Evidence map›Paper›PMID 25793886›Full record

ArticlePloS one2015

A model of lipid-free apolipoprotein A-I revealed by iterative molecular dynamics simulation.

Xing Zhang, Dongsheng Lei, Lei Zhang, Matthew Rames, Shengli Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
1.3field-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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

5 authors at 2 institutions in 2 countries.

Xing ZhangDepartment of Applied Physics, Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China; Molecular Foundry, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Dongsheng LeiDepartment of Applied Physics, Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China; Molecular Foundry, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Lei ZhangMolecular Foundry, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Matthew RamesMolecular Foundry, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Shengli ZhangDepartment of Applied Physics, Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China.
Xi'an Jiaotong University · CNLawrence Berkeley National Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apolipoprotein A-I (apo A-I), the major protein component of high-density lipoprotein, has been proven inversely correlated to cardiovascular risk in past decades. The lipid-free state of apo A-I is the initial stage which binds to lipids forming high-density lipoprotein. Molecular models of lipid-free apo A-I have been reported by methods like X-ray crystallography and chemical cross-linking/mass spectrometry (CCL/MS). Through structural analysis we found that those current models had limited consistency with other experimental results, such as those from hydrogen exchange with mass spectrometry. Through molecular dynamics simulations, we also found those models could not reach a stable equilibrium state. Therefore, by integrating various experimental results, we proposed a new structural model for lipid-free apo A-I, which contains a bundled four-helix N-terminal domain (1-192) that forms a variable hydrophobic groove and a mobile short hairpin C-terminal domain (193-243). This model exhibits an equilibrium state through molecular dynamics simulation and is consistent with most of the experimental results known from CCL/MS on lysine pairs, fluorescence resonance energy transfer and hydrogen exchange. This solution-state lipid-free apo A-I model may elucidate the possible conformational transitions of apo A-I binding with lipids in high-density lipoprotein formation.

Indexed as

Molecular Dynamics SimulationApolipoprotein A-ICross-Linking ReagentsHumansLipidsMass SpectrometryProtein Structure, SecondaryAPOA1 protein, humanApolipoprotein A-ICross-Linking ReagentsLipids

Identifiers

PMID25793886
PMCPMC4368682
OpenAlexW2034357556

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.