Evidence map›Paper›PMID 38297834›Full record

ArticleBiophysical journal2024

Generative β-hairpin design using a residue-based physicochemical property landscape.

Vardhan Satalkar, Gemechis D Degaga, Wei Li, Yui Tik Pang, Andrew C McShan, James C Gumbart, Julie C Mitchell, Matthew P Torres

Abstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Vardhan SatalkarSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia.
Gemechis D DegagaBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee.
Wei LiSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia.
Yui Tik PangSchool of Physics, Georgia Institute of Technology, Atlanta, Georgia.
Andrew C McShanSchool of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia.
James C GumbartSchool of Physics, Georgia Institute of Technology, Atlanta, Georgia; School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia.
Julie C MitchellBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee. Electronic address: mitchelljc@ornl.gov.
Matthew P TorresSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia; School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia. Electronic address: mtorres35@gatech.edu.

Funding

Elucidating the mechanisms of protein secretion across the outer membrane by bacterial autotransportersR01GM148586 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI James C. Gumbart · 2023 to 2026
$1.8M
NIGMS NIH HHS R01 GM148586
6 · The paper itself

Abstract

De novo peptide design is a new frontier that has broad application potential in the biological and biomedical fields. Most existing models for de novo peptide design are largely based on sequence homology that can be restricted based on evolutionarily derived protein sequences and lack the physicochemical context essential in protein folding. Generative machine learning for de novo peptide design is a promising way to synthesize theoretical data that are based on, but unique from, the observable universe. In this study, we created and tested a custom peptide generative adversarial network intended to design peptide sequences that can fold into the β-hairpin secondary structure. This deep neural network model is designed to establish a preliminary foundation of the generative approach based on physicochemical and conformational properties of 20 canonical amino acids, for example, hydrophobicity and residue volume, using extant structure-specific sequence data from the PDB. The beta generative adversarial network model robustly distinguishes secondary structures of β hairpin from α helix and intrinsically disordered peptides with an accuracy of up to 96% and generates artificial β-hairpin peptide sequences with minimum sequence identities around 31% and 50% when compared against the current NCBI PDB and nonredundant databases, respectively. These results highlight the potential of generative models specifically anchored by physicochemical and conformational property features of amino acids to expand the sequence-to-structure landscape of proteins beyond evolutionary limits.

Indexed as

PeptidesAmino Acid SequenceHydrophobic and Hydrophilic InteractionsModels, MolecularNeural Networks, ComputerProtein Structure, SecondaryPeptides

Identifiers

PMID38297834
PMCPMC11393682

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.