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Ultra-sensitive digital quantification of proteins and mRNA in single cells.


ABSTRACT: Simultaneous measurement of proteins and mRNA in single cells enables quantitative understanding and modeling of cellular functions. Here, we present an automated microfluidic system for multi-parameter and ultra-sensitive protein/mRNA measurements in single cells. Our technology improves the sensitivity of digital proximity ligation assay by up to 55-fold, with a detection limit of 2277 proteins per cell and with detection efficiency of as few as 29 protein molecules. Our measurements using this system reveal higher mRNA/protein correlation in single mammalian cells than previous estimates. Furthermore, time-lapse imaging of herpes simplex virus 1 infected epithelial cells enabled by our device shows that expression of ICP4 -a major transcription factor regulating hundreds of viral genes- is only partially correlated with viral protein counts, suggesting that many cells go through abortive infection. These results highlight the importance of high-sensitivity protein/mRNA quantification for understanding fundamental molecular mechanisms in individual cells.

SUBMITTER: Lin J 

PROVIDER: S-EPMC6685952 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Ultra-sensitive digital quantification of proteins and mRNA in single cells.

Lin Jing J   Jordi Christian C   Son Minjun M   Van Phan Hoang H   Drayman Nir N   Abasiyanik Mustafa Fatih MF   Vistain Luke L   Tu Hsiung-Lin HL   Tay Savaş S  

Nature communications 20190807 1


Simultaneous measurement of proteins and mRNA in single cells enables quantitative understanding and modeling of cellular functions. Here, we present an automated microfluidic system for multi-parameter and ultra-sensitive protein/mRNA measurements in single cells. Our technology improves the sensitivity of digital proximity ligation assay by up to 55-fold, with a detection limit of 2277 proteins per cell and with detection efficiency of as few as 29 protein molecules. Our measurements using thi  ...[more]

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