Please use this identifier to cite or link to this item:
doi:10.22028/D291-39000
Title: | Bilayer-Embedded Lipid Droplets Coated with Perilipin-2 Display a Pancake Shape |
Author(s): | Puza, Sevde Asfia, Shima Seemann, Ralf Fleury, Jean-Baptiste |
Language: | English |
Title: | International Journal of Molecular Sciences |
Volume: | 24 |
Issue: | 3 |
Publisher/Platform: | MDPI |
Year of Publication: | 2023 |
Free key words: | lipid droplet diffusion FRAP phospholipid ADRP |
DDC notations: | 500 Science |
Publikation type: | Journal Article |
Abstract: | Lipid droplets (LD) are organelles localized in the membrane of the endoplasmic reticulum (ER) that play an important role in many biological functions. Free LDs that have been released from the ER membrane and are present in the cytosol resemble an oil-in-water emulsion. The surface of an LD is coated with a phospholipid monolayer, and the core of an LD is composed of neutral lipids. Adipose differentiation-related protein (ADRP), also known as perilipin-2, is a protein that surrounds the LD, together with the phospholipid monolayer. ADRP molecules are involved in assisting in the storage of neutral lipids within LDs. In this article, we focus our interest on the influence of ADRP molecules on the 3D shape of bilayer-embedded LDs and the diffusion of phospholipids in the monolayer covering LDs. For this study, we employed two different microfluidic setups: one to produce and explore bilayer-embedded LDs and a second one to mimic the surface of a single LD. Using the first setup, we demonstrate that ADRP molecules stay preferentially localized on the surfaces of bilayer-embedded LDs, and we study their 3D-shape in the presence of ADRP. Using the second setup, we performed FRAP experiments to measure the phospholipid diffusion on a model LD surface as a function of the ADRP concentration. Although the presence of proteins on the LD surface minimally affects the phospholipid and protein motility, ADRP appears to have a significant effect on the 3D structure of LDs embedded in the bilayer. |
DOI of the first publication: | 10.3390/ijms24032072 |
URL of the first publication: | https://doi.org/10.3390/ijms24032072 |
Link to this record: | urn:nbn:de:bsz:291--ds-390004 hdl:20.500.11880/35175 http://dx.doi.org/10.22028/D291-39000 |
ISSN: | 1422-0067 |
Date of registration: | 13-Feb-2023 |
Description of the related object: | Supplementary Materials |
Related object: | https://www.mdpi.com/article/10.3390/ijms24032072/s1 |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Physik |
Professorship: | NT - Prof. Dr. Ralf Seemann |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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ijms-24-02072.pdf | 678,69 kB | Adobe PDF | View/Open |
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