Evidence map›Paper›PMID 24988346›Full record

ArticleBiophysical journal2014

The orientation and dynamics of estradiol and estradiol oleate in lipid membranes and HDL disc models.

Alexander Vogel, Holger A Scheidt, Scott E Feller, Jari Metso, Robert M Badeau, Matti J Tikkanen, Kristiina Wähälä, Matti Jauhiainen, Daniel Huster

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

9 authors at 6 institutions in 4 countries.

Alexander VogelInstitute of Medical Physics and Biophysics, University of Leipzig, Leipzig, Germany.
Holger A ScheidtInstitute of Medical Physics and Biophysics, University of Leipzig, Leipzig, Germany.
Scott E FellerWabash College, Crawfordsville, Indiana.
Jari MetsoNational Institute for Health and Welfare, Public Health Genomics Unit and Institute for Molecular Medicine Finland, Helsinki, Finland.
Robert M BadeauTurku Positron Emission Tomography Centre, University of Turku, Turku, Finland.
Matti J TikkanenFolkälsan Research Center, Biomedicum and Heart and Lung Center, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland.
Kristiina WähäläLaboratory of Organic Chemistry, University of Helsinki, Helsinki, Finland.
Matti JauhiainenNational Institute for Health and Welfare, Public Health Genomics Unit and Institute for Molecular Medicine Finland, Helsinki, Finland.
Daniel HusterInstitute of Medical Physics and Biophysics, University of Leipzig, Leipzig, Germany; Department of Chemical Sciences, Tata Institute of Fundamental Research, Mumbai, India. Electronic address: daniel.huster@medizin.uni-leipzig.de.
Institute for Molecular Medicine Finland · FILeipzig University · DEUniversity of Helsinki · FITata Institute of Fundamental Research · INUniversity of Turku · FIWabash College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estradiol (E2) and E2 oleate associate with high-density lipoproteins (HDLs). Their orientation in HDLs is unknown. We studied the orientation of E2 and E2 oleate in membranes and reconstituted HDLs, finding that E2 and E2 oleate are membrane-associated and highly mobile. Our combination of NMR measurements, molecular dynamics simulation, and analytic theory identifies three major conformations where the long axis of E2 assumes a parallel, perpendicular, or antiparallel orientation relative to the membrane's z-direction. The perpendicular orientation is preferred, and furthermore, in this orientation, E2 strongly favors a particular roll angle, facing the membrane with carbons 6, 7, 15, and 16, whereas carbons 1, 2, 11, and 12 point toward the aqueous phase. In contrast, the long axis of E2 oleate is almost exclusively oriented at an angle of ∼60° to the z-direction. In such an orientation, the oleoyl chain is firmly inserted into the membrane. Thus, both E2 and E2 oleate have a preference for interface localization in the membrane. These orientations were also found in HDL discs, suggesting that only lipid-E2 interactions determine the localization of the molecule. The structural mapping of E2 and E2 oleate may provide a design platform for specific E2-HDL-targeted pharmacological therapies.

Indexed as

Molecular Dynamics SimulationEstradiolLipoproteins, HDLLiposomesOleic AcidEstradiolLipoproteins, HDLLiposomesOleic Acid

Identifiers

PMID24988346
PMCPMC4119277
OpenAlexW2002505077

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.