Evidence map›Paper›PMID 21855534›Full record

ArticleChemistry and physics of lipids2011

Using spin-label electron paramagnetic resonance (EPR) to discriminate and characterize the cholesterol bilayer domain.

Marija Raguz, Laxman Mainali, Justyna Widomska, Witold K Subczynski

Abstract read
In one paragraph

Article in Chemistry and physics of lipids, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
–field-weighted citation impact
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

57 citing papers in PubMed.

  1. Article
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  9. Interaction of βInternational journal of molecular sciences · 2023
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  10. Binding of βInternational journal of molecular sciences · 2023
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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

4 authors.

Marija RaguzDepartment of Biophysics, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Laxman Mainali
Justyna Widomska
Witold K Subczynski

Funding

TR&D Project 3P41EB001980 · NIBIB · MEDICAL COLLEGE OF WISCONSIN · PI KLUG, CANDICE S · 2003 to 2017
$16.3M
DEVELOPMENT OF BIOMEDICAL ESR INSTRUMENTATIONR01EB002052 · NIBIB · MEDICAL COLLEGE OF WISCONSIN · PI KLUG, CANDICE S · 2003 to 2015
$6.4M
Liquid Rafts in Eye Lens: Discrimination by Pulse EPRR01EY015526 · NEI · MEDICAL COLLEGE OF WISCONSIN · PI SUBCZYNSKI, WITOLD K · 2005 to 2019
$4.8M
Is Cholesterol Crystalline Domain a Barrier to Oxygen Transport in the Eye Lens?R03TW008052 · FIC · MEDICAL COLLEGE OF WISCONSIN · PI SUBCZYNSKI, WITOLD K · 2009 to 2011
$104k
FIC NIH HHS R03 TW008052FIC NIH HHS TW008052NEI NIH HHS EY015526NEI NIH HHS R01 EY015526NIBIB NIH HHS EB001980NIBIB NIH HHS EB002052NIBIB NIH HHS P41 EB001980NIBIB NIH HHS R01 EB002052
6 · The paper itself

Abstract

Electron paramagnetic resonance (EPR) spin-labeling methods make it possible not only to discriminate the cholesterol bilayer domain (CBD) but also to obtain information about the organization and dynamics of cholesterol molecules in the CBD. The abilities of spin-label EPR were demonstrated for Chol/POPC (cholesterol/1-palmitoyl-2-oleoylphosphatidylcholine) membranes, with a Chol/POPC mixing ratio that changed from 0 to 3. Using the saturation-recovery (SR) EPR approach with cholesterol analogue spin labels, ASL and CSL, and oxygen or NiEDDA relaxation agents, it was confirmed that the CBD was present in all membrane suspensions when the mixing ratio exceeded the cholesterol solubility threshold (CST). Conventional EPR spectra of ASL and CSL in the CBD were similar to those in the surrounding POPC bilayer (which is saturated with cholesterol), indicating that in both domains, cholesterol exists in the lipid-bilayer-like structures. The behavior of ASL and CSL (and, thus, the behavior of cholesterol molecules) in the CBD was compared with that in the surrounding POPC-cholesterol domain (PCD). In the CBD, ASL and CSL molecules are better ordered than in the surrounding PCD. This difference is small and can be compared to that induced in the surrounding domain by an ~10°C decrease in temperature. Thus, cholesterol molecules are unexpectedly dynamic in the CBD, which should enhance their interaction with the surrounding domain. The polarity of the water/membrane interface of the CBD is significantly greater than that of the surrounding PCD, which significantly enhances penetration of the water-soluble relaxation agent, NiEDDA, into that region. Hydrophobicity measured in the centers of both domains is similar. The oxygen transport parameter (oxygen diffusion-concentration product) measured in the center of the CBD is about ten times smaller than that measured in the center of the surrounding domain. Thus, the CBD can form a significant barrier to oxygen transport. The results presented here point out similarities between the organization and dynamics of cholesterol molecules in the CBD and in the surrounding PCD, as well as significant differences between CBDs and cholesterol crystals.

Indexed as

Biological TransportCholesterolElectron Spin Resonance SpectroscopyHydrophobic and Hydrophilic InteractionsLipid BilayersOxygenPhosphatidylcholinesSpin LabelsTemperature1-palmitoyl-2-oleoylphosphatidylcholineCholesterolLipid BilayersOxygenPhosphatidylcholinesSpin Labels

Identifiers

PMID21855534
PMCPMC3206151

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Registered trials

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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.