Bilayer-Embedded Lipid Droplets Coated with Perilipin-2 Display a Pancake Shape

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.

Binding of perilipin 3 to membranes containing diacylglycerol is mediated by conserved residues within its PAT domain

“…PLINs are both abundant and complex proteins that are likely important to fulfill a variety of functions, not only in regulating the access and activity of lipases but also by stabilizing the LD surface, preventing the coalescence of LDs, and promoting their formation from the ER membrane ( 32 , 41 , 62 ). Their typical three domain structure with an N-terminal PAT domain, a central 11-mer repeat AH, and a C-terminal 4-helix bundle has likely evolved to provide these functions under various physiological conditions.…”