Peter John Bond

This study investigates how Ara h 2 and FcϵRI binding affect IgE structural dynamics and allosteric communication, revealing conformational changes and shifts in communication pathways.

This study uses multiscale simulations to reveal how SDS disrupts MS2 bacteriophage capsid, showing pH-dependent effects and molecular mechanisms of surfactant-virus interaction.

This study uses multiscale modeling, lipidomics, and experiments to engineer stable and immunogenic dengue virus-like particles by modifying protein-lipid interactions.

The paper investigates how lipid A modifications in Yersinia species influence pathogenicity by altering TLR4 recognition and inflammation.

This study shows that N153-linked glycans on dengue virus envelope protein help evade antibody-mediated clearance, with implications for immune evasion in related flaviviruses.

This study presents the cryo-EM structure of immature dengue serotype 2 VLPs and uses MD simulations to reveal their maturation mechanism and lipid dependency.

BoPep identifies peptide binders to specific proteins by efficiently navigating sequence space, reducing docking evaluations and discovering novel therapeutic peptides.

This study shows that de-glycosylation of N207 in DENV NS1 reduces viral fitness and enhances clearance by limiting PD-L1/PD-1 mediated T cell apoptosis.

The paper explores the role of allosteric mechanisms in the mutability and druggability of the SARS-CoV-2 Spike protein, identifying potential mutation sites and drug targets.

The paper maps the genome-wide association of capsid proteins with viral RNA in Dengue and Zika viruses, showing non-uniform binding patterns and sequence preferences.

This study maps the structural interactions of dengue and Zika viruses, identifying functional long-range interactions and their role in viral replication and attenuation.