Evidence map›Paper›PMID 25849085›Full record

ArticleACS applied materials & interfaces2015

Spectroscopic Characterization of Structural Changes in Membrane Scaffold Proteins Entrapped within Mesoporous Silica Gel Monoliths.

Wade F Zeno, Silvia Hilt, Subhash H Risbud, John C Voss, Marjorie L Longo

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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4 · The record

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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.

Wade F Zeno†Department of Chemical Engineering and Materials Science and ‡Department of Biochemistry and Molecular Medicine, University of California at Davis, Davis, California 95616, United States.
Silvia Hilt†Department of Chemical Engineering and Materials Science and ‡Department of Biochemistry and Molecular Medicine, University of California at Davis, Davis, California 95616, United States.
Subhash H Risbud†Department of Chemical Engineering and Materials Science and ‡Department of Biochemistry and Molecular Medicine, University of California at Davis, Davis, California 95616, United States.
John C Voss†Department of Chemical Engineering and Materials Science and ‡Department of Biochemistry and Molecular Medicine, University of California at Davis, Davis, California 95616, United States.
Marjorie L Longo†Department of Chemical Engineering and Materials Science and ‡Department of Biochemistry and Molecular Medicine, University of California at Davis, Davis, California 95616, United States.

Funding

Training Program in Biomolecular TechnologyT32GM008799 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI LEACH, J. KENT · 2002 to 2016
$2.4M
NIGMS NIH HHS T32 GM008799NIGMS NIH HHS T32-GM008799
6 · The paper itself

Abstract

The changes in the orientation and conformation of three different membrane scaffold proteins (MSPs) upon entrapment in sol-gel-derived mesoporous silica monoliths were investigated. MSPs were examined in either a lipid-free or a lipid-bound conformation, where the proteins were associated with lipids to form nanolipoprotein particles (NLPs). NLPs are water-soluble, disk-shaped patches of a lipid bilayer that have amphiphilic MSPs shielding the hydrophobic lipid tails. The NLPs in this work had an average thickness of 5 nm and diameters of 9.2, 9.7, and 14.8 nm. We have previously demonstrated that NLPs are more suitable lipid-based structures for silica gel entrapment than liposomes because of their size compatibility with the mesoporous network (2-50 nm) and minimally altered structure after encapsulation. Here we further elaborate on that work by using a variety of spectroscopic techniques to elucidate whether or not different MSPs maintain their protein-lipid interactions after encapsulation. Fluorescence spectroscopy and quenching of the tryptophan residues with acrylamide, 5-DOXYL-stearic acid, and 16-DOXYL-stearic acid were used to determine the MSP orientation. We also utilized fluorescence anisotropy of tryptophans to measure the relative size of the NLPs and MSP aggregates after entrapment. Finally, circular dichroism spectroscopy was used to examine the secondary structure of the MSPs. Our results showed that, after entrapment, all of the lipid-bound MSPs maintained orientations that were minimally changed and indicative of association with lipids in NLPs. The tryptophan residues appeared to remain buried within the hydrophobic core of the lipid tails in the NLPs and appropriately spaced from the bilayer center. Also, after entrapment, lipid-bound MSPs maintained a high degree of α-helical content, a secondary structure associated with protein-lipid interactions. These findings demonstrate that NLPs are capable of serving as viable hosts for functional integral membrane proteins in the synthesis of sol-gel-derived bioinorganic hybrid nanomaterials.

Indexed as

AcrylamideAmino Acid SequenceAnisotropyCircular DichroismLipoproteinsMembrane ProteinsMolecular Sequence DataNanoparticlesPorositySilica GelSolutionsSpectrometry, FluorescenceTryptophanAcrylamideLipoproteinsMembrane ProteinsSilica GelSolutionsTryptophanbiohybrid materialmembrane scaffold proteinmesoporous silicananolipoprotein particleprotein−lipid interactionstryptophan fluorescence

Identifiers

PMID25849085
PMCPMC5522711

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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.