PLOCHBERGER, B., T. SYCH, F. WEBER, Jiří NOVÁČEK, M. AXMANN, H. STANGL and E. SEZGIN. Lipoprotein Particles Interact with Membranes and Transfer Their Cargo without Receptors. Biochemistry. Washington: American Chemical Society, 2020, vol. 59, No 45, p. 4421-4428. ISSN 0006-2960. Available from: https://dx.doi.org/10.1021/acs.biochem.0c00748.
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Basic information
Original name Lipoprotein Particles Interact with Membranes and Transfer Their Cargo without Receptors
Authors PLOCHBERGER, B., T. SYCH, F. WEBER, Jiří NOVÁČEK (203 Czech Republic, guarantor, belonging to the institution), M. AXMANN, H. STANGL and E. SEZGIN.
Edition Biochemistry, Washington, American Chemical Society, 2020, 0006-2960.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.162
RIV identification code RIV/00216224:14740/20:00118331
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1021/acs.biochem.0c00748
UT WoS 000592835200010
Keywords in English CHOLESTEROL
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 4/3/2021 16:37.
Abstract
Lipid transfer from lipoprotein particles to cells is essential for lipid homeostasis. High-density lipoprotein (HDL) particles are mainly captured by cell membrane-associated scavenger receptor class B type 1 (SR-B1) from the bloodstream, while low-density and very-low-density lipoprotein (LDL and VLDL, respectively) particles are mostly taken up by receptor-mediated endocytosis. However, the role of the target lipid membrane itself in the transfer process has been largely neglected so far. Here, we study how lipoprotein particles (HDL, LDL, and VLDL) interact with synthetic lipid bilayers and cell-derived membranes and transfer their cargo subsequently. Employing cryoelectron microscopy, spectral imaging, and fluorescence (cross correlation spectroscopy allowed us to observe integration of all major types of lipoprotein particles into the membrane and delivery of their cargo in a receptor-independent manner. Importantly, the biophysical properties of the target cell membranes change upon delivery of cargo. The concept of receptor-independent interaction of lipoprotein particles with membranes helps us to better understand lipoprotein particle biology and can be exploited for novel treatments of dyslipidemia diseases.
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