Multiplexed detection of RNA using MERFISH and branched DNA amplification

被引:0
|
作者
Chenglong Xia
Hazen P. Babcock
Jeffrey R. Moffitt
Xiaowei Zhuang
机构
[1] Howard Hughes Medical Institute,Center for Advanced Imaging
[2] Department of Chemistry and Chemical Biology,undefined
[3] and Department of Physics,undefined
[4] Harvard University,undefined
[5] Harvard University,undefined
[6] Program in Cellular and Molecular Medicine,undefined
[7] Boston Children’s Hospital; Department of Microbiology,undefined
[8] Harvard Medical School,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Multiplexed error-robust fluorescence in situ hybridization (MERFISH) allows simultaneous imaging of numerous RNA species in their native cellular environment and hence spatially resolved single-cell transcriptomic measurements. However, the relatively modest brightness of signals from single RNA molecules can become limiting in a number of applications, such as increasing the imaging throughput, imaging shorter RNAs, and imaging samples with high degrees of background, such as some tissue samples. Here, we report a branched DNA (bDNA) amplification approach for MERFISH measurements. This approach produces a drastic signal increase in RNA FISH samples without increasing the fluorescent spot size for individual RNAs or increasing the variation in brightness from spot to spot, properties that are important for MERFISH imaging. Using this amplification approach in combination with MERFISH, we demonstrated RNA imaging and profiling with a near 100% detection efficiency. We further demonstrated that signal amplification improves MERFISH performance when fewer FISH probes are used for each RNA species, which should allow shorter RNAs to be imaged. We anticipate that the combination of bDNA amplification with MERFISH should facilitate many other applications and extend the range of biological questions that can be addressed by this technique in both cell culture and tissues.
引用
收藏
相关论文
共 50 条
  • [1] Multiplexed detection of RNA using MERFISH and branched DNA amplification
    Xia, Chenglong
    Babcock, Hazen P.
    Moffitt, Jeffrey R.
    Zhuang, Xiaowei
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [2] Ultrasensitive detection of HIV DNA using an electrochemical biosensor with branched DNA amplification
    Ma, Mingyi
    He, Li
    Shi, Xiaoxue
    Wang, Yanchao
    Hai, Hong
    Wei, Xiaoping
    INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE, 2023, 18 (10):
  • [3] Multiplexed detection of pathogenic DNA using zinc finger proteins without DNA amplification
    Kim, Juhwa
    Kim, Moon-Soo
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [4] EVALUATION OF BRANCHED DNA SIGNAL AMPLIFICATION FOR THE DETECTION OF HEPATITIS-C VIRUS-RNA
    ALTER, HJ
    SANCHEZPESCADOR, R
    URDEA, MS
    WILBER, JC
    LAGIER, RJ
    DIBISCEGLIE, AM
    SHIH, JW
    NEUWALD, PD
    JOURNAL OF VIRAL HEPATITIS, 1995, 2 (03) : 121 - 132
  • [5] RNA Imaging with Multiplexed Error-Robust Fluorescence In Situ Hybridization (MERFISH)
    Moffitt, J. R.
    Zhuang, X.
    VISUALIZING RNA DYNAMICS IN THE CELL, 2016, 572 : 1 - 49
  • [7] DIRECT AND QUANTITATIVE DETECTION OF HIV-1 RNA IN HUMAN PLASMA WITH A BRANCHED DNA SIGNAL AMPLIFICATION ASSAY
    URDEA, MS
    WILBER, JC
    YEGHIAZARIAN, T
    TODD, JA
    KERN, DG
    FONG, SJ
    BESEMER, D
    HOO, B
    SHERIDAN, PJ
    KOKKA, R
    NEUWALD, P
    PACHL, CA
    AIDS, 1993, 7 : S11 - S14
  • [8] QUANTITATION OF HIV-1 RNA IN PLASMA USING A SIGNAL AMPLIFICATION BRANCHED DNA (BDNA) ASSAY
    PACHL, C
    ELBEIK, T
    SAXER, M
    KERN, D
    STEMPEIN, M
    FONG, SJ
    SHERIDAN, P
    YEGHIAZARIAN, T
    NEUWALD, P
    URDEA, M
    FEINBERG, M
    TODD, J
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 20 - 20
  • [9] BRANCHED DNA SIGNAL AMPLIFICATION
    URDEA, MS
    BIO-TECHNOLOGY, 1994, 12 (09): : 926 - 928