Rao Shilpa, Tonn Tori, Cenik Can
Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA.
Methods Mol Biol. 2025;2923:197-214. doi: 10.1007/978-1-0716-4522-2_12.
Transcriptome-wide translation can be measured using ribosome profiling, a technique which relies on deep sequencing of ribosome protected fragments. This method enables comprehensive measurement of in vivo translation; however, it involves multiple steps and thereby demands high-input samples. Here, we describe Ribo-ITP (RIBOsome profiling via IsoTachoPhoresis), which utilizes the principles of isotachophoresis coupled with a stringent size selection strategy in a microfluidic chip to isolate ribosome-protected fragments. Ribo-ITP allows quantitative measurement of translation from rare populations like cancer stem cells, early embryonic stages, and other ultralow input samples including single cells.
全转录组范围的翻译可以使用核糖体图谱分析来测量,该技术依赖于对核糖体保护片段的深度测序。这种方法能够全面测量体内翻译;然而,它涉及多个步骤,因此需要高输入量的样本。在这里,我们描述了Ribo-ITP(通过等速电泳进行核糖体图谱分析),它利用等速电泳原理并结合微流控芯片中的严格大小选择策略来分离核糖体保护片段。Ribo-ITP允许对来自癌症干细胞、早期胚胎阶段等稀有群体以及包括单细胞在内的其他超低输入量样本的翻译进行定量测量。