Evidence map›Paper›PMID 33291927›Full record

ArticleThe Journal of chemical physics2020

Data-guided Multi-Map variables for ensemble refinement of molecular movies.

John W Vant, Daipayan Sarkar, Ellen Streitwieser, Giacomo Fiorin, Robert Skeel, Josh V Vermaas, Abhishek Singharoy

Abstract read
In one paragraph

Article in The Journal of chemical physics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Expanded Functionality and Portability for the Colvars Library.The journal of physical chemistry. B · 2024
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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

7 authors.

John W VantSchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, USA.ORCID 0000000306274603
Daipayan SarkarSchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, USA.ORCID 0000000241672108
Ellen StreitwieserSchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, USA.ORCID 0000000172381656
Giacomo FiorinTheoretical Molecular Biophysics Laboratory, National Heart, Lung and Blood Institute, National Institutes of Health, 10 Center Drive, Bethesda, Maryland 20814, USA.ORCID 0000000287938645
Robert SkeelSchool of Mathematical and Statistical Sciences, Arizona State University, Tempe, Arizona 85281, USA.ORCID 0000000248078988
Josh V VermaasComputing and Computational Sciences Directorate, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, USA.ORCID 0000000331396469
Abhishek SingharoySchool of Molecular Sciences, Arizona State University, Tempe, Arizona 85281, USA.ORCID 0000000290002397

Funding

Femtosecond nano-crystallography of membrane proteinsR01GM095583 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI FROMME, PETRA · 2010 to 2023
$4.3M
NIGMS NIH HHS R01 GM095583
6 · The paper itself

Abstract

Driving molecular dynamics simulations with data-guided collective variables offer a promising strategy to recover thermodynamic information from structure-centric experiments. Here, the three-dimensional electron density of a protein, as it would be determined by cryo-EM or x-ray crystallography, is used to achieve simultaneously free-energy costs of conformational transitions and refined atomic structures. Unlike previous density-driven molecular dynamics methodologies that determine only the best map-model fits, our work employs the recently developed Multi-Map methodology to monitor concerted movements within equilibrium, non-equilibrium, and enhanced sampling simulations. Construction of all-atom ensembles along the chosen values of the Multi-Map variable enables simultaneous estimation of average properties, as well as real-space refinement of the structures contributing to such averages. Using three proteins of increasing size, we demonstrate that biased simulation along the reaction coordinates derived from electron densities can capture conformational transitions between known intermediates. The simulated pathways appear reversible with minimal hysteresis and require only low-resolution density information to guide the transition. The induced transitions also produce estimates for free energy differences that can be directly compared to experimental observables and population distributions. The refined model quality is superior compared to those found in the Protein Data Bank. We find that the best quantitative agreement with experimental free-energy differences is obtained using medium resolution density information coupled to comparatively large structural transitions. Practical considerations for probing the transitions between multiple intermediate density states are also discussed.

Indexed as

Models, ChemicalAdenylate KinaseAldehyde OxidoreductasesCryoelectron MicroscopyLipoproteinsMolecular Dynamics SimulationMultienzyme ComplexesProtein ConformationProteinsThermodynamicsAdenylate KinaseAldehyde Oxidoreductasescarbon monoxide dehydrogenaseLipoproteinsMultienzyme ComplexesProteins

Identifiers

PMID33291927
PMCPMC7714525

What OpenQuestion holds

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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.