Salvato in:
Dettagli Bibliografici
Autori principali: Chang, Tien-Lin, Sun, Hsiao-Yu, Sung, Ping-Jyun, Sun, Hsi-Wen
Natura: Artículo científico
Lingua:en
Pubblicazione: International journal of molecular sciences 2026
Soggetti:
Accesso online:https://pubmed.ncbi.nlm.nih.gov/41828473/
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1868266074568392704
author Chang, Tien-Lin
Sun, Hsiao-Yu
Sung, Ping-Jyun
Sun, Hsi-Wen
author_facet Chang, Tien-Lin
Sun, Hsiao-Yu
Sung, Ping-Jyun
Sun, Hsi-Wen
Chang, Tien-Lin
Sun, Hsiao-Yu
Sung, Ping-Jyun
Sun, Hsi-Wen
collection PubMed - marine biology
contents Computational Analysis of Excavatolide B-Human STING Interactions Implicates a Cys148-Adjacent Corridor with Within-Cavity Sub-Pose Diversity. Chang, Tien-Lin Sun, Hsiao-Yu Sung, Ping-Jyun Sun, Hsi-Wen Humans Molecular Dynamics Simulation Molecular Docking Simulation Membrane Proteins Diterpenes Binding Sites Protein Binding Cysteine STING Protein Chronic, dysregulated inflammation contributes to colitis-associated colorectal cancer (CRC), and the cGAS-STING pathway represents a central but therapeutically challenging node because both insufficient and excessive STING activity can be pathogenic. Here, we integrate AlphaFold3 (AF3) receptor modeling, diffusion-based docking, and explicit-solvent molecular dynamics (MD) simulations to characterize how the marine briarane diterpenoid excavatolide B (ExcB) engages the human STING (hSTING) cyclic dinucleotide (CDN)-binding cleft. The structural integrity of the AF3 hSTING model was validated through both intrinsic confidence scores (pLDDT, PAE) and comparative benchmarking against experimental CTD structures (PDB: 4EF5, 6A05). Notably, the local geometries of key pocket-defining residues-including His157, Tyr167, and Thr263-remained consistent with established crystallographic data. Across three independent 100 ns MD replicas, ExcB exhibits a consistent spatial progression from an entrance-proximal pose at the solvent-accessible rim of the cleft (Site-2) to a more embedded, non-canonical corridor on the Cys148-adjacent side (Site-2'). Distance and contact analyses support a predominantly non-covalent within-cleft mechanism and do not indicate a persistent approach to the literature-reported covalent regime near Cys91. Residue-level profiling over the stabilized sampling window defines a reproducible corridor "contact signature" and reveals within-cavity sub-pose diversity rather than a single rigid bound pose. Mechanistically, competitive docking of the native agonist cGAMP to ExcB-conditioned receptor snapshots yields consistently less favorable docking outcomes in ExcB-conditioned conformations than docking to the native/open receptor; retaining ExcB coordinates does not further penalize cGAMP, supporting a receptor-reshaping (conformational conditioning) component rather than persistent static steric clash. Our findings characterize ExcB as a non-covalent modulator targeting a cryptic pocket within the STING CDN-binding cleft, establishing a structural basis for targeted mutagenesis and structure-activity relationship (SAR) studies.
format Artículo científico
id pubmed_41828473
institution PubMed
language en
publishDate 2026
publisher International journal of molecular sciences
record_format pubmed
spellingShingle Computational Analysis of Excavatolide B-Human STING Interactions Implicates a Cys148-Adjacent Corridor with Within-Cavity Sub-Pose Diversity.
Chang, Tien-Lin
Sun, Hsiao-Yu
Sung, Ping-Jyun
Sun, Hsi-Wen
Humans
Molecular Dynamics Simulation
Molecular Docking Simulation
Membrane Proteins
Diterpenes
Binding Sites
Protein Binding
Cysteine
STING Protein
Computational Analysis of Excavatolide B-Human STING Interactions Implicates a Cys148-Adjacent Corridor with Within-Cavity Sub-Pose Diversity. Chang, Tien-Lin Sun, Hsiao-Yu Sung, Ping-Jyun Sun, Hsi-Wen Humans Molecular Dynamics Simulation Molecular Docking Simulation Membrane Proteins Diterpenes Binding Sites Protein Binding Cysteine STING Protein Chronic, dysregulated inflammation contributes to colitis-associated colorectal cancer (CRC), and the cGAS-STING pathway represents a central but therapeutically challenging node because both insufficient and excessive STING activity can be pathogenic. Here, we integrate AlphaFold3 (AF3) receptor modeling, diffusion-based docking, and explicit-solvent molecular dynamics (MD) simulations to characterize how the marine briarane diterpenoid excavatolide B (ExcB) engages the human STING (hSTING) cyclic dinucleotide (CDN)-binding cleft. The structural integrity of the AF3 hSTING model was validated through both intrinsic confidence scores (pLDDT, PAE) and comparative benchmarking against experimental CTD structures (PDB: 4EF5, 6A05). Notably, the local geometries of key pocket-defining residues-including His157, Tyr167, and Thr263-remained consistent with established crystallographic data. Across three independent 100 ns MD replicas, ExcB exhibits a consistent spatial progression from an entrance-proximal pose at the solvent-accessible rim of the cleft (Site-2) to a more embedded, non-canonical corridor on the Cys148-adjacent side (Site-2'). Distance and contact analyses support a predominantly non-covalent within-cleft mechanism and do not indicate a persistent approach to the literature-reported covalent regime near Cys91. Residue-level profiling over the stabilized sampling window defines a reproducible corridor "contact signature" and reveals within-cavity sub-pose diversity rather than a single rigid bound pose. Mechanistically, competitive docking of the native agonist cGAMP to ExcB-conditioned receptor snapshots yields consistently less favorable docking outcomes in ExcB-conditioned conformations than docking to the native/open receptor; retaining ExcB coordinates does not further penalize cGAMP, supporting a receptor-reshaping (conformational conditioning) component rather than persistent static steric clash. Our findings characterize ExcB as a non-covalent modulator targeting a cryptic pocket within the STING CDN-binding cleft, establishing a structural basis for targeted mutagenesis and structure-activity relationship (SAR) studies.
title Computational Analysis of Excavatolide B-Human STING Interactions Implicates a Cys148-Adjacent Corridor with Within-Cavity Sub-Pose Diversity.
topic Humans
Molecular Dynamics Simulation
Molecular Docking Simulation
Membrane Proteins
Diterpenes
Binding Sites
Protein Binding
Cysteine
STING Protein
url https://pubmed.ncbi.nlm.nih.gov/41828473/