Evidence map›Paper›PMID 33581430›Full record

ArticleBiophysical chemistry2021

Effects of pH on an IDP conformational ensemble explored by molecular dynamics simulation.

Richard J Lindsay, Rachael A Mansbach, S Gnanakaran, Tongye Shen

Open access · greenAbstract read
In one paragraph

Article in Biophysical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 37 citations in OpenAlex.

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  12. A modular approach to map out the conformational landscapes of unbound intrinsically disordered proteins.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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 2 institutions in 2 countries.

Richard J LindsayUT- ORNL Graduate School of Genome Science and Technology, Knoxville, TN, 37996, USA. Electronic address: rlindsa2@vols.utk.edu.
Rachael A MansbachTheoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, 87544, USA; Department of Physics, Concordia University, Montreal, Quebec, Canada. Electronic address: re.mansbach@concordia.ca.
S GnanakaranTheoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM, 87544, USA. Electronic address: gnana@lanl.gov.
Tongye ShenDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, TN, 37996, USA. Electronic address: tshen@utk.edu.
Los Alamos National Laboratory · USUniversity of Tennessee at Knoxville · US

Funding

Role of Allostery in CAR TransactivationR15GM123469 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI FERNANDEZ, ELIAS J, MCCORD, RACHEL PATTON · 2017 to 2017
$453k
NIGMS NIH HHS R15 GM123469
6 · The paper itself

Abstract

The conformational ensemble of intrinsically disordered proteins, such as α-synuclein, are responsible for their function and malfunction. Misfolding of α-synuclein can lead to neurodegenerative diseases, and the ability to study their conformations and those of other intrinsically disordered proteins under varying physiological conditions can be crucial to understanding and preventing pathologies. In contrast to well-folded peptides, a consensus feature of IDPs is their low hydropathy and high charge, which makes their conformations sensitive to pH perturbation. We examine a prominent member of this subset of IDPs, α-synuclein, using a divide-and-conquer scheme that provides enhanced sampling of IDP structural ensembles. We constructed conformational ensembles of α-synuclein under neutral (pH ~ 7) and low (pH ~ 3) pH conditions and compared our results with available information obtained from smFRET, SAXS, and NMR studies. Specifically, α-synuclein has been found to in a more compact state at low pH conditions and the structural changes observed are consistent with those from experiments. We also characterize the conformational and dynamic differences between these ensembles and discussed the implication on promoting pathogenic fibril formation. We find that under low pH conditions, neutralization of negatively charged residues leads to compaction of the C-terminal portion of α-synuclein while internal reorganization allows α-synuclein to maintain its overall end-to-end distance. We also observe different levels of intra-protein interaction between three regions of α-synuclein at varying pH and a shift towards more hydrophilic interactions with decreasing pH.

Indexed as

Molecular Dynamics SimulationHydrogen-Ion ConcentrationIntrinsically Disordered ProteinsProtein ConformationIntrinsically Disordered ProteinsAlpha-synucleinFRETIntrinsically disordered proteinMolecular dynamics

Identifiers

PMID33581430
PMCPMC8024028
OpenAlexW3125782427

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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.