Evidence map›Paper›PMID 33147967›Full record

ArticleBiochemistry2020

Lipoprotein Particles Interact with Membranes and Transfer Their Cargo without Receptors.

Birgit Plochberger, Taras Sych, Florian Weber, Jiri Novacek, Markus Axmann, Herbert Stangl, Erdinc Sezgin

Open access · hybridAbstract read
In one paragraph

Article in Biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  10. Review
  11. Apolipoprotein E and Atherosclerosis.Current atherosclerosis reports · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 4 countries.

Birgit PlochbergerTU Wien, Institute of Applied Physics, Vienna 1040, Austria.ORCID 0000-0003-2733-9947
Taras SychScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, 17165 Solna, Sweden.
Florian WeberUpper Austria University of Applied Sciences, Campus Linz, Linz 4020, Austria.
Jiri NovacekCEITEC, Masaryk University, University Campus Bohunice, Brno 62500, Czech Republic.
Markus AxmannMedical University of Vienna, Center for Pathobiochemistry and Genetics, Institute of Medical Chemistry, Vienna 1090, Austria.
Herbert StanglMedical University of Vienna, Center for Pathobiochemistry and Genetics, Institute of Medical Chemistry, Vienna 1090, Austria.
Erdinc SezginScience for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, 17165 Solna, Sweden.ORCID 0000-0002-4915-388X
Science for Life Laboratory · SEMedical University of Vienna · ATJohannes Kepler University of Linz · ATMasaryk University · CZ

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G0902418Medical Research Council MC_UU_12010Medical Research Council MC_UU_12025Medical Research Council MR/K01577X/1Wellcome Trust 104924/14/Z/14
6 · The paper itself

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 cryo-electron 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.

Indexed as

Biological TransportCell MembraneLipid BilayersLipoproteinsMicroscopy, Atomic ForceLipid BilayersLipoproteins

Identifiers

PMID33147967
PMCPMC7677925
OpenAlexW3081811044

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.