Department of Bioengineering, University of California Berkeley, Berkeley, CA, USA.
The University of California Berkeley and University of California San Francisco Graduate Program in Bioengineering, Berkeley, CA, USA.
Nat Protoc. 2021 Feb;16(2):1062-1088. doi: 10.1038/s41596-020-00449-2. Epub 2021 Jan 15.
Although mammalian embryo development depends on critical protein isoforms that arise from embryo-specific nucleic acid modifications, the role of these isoforms is not yet clear. Challenges arise in measuring protein isoforms and nucleic acids from the same single embryos and blastomeres. Here we present a multimodal technique for performing same-embryo nucleic acid and protein isoform profiling (single-embryo nucleic acid and protein profiling immunoblot, or snapBlot). The method integrates protein isoform measurement by fractionation polyacrylamide gel electrophoresis (fPAGE) with off-chip analysis of nucleic acids from the nuclei. Once embryos are harvested and cultured to the desired stage, they are sampled into the snapBlot device and subjected to fPAGE. After fPAGE, 'gel pallets' containing nuclei are excised from the snapBlot device for off-chip nucleic acid analyses. fPAGE and nuclei analyses are indexed to each starting sample, yielding same-embryo multimodal measurements. The entire protocol, including processing of samples and data analysis, takes 2-3 d. snapBlot is designed to help reveal the mechanisms by which embryo-specific nucleic acid modifications to both genomic DNA and messenger RNA orchestrate the growth and development of mammalian embryos.
尽管哺乳动物胚胎的发育依赖于从胚胎特异性核酸修饰中产生的关键蛋白异构体,但这些异构体的作用尚不清楚。从同一个胚胎和卵裂球中测量蛋白异构体和核酸会带来挑战。本文提出了一种对同一胚胎的核酸和蛋白异构体进行分析的多模式技术(单细胞胚胎核酸和蛋白分析免疫印迹或 snapBlot)。该方法将通过分级聚丙烯酰胺凝胶电泳(fPAGE)的蛋白异构体测量与芯片外的核内核酸分析相结合。一旦胚胎被收获并培养到所需的阶段,就可以将其取样到 snapBlot 设备中,并进行 fPAGE。在 fPAGE 之后,从 snapBlot 设备中切下含有核的“凝胶托盘”进行芯片外核酸分析。fPAGE 和核分析与每个起始样本相关联,从而产生同一胚胎的多模式测量。整个方案,包括样品处理和数据分析,需要 2-3 天。snapBlot 的设计旨在帮助揭示胚胎特异性核酸修饰对基因组 DNA 和信使 RNA 的作用机制,这些修饰调控着哺乳动物胚胎的生长和发育。