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Quantifying E. coli proteome and transcriptome with single-molecule sensitivity in single cells.

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TLDR
System-wide analyses of protein and mRNA expression in individual cells with single-molecule sensitivity using a newly constructed yellow fluorescent protein fusion library for Escherichia coli found that almost all protein number distributions can be described by the gamma distribution with two fitting parameters which, at low expression levels, have clear physical interpretations as the transcription rate and protein burst size.
Abstract
Protein and messenger RNA (mRNA) copy numbers vary from cell to cell in isogenic bacterial populations. However, these molecules often exist in low copy numbers and are difficult to detect in single cells. We carried out quantitative system-wide analyses of protein and mRNA expression in individual cells with single-molecule sensitivity using a newly constructed yellow fluorescent protein fusion library for Escherichia coli. We found that almost all protein number distributions can be described by the gamma distribution with two fitting parameters which, at low expression levels, have clear physical interpretations as the transcription rate and protein burst size. At high expression levels, the distributions are dominated by extrinsic noise. We found that a single cell's protein and mRNA copy numbers for any given gene are uncorrelated.

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Mixture distributions in a stochastic gene expression model with delayed feedback: a WKB approximation approach

TL;DR: A mathematical model with bursty production of protein, a one-step production delay, and feedback in the frequency of bursts is considered, focusing on examining the steady-state behaviour of the model in the slow-activation (i.e. large-delay) regime.
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Genome-wide differential gene expression in immortalized DF-1 chicken embryo fibroblast cell line

TL;DR: Bioinformatic analyses suggested that DF-1 cells were characterized by enhanced molecular mechanisms for cell cycle progression and proliferation, suppressing cell death pathways, altered cellular morphogenesis, and accelerated capacity for molecule transport.
Journal ArticleDOI

Computation of steady-state probability distributions in stochastic models of cellular networks.

TL;DR: Inventions in stochastic modeling coupled with approaches to modeling intrinsic noise via solution of the chemical master equation are described and it is shown how these techniques can be combined in a streamlined procedure for evaluation of different sources of variability in a biochemical network.
Journal ArticleDOI

Illuminating Messengers: An Update and Outlook on RNA Visualization in Bacteria.

TL;DR: An overview will be given of fluorescent techniques that can be used to reveal specific RNA molecules inside fixed and living single bacterial cells, including a critical evaluation of their caveats as well as potential solutions.
Journal ArticleDOI

Enhanced single-particle brightness and photostability of semiconductor polymer dots by enzymatic oxygen scavenging system

TL;DR: This study provides a promising approach for enhancing photostability of Pdots in long term single-particle tracking by using an efficient enzymatic oxygen scavenging system (OSS).
References
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疟原虫var基因转换速率变化导致抗原变异[英]/Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

宁北芳, +1 more
TL;DR: PfPMP1)与感染红细胞、树突状组胞以及胎盘的单个或多个受体作用,在黏附及免疫逃避中起关键的作�ly.
Journal ArticleDOI

Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection.

TL;DR: These mutants—the ‘Keio collection’—provide a new resource not only for systematic analyses of unknown gene functions and gene regulatory networks but also for genome‐wide testing of mutational effects in a common strain background, E. coli K‐12 BW25113.
Journal ArticleDOI

Stochastic Gene Expression in a Single Cell

TL;DR: This work constructed strains of Escherichia coli that enable detection of noise and discrimination between the two mechanisms by which it is generated and reveals how low intracellular copy numbers of molecules can fundamentally limit the precision of gene regulation.
Journal ArticleDOI

Global analysis of protein localization in budding yeast

TL;DR: The construction and analysis of a collection of yeast strains expressing full-length, chromosomally tagged green fluorescent protein fusion proteins helps reveal the logic of transcriptional co-regulation, and provides a comprehensive view of interactions within and between organelles in eukaryotic cells.
Journal ArticleDOI

Fabrication of microfluidic systems in poly(dimethylsiloxane)

TL;DR: Fabrication of microfluidic devices in poly(dimethylsiloxane) (PDMS) by soft lithography provides faster, less expensive routes to devices that handle aqueous solutions.
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