Evidence map›Paper›PMID 33168711›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Michler's hydrol blue elucidates structural differences in prion strains.

Yiling Xiao, Sandra Rocha, Catherine C Kitts, Anna Reymer, Tamás Beke-Somfai, Kendra K Frederick, Bengt Nordén

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

7 authors at 4 institutions in 3 countries.

Yiling XiaoDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390-8816.ORCID 0000-0002-4548-4833
Sandra RochaDepartment of Biology and Biological Engineering, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.ORCID 0000-0002-4530-3537
Catherine C KittsDepartment of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.
Anna ReymerDepartment of Chemistry and Molecular Biology, University of Gothenburg, SE-405 30 Gothenburg, Sweden.
Tamás Beke-SomfaiInstitute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Hungarian Academy of Sciences, H-1117 Budapest, Hungary.ORCID 0000-0002-4788-3758
Kendra K FrederickDepartment of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390-8816; kendra.frederick@utsouthwestern.edu norden@chalmers.se.ORCID 0000-0002-1656-5167
Bengt NordénDepartment of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden; kendra.frederick@utsouthwestern.edu norden@chalmers.se.
Chalmers University of Technology · SEThe University of Texas Southwestern Medical Center · USInstitute of Materials and Environmental Chemistry · HUUniversity of Gothenburg · SE

Funding

High sensitivity NMR for structure determination of neurodegenerative disease associated protein aggregates in native contextsDP2NS111236 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI FREDERICK, KENDRA KING · 2018 to 2018
$2.4M
NINDS NIH HHS DP2 NS111236
6 · The paper itself

Abstract

Yeast prions provide self-templating protein-based mechanisms of inheritance whose conformational changes lead to the acquisition of diverse new phenotypes. The best studied of these is the prion domain (NM) of Sup35, which forms an amyloid that can adopt several distinct conformations (strains) that confer distinct phenotypes when introduced into cells that do not carry the prion. Classic dyes, such as thioflavin T and Congo red, exhibit large increases in fluorescence when bound to amyloids, but these dyes are not sensitive to local structural differences that distinguish amyloid strains. Here we describe the use of Michler's hydrol blue (MHB) to investigate fibrils formed by the weak and strong prion fibrils of Sup35NM and find that MHB differentiates between these two polymorphs. Quantum mechanical time-dependent density functional theory (TDDFT) calculations indicate that the fluorescence properties of amyloid-bound MHB can be correlated to the change of binding site polarity and that a tyrosine to phenylalanine substitution at a binding site could be detected. Through the use of site-specific mutants, we demonstrate that MHB is a site-specific environmentally sensitive probe that can provide structural details about amyloid fibrils and their polymorphs.

Indexed as

AmyloidAniline CompoundsBenzhydryl CompoundsBinding SitesCongo RedFluorescenceFungal ProteinsPeptide Termination FactorsPrionsProtein DomainsYeastsAmyloidAniline CompoundsBenzhydryl CompoundsCongo RedFungal ProteinsMichler's hydrol bluePeptide Termination FactorsPrionsamyloid dyeamyloid fibrilfluorescence spectroscopyprionSup35NM

Identifiers

PMID33168711
PMCPMC7703575
OpenAlexW3101928296

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.