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InTraSeq:一种揭示新的单细胞生物学和调控机制的多模态检测方法。

InTraSeq: A Multimodal Assay that Uncovers New Single-Cell Biology and Regulatory Mechanisms.

作者信息

Beausoleil Sean, Ariss Majd, Huang Linglin, Ding Xiaokai, Sheth Shivani, Levy Tyler, Fisher Jeremy, Loebelenz Jean, Arlotta Keith, Dixon Karen, Polakiewicz Roberto, Kuchroo Vijay

机构信息

Cell Signaling Technology, Inc., Danvers, Massachusetts, USA.

The Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Res Sq. 2024 Dec 9:rs.3.rs-5284652. doi: 10.21203/rs.3.rs-5284652/v1.

Abstract

Single-cell RNA sequencing (scRNA-seq) has revolutionized cell biology by enabling the profiling of transcriptomes at a single-cell resolution, leading to important discoveries that have advanced our understanding of cellular and tissue heterogeneity, developmental trajectories, and disease progression. Despite these important advances, scRNA-seq is limited to measuring the transcriptome providing a partial view of cellular function. To address this limitation, multimodal scRNA-seq assays have emerged, allowing for the simultaneous measurement of RNA expression and protein. Intracellular Transcriptomic and Protein Sequencing (InTraSeq), a novel multimodal scRNA-seq technology described here, enables the concurrent measurement of mRNA, surface markers, cytoplasmic proteins, and nuclear proteins within individual cells through oligo-barcoded antibodies. This method offers a comprehensive approach to studying cellular function by combining RNA and protein pro ling from the same sample and utilizing a relatively simple protocol. The InTraSeq method enables researchers to expand their view of critical intracellular protein expression including post-translational modifications (PTMs) and transcription factors, allowing for the identification of novel cellular subtypes and states that may be obscured by RNA-based analyses alone. This is particularly valuable in understanding the heterogeneity of cell populations and identifying distinct functional states. In this report, we used InTraSeq to characterize the complex cellular states and regulatory mechanisms during Th17 cell differentiation. We simultaneously pro led RNA and protein expression in over 85,000 cells, capturing transcriptional changes, changes in protein expression and the dynamics of signaling pathways at a high resolution. Our results revealed novel insights into Th17 cell differentiation, including the identification of key regulatory factors and their target genes. By simultaneously measuring mRNA, extra and intra-cellular proteins, signaling proteins, and PTMs, InTraSeq offers a comprehensive understanding of cellular processes and enables the identification of novel regulatory mechanisms.

摘要

单细胞RNA测序(scRNA-seq)通过实现单细胞分辨率下的转录组分析,彻底改变了细胞生物学,带来了重要发现,推动了我们对细胞和组织异质性、发育轨迹及疾病进展的理解。尽管取得了这些重要进展,但scRNA-seq仅限于测量转录组,只能提供细胞功能的部分视图。为解决这一局限性,多模态scRNA-seq检测方法应运而生,可同时测量RNA表达和蛋白质。本文介绍的一种新型多模态scRNA-seq技术——细胞内转录组学和蛋白质测序(InTraSeq),能够通过寡核苷酸条形码抗体同时测量单个细胞内的mRNA、表面标志物、细胞质蛋白和核蛋白。该方法通过结合来自同一样本的RNA和蛋白质分析,并采用相对简单的方案,提供了一种全面研究细胞功能的方法。InTraSeq方法使研究人员能够扩展对关键细胞内蛋白质表达的认识,包括翻译后修饰(PTM)和转录因子,从而识别可能仅通过基于RNA的分析而被掩盖的新型细胞亚型和状态。这对于理解细胞群体的异质性和识别不同的功能状态尤为有价值。在本报告中,我们使用InTraSeq来表征Th17细胞分化过程中的复杂细胞状态和调控机制。我们同时分析了超过85000个细胞中的RNA和蛋白质表达,以高分辨率捕捉转录变化、蛋白质表达变化和信号通路动态。我们的结果揭示了Th17细胞分化的新见解,包括关键调控因子及其靶基因的鉴定。通过同时测量mRNA、细胞外和细胞内蛋白质、信号蛋白和PTM,InTraSeq提供了对细胞过程的全面理解,并能够识别新的调控机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2170/11661302/e02fc2570eb9/nihpp-rs5284652v1-f0001.jpg

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