[In silico analysis of molecular mimicry between human aquaporin 3, Aspergillus fumigatus aquaporin and aquaporins from allergic sources].

Objective: Conduct an in-silico assessment of potential molecular mimicry between human aquaporins, , and diverse allergenic sources.

Methods: Amino acid sequences of human AQP3 and aquaporin were compared through multiple alignments with 25 aquaporins from diverse allergenic sources. Phylogenetic analysis and homology-based modeling were executed, and the ElliPro server predicted conserved antigenic regions on 3D structures.

Results: Global identity among studied aquaporins was 32.6%, with a specific conserved local region at 71.4%. Five monophyletic clades (A-E) were formed, and Group B displayed the highest identity (95%), including 6 mammalian aquaporins, notably AQP3. aquaporin exhibited the highest identity with Malassezia sympodialis (35%). Three linear and three discontinuous epitopes were identified in both human and aquaporins. The Root Mean Square Deviation (RMSD) from overlapping aquaporin structures was 1.006.

Conclusion: Identification of potential linear and conformational epitopes on human AQP3 suggests likely molecular mimicry with aquaporins. High identity in a specific antigenic region indicates potential autoreactivity and a probable antigenic site involved in cross-reactivity. Validation through in vitro and in vivo studies is essential for further understanding and confirmation.