Evidence map›Paper›PMID 29564446›Full record

ArticleNanoscale2018

Lipid composition dictates serum stability of reconstituted high-density lipoproteins: implications for in vivo applications.

Sean F Gilmore, Timothy S Carpenter, Helgi I Ingólfsson, Sandra K G Peters, Paul T Henderson, Craig D Blanchette, Nicholas O Fischer

Open access · greenAbstract read
In one paragraph

Article in Nanoscale, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Advances in HDL: Much More than Lipid Transporters.International journal of molecular sciences · 2020
    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 2 institutions in 1 country.

Sean F GilmoreLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.ORCID http://orcid.org/0000-0002-7917-1413
Timothy S CarpenterLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.ORCID http://orcid.org/0000-0001-7848-9983
Helgi I IngólfssonLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.ORCID http://orcid.org/0000-0002-7613-9143
Sandra K G PetersLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.
Paul T HendersonUniversity of California-Davis (UC Davis) and UC Davis Comprehensive Cancer Center, Sacramento, California 95817, USA.
Craig D BlanchetteLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.
Nicholas O FischerLawrence Livermore National Laboratory, Livermore, CA 94550, USA. fischer29@llnl.gov.
Lawrence Livermore National Laboratory · USUC Davis Comprehensive Cancer Center

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
NCI NIH HHS P30 CA093373
6 · The paper itself

Abstract

Nanolipoprotein particles (NLPs) are reconstituted high-density lipoproteins, consisting of a phospholipid bilayer stabilized by an apolipoprotein scaffold protein. This class of nanoparticle has been a vital tool in the study of membrane proteins, and in recent years has been increasingly used for in vivo applications. Previous work demonstrated that the composition of the lipid bilayer component affects the stability of these particles in serum solutions. In the current study, NLPs assembled with phosphatidylcholine lipids featuring different acyl chain structures were systematically tested to understand the effect that lipid composition has on NLP stability in both neat serum and cell culture media supplemented with 10% serum by volume. The time at which 50% of the particles dissociate, as well as the fraction of the initial population that remains resistant to dissociation, were correlated to key parameters obtained from all-atom simulations of the corresponding lipid bilayers. A significant correlation was observed between the compressibility modulus of the lipid bilayer and particle stability in these complex biological milieu. These results can be used as a reference to tune the stability of these versatile biological nanoparticles for in vitro and in vivo applications.

Indexed as

ApolipoproteinsLipid BilayersLipoproteins, HDLMolecular Dynamics SimulationNanoparticlesPhosphatidylcholinesProtein StabilityApolipoproteinsLipid BilayersLipoproteins, HDLPhosphatidylcholines

Identifiers

PMID29564446
PMCPMC7485573
OpenAlexW2793033156

What OpenQuestion holds

Textmetadata
LicenceTDM
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.