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bioRxiv · 10.1101/2025.03.20.644436

High-throughput protein target mapping enables accelerated bioactivity discovery for ToxCast and PFAS compounds

Abstract

Chemical pollution is a global threat to human health, yet the toxicity mechanism of most contaminants remains unknown. Here, we applied an ultrahigh-throughput affinity-selection mass spectrometry (AS-MS) platform to systematically identify protein targets of prioritized chemical contaminants. After benchmarking the platform, we screened 50 human proteins against 481 prioritized chemicals, including 446 ToxCast chemicals and 35 per-and polyfluoroalkyl substances (PFAS). Among 24,050 interactions assessed, we discovered 35 novel interactions involving 14 proteins, with fatty acid-binding proteins (FABPs) emerging as the most ligandable protein family. Given this, we selected FABPs for further validation, which revealed a distinct PFAS binding pattern: legacy PFAS selectively bound to FABP1, whereas replacement compounds, PFECAs, unexpectedly interacted with all FABPs. X-ray crystallography further revealed that the ether group enhances molecular flexibility of alternative PFAS, to accommodate the binding pockets of FABPs. Our findings demonstrate that AS-MS is a robust platform for the discovery of novel protein targets beyond the scope of the ToxCast program and highlight the broader protein-binding spectrum of alternative PFAS as potential regrettable substitutes.

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BibTeXRIS

Yang, D., Wang, X., Liu, J., Nair, P., Sun, J., Gong, Y., Qian, X., Cui, C., Zeng, H., Dong, A., Harding, R. J., Burgess-Brown, N., Beyett, T. S., Song, D., Krause, H., Diamond, M. L., Bolhuis, D. L., Brown, N. G., Arrowsmith, C. H., Edwards, A. M., Halabelian, L., Peng, H.. 2025-03-25. High-throughput protein target mapping enables accelerated bioactivity discovery for ToxCast and PFAS compounds. https://doi.org/10.1101/2025.03.20.644436

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