bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.02.14.705892

Molecular Dynamics Analysis of Self and Microbial Peptides Bound to HLA-B27: A Multi-Parameter Framework

Abstract

Molecular mimicry between pathogen-derived and self-peptides shown by MHC molecules is one of the critical mechanisms in the pathophysiology of autoimmune diseases. Numerous studied has been conducted in this field to identify sequence similarity, but evaluating structural and dynamic similarity, systematic computational frameworks remain limited. Therefore, we created an automated multi-parameter molecular dynamics analysis workflow and used it to compare three peptides (KP1, KP2, and KP3) generated from Klebsiella pneumoniae bound to HLA-B class protein with one human self-peptide (Annexin-derived, ANX). We assessed six complementing parameters using one microsecond-scale MD simulation: radius of gyration (Rg), solvent-accessible surface area (SASA), hydrogen bonding dynamics, MM-GBSA binding free energy, root mean square fluctuation (RMSF), and root mean square deviation (RMSD) to understand time-dependent structural and dynamic behaviour of all the peptide-HLA-B complex. Additionally, hydrogen bond occupancy and molecular mechanics generalised Born surface area (MM-GBSA) binding free energy calculations were performed to provide a more comprehensive assessment of complex stability. Our analysis suggests that KP1 exhibits structural features consistent with molecular mimicry, maintaining conformational stability, surface exposure, and interaction patterns comparable to ANX. In contrast, KP2 showed reduced stability, characterised by higher RMSD values and substantial hydrogen bond loss, whereas KP3 displayed intermediate behaviour, with relatively favourable energetics but noticeable conformational variability. Overall, the multi-parameter framework enabled differentiation among the candidate peptides based on combined structural, dynamic, and energetic properties. The workflow can be adapted for the analysis of larger peptide datasets and may provide a systematic approach for investigating potential autoimmune-relevant molecular mimics in microbial proteomes, with required adjustments according to the system.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Singh, S.. 2026-02-17. Molecular Dynamics Analysis of Self and Microbial Peptides Bound to HLA-B27: A Multi-Parameter Framework. https://doi.org/10.64898/2026.02.14.705892

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Common viral infections seed regionally distinct resident memory T cells in the human CNS

T cells persist in the central nervous system (CNS) and can drive both protection and neurological disease. How these cells are organized in humans and what they recognize is largely unknown. Here, we profiled CD8 T cells across anatomically distinct CNS regions, obtained through on-site autopsies and temporal lobe resection surgeries, using single-cell RNA sequencing, paired T cell receptor sequencing, and DNA-barcoded tetramers. Resident memory T cells (TRM) specific for Epstein-Barr virus, cytomegalovirus, influenza A, and SARS-CoV-2 were identified across CNS compartments. Anatomical location was the strongest correlate of TRM cell state, with leptomeningeal cells adopting a cytokine-poised TRM program, whereas brain TRM cells were transcriptionally restrained. Cells of the same clonotype spanned tissues yet adopted local transcriptional states. Viral specificity added another layer of TRM heterogeneity with GZMK/GZMA-expressing EBV-specific populations and interferon-stimulated gene signatures in SARS-CoV-2 and Influenza A-specific cells. The human CNS thus harbors regionally distinct CD8+ TRM shaped by common viral exposures.

immunology↗

A regulatory T cell signature provides a shared molecular basis for the therapeutic window of opportunity in rheumatic disease

Rheumatic diseases, including rheumatoid arthritis (RA), spondyloarthritis (SpA) and osteoarthritis (OA), show distinct phenotypes yet respond to overlapping therapies, implicating shared immune mechanisms. In the Transimmunom cohort, we profiled peripheral blood from 240 individuals (47 healthy, 44 OA, 91 RA, 58 SpA) across deep immunophenotyping, immunoproteomics and Treg-Teff transcriptomics. Single-layer analyses revealed broader Treg than Teff remodeling, along with a shared pattern of reduced activated Tregs and expanded Helios+ Tregs across all diseases, alongside a decrease in functional Treg subpopulations, including CTLA4+ and CD45RA- Tregs. In RA specifically, LAG3+ Tregs were also expanded. Combining omics layers outperformed single-layer approaches for disease classification. Among individual layers, Treg transcriptomes were most discriminative, and integration uncovered disease-specific programs. Unsupervised clustering identified a cross-disease cluster independent of activity, treatment and age, mapping to early disease (<= years) and dominated by a Treg dysfunction-associated program. These results provide a biological rationale for the therapeutic "window of opportunity" concept and duration-stratified Treg-directed trials.

immunology↗

Inhibitory Fc Receptor sets a time limit on macrophage response to IgG

Antibodies engage both activating Fc Receptors and the inhibitory receptor Fc{gamma}RIIB. Why macrophages need a dedicated inhibitory receptor rather than simply tuning activating receptor signaling is unclear. Using DNA-based chimeric receptors and in silico modeling, we independently controlled activating and inhibitory Fc Receptors. We found that Fc{gamma}RIIB imposed a time limit on macrophage phagocytosis and ERK signaling. The time limit is due to activating Fc Receptors converting PI(4,5)P2 to PI(3,4,5)P3, which is subsequently converted to PI(3,4)P2 by Fc{gamma}RIIB. This leads to a pulse of active signaling, which is sufficient for phagocytosis of small bacteria-sized targets but not phagocytosis of large targets and TNF secretion. Unlike engaging Fc{gamma}RIIB, reducing activating Fc Receptor signaling decreased initiation of phagocytosis, the speed of PI(3,4,5)P3 generation, and the amplitude of ERK signaling. Our results demonstrate that Fc{gamma}RIIB controls the duration of IgG signaling, while the activating Fc Receptors control sensitivity.

immunology↗