并经过离心确认,结果显示约97%的孔确实提供了预期的蛋白质组覆盖。分析时使用了家装30μm内径的纳米LC柱和商用50μm内径的柱,结果显示商用柱鉴定的蛋白质数量减少了约35%,但与基于微孔板的制备平台结合,该工作流程提供了一种完全商业化和相对低成本的SCP样品制备和分离替代方案。