Evidence map›Paper›PMID 26215743›Full record

ArticleBiochimica et biophysica acta2015

Membrane-mediated amyloid formation of PrP 106-126: A kinetic study.

Yen Sun, Wei-Chin Hung, Ming-Tao Lee, Huey W Huang

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. A New Take on Prion Protein Dynamics in Cellular Trafficking.International journal of molecular sciences · 2020
    Review
  3. Article
  4. Article
  5. Article
  6. 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

4 authors at 3 institutions in 2 countries.

Yen SunDepartment of Physics and Astronomy, Rice University, Houston, TX 77005, USA.
Wei-Chin HungDepartment of Physics, R. O. C. Military Academy, Fengshan, Kaohsiung 83055, Taiwan.
Ming-Tao LeeNational Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan; Department of Physics, National Central University, Jhongli 32001, Taiwan.
Huey W HuangDepartment of Physics and Astronomy, Rice University, Houston, TX 77005, USA. Electronic address: hwhuang@rice.edu.
Rice University · USNational Central University · TWR.O.C Military Academy · TW

Funding

Membrane-active Peptides and ProteinsR01GM055203 · NIGMS · RICE UNIVERSITY · PI HUANG, HUEY W. · 1997 to 2017
$5.0M
NIGMS NIH HHS GM55203NIGMS NIH HHS R01 GM055203
6 · The paper itself

Abstract

PrP 106-126 conserves the pathogenic and physicochemical properties of the Scrapie isoform of the prion protein. PrP 106-126 and other amyloidal proteins are capable of inducing ion permeability through cell membranes, and this property may represent the common primary mechanism of pathogenesis in the amyloid-related degenerative diseases. However, for many amyloidal proteins, despite numerous phenomenological observations of their interactions with membranes, it has been difficult to determine the molecular mechanisms by which the proteins cause ion permeability. One approach that has not been undertaken is the kinetic study of protein-membrane interactions. We found that the reaction time constant of the interaction between PrP 106-126 and membranes is suitable for such studies. The kinetic experiment with giant lipid vesicles showed that the membrane area first increased by peptide binding but then decreased. The membrane area decrease was coincidental with appearance of extramembranous aggregates including lipid molecules. Sometimes, the membrane area would increase again followed by another decrease. The kinetic experiment with small vesicles was monitored by circular dichroism for peptide conformation changes. The results are consistent with a molecular simulation following a simple set of well-defined rules. We deduced that at the molecular level the formation of peptide amyloids incorporated lipid molecules as part of the aggregates. Most importantly the amyloid aggregates desorbed from the lipid bilayer, consistent with the macroscopic phenomena observed with giant vesicles. Thus we conclude that the main effect of membrane-mediated amyloid formation is extraction of lipid molecules from the membrane. We discuss the likelihood of this effect on membrane ion permeability.

Indexed as

AmyloidKineticsPeptide FragmentsPhospholipidsPrionsUnilamellar LiposomesAmyloidPeptide FragmentsPhospholipidsprion protein (106-126)PrionsUnilamellar LiposomesAmyloidal peptidesCircular dichroismGiant unilamellar vesiclesLipid extracting effectNeurodegenerative diseasesPrion protein

Identifiers

PMID26215743
PMCPMC4554819
OpenAlexW2111362694

What OpenQuestion holds

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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.