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Related Concept Videos

Proteomics01:33

Proteomics

7.2K
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...
7.2K

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Related Experiment Video

Updated: Jun 2, 2025

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
10:37

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification

Published on: November 15, 2017

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Robust collection and processing for label-free single voxel proteomics.

Reta Birhanu Kitata1, Marija Velickovic2, Zhangyang Xu1

  • 1Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.

Nature Communications
|January 13, 2025
PubMed
Summary
This summary is machine-generated.

A new method called Surfactant-assisted One-Pot voxel processing (wcSOP) enables robust single voxel proteomics. This technique allows for detailed spatial proteome mapping of tissue microenvironments, revealing region-specific protein signatures.

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Related Experiment Videos

Last Updated: Jun 2, 2025

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Area of Science:

  • Proteomics
  • Biotechnology
  • Tissue Microenvironment Analysis

Background:

  • Bulk tissue proteomics lacks spatial resolution, obscuring cellular heterogeneity.
  • Mapping tissue microenvironments requires methods with high spatial resolution.

Purpose of the Study:

  • To develop a robust method for label-free single voxel proteomics.
  • To enable spatial proteome mapping of tissue microenvironments.

Main Methods:

  • Integrated wet collection of single microscale tissue voxels.
  • Surfactant-assisted One-Pot voxel processing (wcSOP) method.
  • Laser capture microdissection (LCM) for voxel isolation.

Main Results:

  • Reproducible quantification of ~900 proteins from 20µm voxels (~1 cell region).
  • Quantification of ~4600 proteins from 200µm voxels (~100 cell region).
  • Demonstrated applicability to fresh frozen, OCT-embedded, and FFPE human tissues.

Conclusions:

  • wcSOP enables robust, label-free single voxel proteomics.
  • The method reveals spatially resolved protein signatures and signaling pathways.
  • wcSOP-MS facilitates routine spatial proteomics and tissue microenvironment analysis.