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Updated: Jul 19, 2026

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Determination of Plasma Membrane Partitioning for Peripherally-associated Proteins
Published on: June 15, 2018
Insights into a plasma membrane signature
1Program on Cell Adhesion, Cancer Research Center, The Burnham Institute, La Jolla, California 92037, USA.
Physiological Genomics
|April 4, 2001
Summary
This study compared plasma membrane (PM) proteomes in fibroblasts and mammary carcinoma cells. It identified common, lineage-linked, and unique proteins, revealing potential drivers of unique cell behaviors and metastatic phenotypes.
Area of Science:
- Cell Biology
- Proteomics
- Cancer Research
Background:
- The plasma membrane (PM) acts as a crucial barrier and communication hub.
- Fundamental questions about PM protein expression diversity remain unanswered.
- Understanding PM proteome variability is key to cell function and disease.
Purpose of the Study:
- To compare plasma membrane proteomes of fibroblasts and mammary carcinoma cells.
- To identify commonalities and differences in PM protein expression.
- To investigate proteins associated with the metastatic phenotype.
Main Methods:
- Proteomic analysis of plasma membranes.
- Comparative analysis of protein expression profiles.
- Identification of cell-line-specific proteins.
Main Results:
- Identified three distinct sets of PM proteins: common, lineage-linked, and unique.
- A significant portion of PM proteins (~40%) are linked to cell lineage.
- Discovered unique proteins in metastatic MDA-MB-435 cells, involved in adhesion, translation, and oxidative stress control.
Conclusions:
- Plasma membrane protein composition varies significantly between cell types.
- Unique PM proteins likely dictate specific cell behaviors and phenotypes.
- Proteins identified in metastatic cells offer potential targets for understanding metastasis.
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