Evidence map›Paper›PMID 40677241›Full record

ArticleComputational and structural biotechnology journal2025

Predicting receptor-ligand pairing preferences in plant-microbe interfaces via molecular dynamics and machine learning.

Erica T Prates, Omar Demerdash, Manesh Shah, Tomás A Rush, Udaya C Kalluri, Daniel A Jacobson

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. AlphaFold in protein structure and function prediction.Computational and structural biotechnology journal · 2025
    Article
  4. Review
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.

Erica T PratesBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA.
Omar DemerdashBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA.
Manesh ShahGenome Science and Technology, The University of Tennessee-Knoxville, Knoxville, TN 37996, USA.
Tomás A RushBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA.
Udaya C KalluriBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA.
Daniel A JacobsonBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbiome assembly, structure, and dynamics significantly influence plant health. Secreted microbial signaling molecules initiate and mediate symbiosis by binding to structurally compatible plant receptors. For example, lipo-chitooligosaccharides (LCOs), produced by nitrogen-fixing rhizobial bacteria and various fungi, are recognized by plant lysin motif receptor-like kinases (LysM-RLKs), which activate the common symbiotic pathway. Accurately predicting these molecular interactions could reveal complementary signatures underlying the initial stages of endosymbiosis. Despite the breakthrough in protein-ligand structure prediction with deep learning-based tools, such as AlphaFold3, the large size and highly flexible nature of signaling compounds like LCOs present major challenges for detailed structural characterization and binding-affinity prediction. Typical structure-/physics-based methods of ligand virtual screening are designed for small, drug-like molecules, often rely on high-resolution, experimentally determined structures of the protein receptors, and rarely achieve sufficient sampling to obtain converged thermodynamic quantities with large ligands. In this study, we developed a hybrid molecular dynamics/machine learning (MD/ML) approach capable of predicting binding affinity rankings with high accuracy in systems involving large, flexible ligands, despite limited experimental structural information. Using coarse initial structural models, the predictions using the MD/ML workflow achieved strong alignment with experimental trends, particularly in the top-affinity tier for four legume LysM-RLKs (LYR3) binding to LCOs and a chitooligosaccharide. Furthermore, the MD-based conformation selection protocol provided critical structural insights into substrate specificity and binding mechanisms. This study demonstrates a powerful method to screen for challenging cognate ligand-receptors and advance our understanding of the molecular basis of microbial colonization in plants.

Indexed as

Lipo-chitooligosaccharidesLysMMachine learningPlant-microbe interactionsProtein-ligand binding affinity predictionSignaling molecules

Identifiers

PMID40677241
PMCPMC12270019

What OpenQuestion holds

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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.