Evidence map›Paper›PMID 31756784›Full record

ArticleJournal of mass spectrometry : JMS2020

Investigating the interactions of the first 17 amino acid residues of Huntingtin with lipid vesicles using mass spectrometry and molecular dynamics.

Ahmad Kiani Karanji, Maryssa Beasley, Daud Sharif, Ali Ranjbaran, Justin Legleiter, Stephen J Valentine

Open access · greenAbstract read
In one paragraph

Article in Journal of mass spectrometry : JMS, 2020. 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
0.9field-weighted citation impact, top 25% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Lipid headgroups alter huntingtin aggregation on membranes.Biochimica et biophysica acta. Biomembranes · 2021
    Article
  6. Review
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

6 authors at 1 institution in 1 country.

Ahmad Kiani KaranjiC. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26506.
Maryssa BeasleyC. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26506.
Daud SharifC. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26506.
Ali RanjbaranDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, WV, 26506.
Justin LegleiterC. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26506.
Stephen J ValentineC. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26506.ORCID https://orcid.org/0000-0003-4360-2928
West Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI JUDITH FEINBERG · 2012 to 2026
$81.0M
Developing IMS-SID/MAD-MS Instrumentation for Characterizing Intrinsically Disordered Protein StructureR01GM114494 · NIGMS · WEST VIRGINIA UNIVERSITY · PI VALENTINE, STEPHEN · 2015 to 2019
$1.4M
NIGMS NIH HHS R01 GM114494NIGMS NIH HHS U54 GM104942NIH HHS R01GM114494
6 · The paper itself

Abstract

The first 17 amino acid residues of Huntingtin protein (Nt17 of htt) are thought to play an important role in the protein's function; Nt17 is one of two membrane binding domains in htt. In this study the binding ability of Nt17 peptide with vesicles comprised of two subclasses of phospholipids is studied using electrospray ionization - mass spectrometry (ESI-MS) and molecular dynamics (MD) simulations. Overall, the peptide is shown to have a greater propensity to interact with vesicles of phosphatidylcholine (PC) rather than phosphatidylethanolamine (PE) lipids. Mass spectra show an increase in lipid-bound peptide adducts where the ordering of the number of such specie is 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) > 1-palmitoyl-2-oleoyl-glycero-3-phosphocholine (POPC) > 1-palmitoyl-2-oleoyl-sn-glycero-3 phosphoethanolamine (POPE). MD simulations suggest that the compactness of the bilayer plays a role in governing peptide interactions. The peptide shows greater disruption of the DOPC bilayer order at the surface and interacts with the hydrophobic tails of lipid molecules via hydrophobic residues. Conversely, the POPE vesicle remains ordered and lipids display transient interactions with the peptide through the formation of hydrogen bonds with hydrophilic residues. The POPC system displays intermediate behavior with regard to the degree of peptide-membrane interaction. Finally, the simulations suggest a helix stabilizing effect resulting from the interactions between hydrophobic residues and the lipid tails of the DOPC bilayer.

Indexed as

Molecular Dynamics SimulationAmino AcidsHuntingtin ProteinHydrogen BondingHydrophobic and Hydrophilic InteractionsPeptidesPhospholipidsProtein BindingSpectrometry, Mass, Electrospray IonizationStructure-Activity RelationshipAmino AcidsHuntingtin ProteinPeptidesPhospholipidsHuntingtinmolecular dynamics simulationsnative MSpeptide interactionsProtein aggregation

Identifiers

PMID31756784
PMCPMC7342490
OpenAlexW2990859539

What OpenQuestion holds

Textmetadata
LicenceTDM
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.