Evidence mapPaperPMID 41459334Full record

ArticleBiochemistry and biophysics reports2026

Influence of PLIN5 and lipid composition on lipid droplet contact sites with other organelles.

Mahsa Mohammadian, Shima Asfia, Ralf Seemann

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Article in Biochemistry and biophysics reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mahsa MohammadianDepartment of Experimental Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany.
Shima AsfiaDepartment of Experimental Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany.
Ralf SeemannDepartment of Experimental Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid droplets (LDs) maintain cellular lipid homeostasis through dynamic interactions with other organelles. Understanding how these contact sites form is crucial for uncovering the mechanisms of lipid exchange and signaling. In this study, we used an in vitro model to investigate how lipid composition and the LD-associated protein perilipin 5 (PLIN5) influence contact formation between an LD monolayer and a bilayer membrane. Artificial LDs consisting of triolein and coated with either a DOPE or DOPC monolayer containing PLIN5 or not were incubated with large unilamellar vesicles (LUVs) that mimic the bilayer membrane of the organelle. Using double fluorescence labeling of the LUV bilayer and the core, we can distinguish between fusion of the LUV bilayer with the LDs and stable attachment of LUVs to the LD's surface. Our results show that the probability of fusion between LDs and LUVs is greatly increased for DOPE-coated LDs, while PLIN5 promotes the stable attachment of LUVs to the LD's surface and prevents fusion. These observations illustrate how certain lipid and protein components can modulate contact formation between LDs and membranes in a controlled in vitro system, and provide a basis for future studies on the molecular mechanisms of organelle communication.

Indexed as

Contact siteLarge unilamellar vesicleLipid dropletLipidic bridgePerilipin 5PLIN5Protein tether

Identifiers

PMID41459334
PMCPMC12743417

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.