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Related Concept Videos

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...

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Related Experiment Video

Updated: May 30, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
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MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method

Published on: October 7, 2025

Quantitative proteomics identify novel miR-155 target proteins.

Christopher Lössner1, Jan Meier, Uwe Warnken

  • 1Functional Proteome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Plos One
|July 30, 2011
PubMed
Summary

Researchers identified 46 potential target proteins for microRNA miR-155 using SILAC proteomics. This study reveals miR-155

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Area of Science:

  • Molecular Biology
  • Genetics
  • Proteomics

Background:

  • MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression.
  • Dysregulation of miR-155 is implicated in various diseases, including cancer.
  • Understanding miRNA targets is crucial for elucidating their biological roles.

Purpose of the Study:

  • To identify novel protein targets of miR-155.
  • To investigate the functional implications of miR-155 targeting.
  • To assess the cell-line specificity of miRNA targets.

Main Methods:

  • Stable Isotope Labeling by Amino acids in cell culture (SILAC) for quantitative proteomics.
  • Luciferase reporter assays to validate miRNA-target interactions.
  • Bioinformatic analysis for functional annotation of identified targets.

Main Results:

  • Identified 46 putative protein targets of miR-155.
  • Confirmed CKAP5 as a novel miR-155 target using luciferase assays.
  • Functional annotation suggests a role for miR-155 targets in cell cycle regulation.

Conclusions:

  • This study presents the first large-scale investigation of miR-155 targets in HEK293T cells.
  • Findings highlight the cell-specific nature of microRNA targeting.
  • Identified targets provide insights into miR-155's role in cellular processes.