In vitro biolayer interferometry analysis of acetylcholinesterase as a potential target of aryl-organophosphorus flame-retardants

Highlights: • Inhibition of AChE by OPFRs was evaluated in zebrafish larvae. • Aryl-OPFRs inhibited AChE activity, but chlorinated- and alkyl-OPFRs did not. • Biolayer interferometry showed that aryl-OPFRs bind AChE. • Molecular docking showed that aryl-OPFRs interact more strongly than other OPFRs. • Aryl-OPFRs are potent neurotoxicants that posing a risk to aquatic organisms. Organophosphorus flame retardants (OPFRs) have been implicated as neurotoxicants, but their potential neurotoxicity and mechanisms remain poorly understood. Herein, we investigated the neurotoxicity of selected OPFRs using zebrafish as a model organism. Environmentally relevant concentrations (3–1500 nM) of three classes of OPFRs (aryl-OPFRs, chlorinated-OPFRs, and alkyl-OPFRs) were tested in zebrafish larvae (2–144 h post-fertilisation) alongside the neurotoxic chemical chlorpyrifos (CPF) that inhibits acetylcholinesterase (AChE). Exposure to aryl-OPFRs and CPF inhibited AChE activities, while chlorinated- and alkyl-OPFRs did not inhibit these enzymes. Biolayer interferometry (BLI) was used to probe interactions between OPFRs and AChE. The association and dissociation response curves showed that, like CPF, all three selected aryl-OPFRs, triphenyl phosphate (TPHP), tricresyl phosphate (TCP) and cresyl diphenyl phosphate (CDP), bound directly to AChE. The affinity constant (K_D) for TPHP, TCP, CDP and CPF was 2.18 × 10⁻⁴, 5.47 × 10⁻⁵, 1.05 × 10⁻⁴ and 1.70 × 10⁻⁵ M, respectively. In addition, molecular docking revealed that TPHP, TCP, CDP and CPF bound to AChE with glide scores of − 7.8, − 8.3, − 8.1 and − 7.3, respectively. Furthermore, the calculated binding affinity between OPFRs and AChE correlated well with the K_D values measured by BLI. The present study revealed that aryl-OPFRs can act as potent AChE inhibitors, and may therefore present a significant ecological risk to aquatic organisms.