Quantitative Single-Cell mRNA Analysis in Hydrogel Beads

Angew Chem Int Ed Engl. 2016 Jun 1;55(23):6698-701. doi: 10.1002/anie.201601969. Epub 2016 Apr 14.

Abstract

In recent years, technologies capable of analyzing single cells have emerged that are transforming many fields of biological research. Herein we report how DNA-functionalized hydrogel beads can serve as a matrix to capture mRNA from lysed single cells. mRNA quantification free of pre-amplification bias is ensured by using padlock probes and rolling circle amplification followed by hybridization with fluorescent probes. The number of transcripts in individual cells is assessed by simply counting fluorescent dots inside gel beads. The method extends the potential of existing techniques and provides a general platform for capturing molecules of interest from single cells.

Keywords: droplet microfluidics; gels; mRNA; rolling circle amplification; single-cell analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • DNA Primers / chemistry
  • DNA Primers / metabolism
  • Fluorescent Dyes / chemistry
  • Humans
  • Hydrogels / chemistry*
  • K562 Cells
  • Nucleic Acid Amplification Techniques*
  • Nucleic Acid Hybridization
  • Oligonucleotides / chemistry
  • Proto-Oncogene Proteins c-myc / genetics
  • RNA, Messenger / analysis*
  • Single-Cell Analysis

Substances

  • Actins
  • DNA Primers
  • Fluorescent Dyes
  • Hydrogels
  • Oligonucleotides
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • locked nucleic acid