Evidence map›Paper›PMID 33096080›Full record

ArticleBiophysical journal2020

Structural Model of the Proline-Rich Domain of Huntingtin Exon-1 Fibrils.

Alexander S Falk, José M Bravo-Arredondo, Jobin Varkey, Sayuri Pacheco, Ralf Langen, Ansgar B Siemer

Abstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. What makes functional amyloids work?Critical reviews in biochemistry and molecular biology · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

6 authors.

Alexander S FalkDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California.
José M Bravo-ArredondoDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California.
Jobin VarkeyDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California.
Sayuri PachecoDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California.
Ralf LangenDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California.
Ansgar B SiemerDepartment of Physiology & Neuroscience, Zilkha Neurogenetic Institute, Keck School of Medicine of USC, Los Angeles, California. Electronic address: asiemer@usc.edu.

Funding

Molecular mechanisms of huntingtin misfoldingR01NS084345 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LANGEN, RALF · 2015 to 2019
$2.2M
Orb2 a functional amyloid in long-term memory: Its structure and how it formsR01GM110521 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SIEMER, ANSGAR B · 2015 to 2019
$1.9M
Structure and Kinetics of the Orb2 Functional AmyloidF31GM120858 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FALK, ALEXANDER STOVER · 2017 to 2018
$89k
NIGMS NIH HHS F31 GM120858NIGMS NIH HHS R01 GM110521NINDS NIH HHS R01 NS084345
6 · The paper itself

Abstract

Huntington's disease is a heritable neurodegenerative disease that is caused by a CAG expansion in the first exon of the huntingtin gene. This expansion results in an elongated polyglutamine domain that increases the propensity of huntingtin exon-1 to form cross-β fibrils. Although the polyglutamine domain is important for fibril formation, the dynamic, C-terminal proline-rich domain (PRD) of huntingtin exon-1 makes up a large fraction of the fibril surface. Because potential fibril toxicity has to be mediated by interactions of the fibril surface with its cellular environment, we wanted to model the conformational space adopted by the PRD. We ran 800-ns long molecular dynamics simulations of the PRD using an explicit water model optimized for intrinsically disordered proteins. These simulations accurately predicted our previous solid-state NMR data and newly acquired electron paramagnetic resonance double electron-electron resonance distances, lending confidence in their accuracy. The simulations show that the PRD generally forms an imperfect polyproline (polyP) II helical conformation. The two polyP regions within the PRD stay in a polyP II helix for most of the simulation, whereas occasional kinks in the proline-rich linker region cause an overall bend in the PRD structure. The dihedral angles of the glycine at the end of the second polyP region are very variable, effectively decoupling the highly dynamic 12 C-terminal residues from the rest of the PRD.

Indexed as

Neurodegenerative DiseasesAmyloidExonsHumansHuntingtin ProteinModels, StructuralProlineAmyloidHuntingtin ProteinProline

Identifiers

PMID33096080
PMCPMC7732765

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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.