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Related Concept Videos

Ribosome Profiling02:24

Ribosome Profiling

Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
Proteomics01:33

Proteomics

A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term proteomics...
Cell Lines01:16

Cell Lines

A cell line is a population of cells grown in vitro that can be subcultured over several generations. Normal cells cease to divide after a certain number of cell divisions, a process known as replicative senescence. This number, called the Hayflick limit, was conceptualized by Leonard Hayflick in 1961 when he observed that fetal cells grown in culture could only divide 40-60 times. This limit is due to the shortening of the telomeres during each round of cell division, preventing cell division...

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Related Experiment Video

Updated: Jun 5, 2026

Cell-Lineage Guided Mass Spectrometry Proteomics in the Developing (Frog) Embryo
09:18

Cell-Lineage Guided Mass Spectrometry Proteomics in the Developing (Frog) Embryo

Published on: April 21, 2022

Defining the transcriptome and proteome in three functionally different human cell lines.

Emma Lundberg1, Linn Fagerberg, Daniel Klevebring

  • 1Science for Life Laboratory, Royal Institute of Technology, Stockholm, Sweden.

Molecular Systems Biology
|December 24, 2010
PubMed
Summary
This summary is machine-generated.

This study reveals that most gene products (>60%) are found in all human cells. While mRNA and protein levels correlate, proteins show greater abundance differences, with cell-specific proteins often being low-abundance and cell-surface located.

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TRAP-rc, Translating Ribosome Affinity Purification from Rare Cell Populations of Drosophila Embryos
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Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
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Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

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Last Updated: Jun 5, 2026

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Published on: April 21, 2022

TRAP-rc, Translating Ribosome Affinity Purification from Rare Cell Populations of Drosophila Embryos
10:26

TRAP-rc, Translating Ribosome Affinity Purification from Rare Cell Populations of Drosophila Embryos

Published on: September 10, 2015

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
12:54

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

Area of Science:

  • Human biology
  • Molecular biology
  • Cell biology

Background:

  • Understanding cell and tissue differences in gene and protein expression is crucial for delineating biological function.
  • Global analysis of mRNA and protein levels provides insights into cellular specificity.

Purpose of the Study:

  • To perform a global analysis of mRNA and protein levels in three distinct human cell lines.
  • To estimate cell-specific and shared gene/protein expression fractions.
  • To characterize transcriptome and proteome differences across human cells.

Main Methods:

  • Sequence-based transcriptome analysis (RNA-seq).
  • Stable Isotope Labeling by Amino acids in Cell culture (SILAC)-based mass spectrometry.
  • Antibody-based confocal microscopy.

Main Results:

  • Over 60% of gene products were detected in all cell lines, indicating ubiquitous RNA expression.
  • High correlations were observed between mRNA and protein level changes, despite proteins having a wider dynamic range.
  • Cell-type specific proteins were generally low in abundance and enriched in cell-surface proteins.

Conclusions:

  • The study provides a comprehensive method for characterizing the transcriptome and proteome in human cells.
  • Cellular specificity is largely defined by the abundance and localization of proteins, particularly cell-surface proteins.