聚丙烯酰胺
下降(电信)
有孔小珠
限制
纳米技术
二硫苏糖醇
微流控
材料科学
色谱法
化学
生物
分子生物学
计算机科学
生物化学
酶
复合材料
工程类
机械工程
电信
作者
Yongcheng Wang,Ting Cao,Jina Ko,Yinan Shen,Will Zong,Kuanwei Sheng,Wenjian Cao,Sijie Sun,Li‐Heng Cai,Ying‐Lin Zhou,Xin‐Xiang Zhang,Chenghang Zong,Ralph Weissleder,David A. Weitz
标识
DOI:10.1002/advs.201903463
摘要
Abstract Droplet‐based single cell sequencing technologies, such as inDrop, Drop‐seq, and 10X Genomics, are catalyzing a revolution in the understanding of biology. Barcoding beads are key components for these technologies. What is limiting today are barcoding beads that are easy to fabricate, can efficiently deliver primers into drops, and thus achieve high detection efficiency. Here, this work reports an approach to fabricate dissolvable polyacrylamide beads, by crosslinking acrylamide with disulfide bridges that can be cleaved with dithiothreitol. The beads can be rapidly dissolved in drops and release DNA barcode primers. The dissolvable beads are easy to synthesize, and the primer cost for the beads is significantly lower than that for the previous barcoding beads. Furthermore, the dissolvable beads can be loaded into drops with >95% loading efficiency of a single bead per drop and the dissolution of beads does not influence reverse transcription or the polymerase chain reaction (PCR) in drops. Based on this approach, the dissolvable beads are used for single cell RNA and protein analysis.
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