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Endophilin recruitment drives membrane curvature generation through coincidence detection of GPCR loop interactions and negative lipid charge

Samsuzzoha Mondal, Karthik Narayan, Imania Powers, Samuel Botterbusch, Tobias Baumgart

2020Journal of Biological Chemistry14 citationsDOIOpen Access PDF

Abstract

represented by a covalently conjugated TIL region from the β1-adrenergic receptor. We observed that TIL recruits endophilin to membranes composed of 95 mol% of zwitterionic lipids via the SH3 domain. More importantly, endophilin recruited via TIL tubulates vesicles and gets sorted onto highly curved membrane tubules. These observations indicate that the cellular membrane bending and curvature sensing activities of endophilin can be facilitated through detection of the TIL of activated GPCRs in addition to binding to anionic lipids. Furthermore, we show that TIL electrostatically interacts with membranes composed of anionic lipids. Therefore, anionic lipids can modulate TIL/SH3 domain binding. Overall, our findings imply that an interplay between TIL, charged membrane lipids, BAR domain, and SH3 domain could exist in the biological system and that these components may act in coordination to regulate the internalization of cellular receptors.

Topics & Concepts

EndocytosisInternalizationMembrane curvatureG protein-coupled receptorAmphiphysinCell biologyChemistryMembraneSH3 domainReceptorLipid bilayerBiophysicsBiologyBiochemistryDynaminProto-oncogene tyrosine-protein kinase SrcLipid Membrane Structure and BehaviorCellular transport and secretionReceptor Mechanisms and Signaling
Endophilin recruitment drives membrane curvature generation through coincidence detection of GPCR loop interactions and negative lipid charge | Litcius