Evidence map›Paper›PMID 35500014›Full record

ArticlePLoS computational biology2022

A topological data analytic approach for discovering biophysical signatures in protein dynamics.

Wai Shing Tang, Gabriel Monteiro da Silva, Henry Kirveslahti, Erin Skeens, Bibo Feng, Timothy Sudijono, Kevin K Yang, Sayan Mukherjee, Brenda Rubenstein, Lorin Crawford

Abstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Generative modeling of biological shapes and images using a probabilisticbioRxiv : the preprint server for biology · 2024
    Article
  7. Article
  8. 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

10 authors.

Wai Shing TangDepartment of Physics, Brown University, Providence, Rhode Island, United States of America.ORCID 0000-0001-7759-7771
Gabriel Monteiro da SilvaDepartment of Molecular and Cell Biology, Brown University, Providence, Rhode Island, United States of America.ORCID 0000-0002-9665-7597
Henry KirveslahtiDepartment of Statistical Science, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-2484-4481
Erin SkeensDepartment of Molecular and Cell Biology, Brown University, Providence, Rhode Island, United States of America.ORCID 0000-0002-0580-1291
Bibo FengDepartment of Chemistry, Brown University, Providence, Rhode Island, United States of America.
Timothy SudijonoDepartment of Statistics, Stanford University, Palo Alto, California, United States of America.ORCID 0000-0002-6075-0378
Kevin K YangMicrosoft Research New England, Cambridge, Massachusetts, United States of America.ORCID 0000-0001-9045-6826
Sayan MukherjeeDepartment of Statistical Science, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-6715-3920
Brenda RubensteinDepartment of Chemistry, Brown University, Providence, Rhode Island, United States of America.ORCID 0000-0003-1643-0358
Lorin CrawfordMicrosoft Research New England, Cambridge, Massachusetts, United States of America.ORCID 0000-0003-0178-8242

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying structural differences among proteins can be a non-trivial task. When contrasting ensembles of protein structures obtained from molecular dynamics simulations, biologically-relevant features can be easily overshadowed by spurious fluctuations. Here, we present SINATRA Pro, a computational pipeline designed to robustly identify topological differences between two sets of protein structures. Algorithmically, SINATRA Pro works by first taking in the 3D atomic coordinates for each protein snapshot and summarizing them according to their underlying topology. Statistically significant topological features are then projected back onto a user-selected representative protein structure, thus facilitating the visual identification of biophysical signatures of different protein ensembles. We assess the ability of SINATRA Pro to detect minute conformational changes in five independent protein systems of varying complexities. In all test cases, SINATRA Pro identifies known structural features that have been validated by previous experimental and computational studies, as well as novel features that are also likely to be biologically-relevant according to the literature. These results highlight SINATRA Pro as a promising method for facilitating the non-trivial task of pattern recognition in trajectories resulting from molecular dynamics simulations, with substantially increased resolution.

Indexed as

Data ScienceMolecular Dynamics SimulationBiophysicsProtein ConformationProteinsProteins

Identifiers

PMID35500014
PMCPMC9098046

What OpenQuestion holds

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LicenceCC BY
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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.