Covalent Binding of Fluorotelomer Unsaturated Aldehydes (FTUALs) and Carboxylic Acids (FTUCAs) to Proteins
Abstract
Fluorotelomer unsaturated carboxylic acids and aldehydes (FTUCAs and FTUALs) are intermediate compounds that form from the biotransformation of fluorotelomer-based compounds. Previous evidence that FTUCAs and FTUALs bind to biological nucleophiles has indicated that protein binding might give rise to toxicity resulting from protein function disruption. The current study assesses the reactivity of FTUALs and FTUCAs by probing the covalent interactions of FTUALs and FTUCAs with proteins present in rat liver microsomes and bovine blood plasma. The FTUALs exhibited significant levels of protein covalent binding, with binding levels ranging from 20.1 (±2.8)% to 71.3 (±19.5)% in microsomes and 24.0 (±1.5)% to 82.5 (±14.0)% in blood plasma. By contrast, the FTUCAs did not exhibit any apparent covalent binding. Bovine serum albumin (BSA) was extracted and isolated from the plasma after incubation of 8:2 FTUAL (5-100 μM). Electrospray ionization mass spectrometry (ESI-MS) was used to investigate the stoichiometry of 8:2 FTUAL covalently bound to BSA; three measurable FTUAL adducts were formed with BSA. To compare the percent binding results from the FTUAL microsome incubation experiments, 8:2 FTOH was incubated in microsomes to determine the protein binding associated with the biotransformation of 8:2 FTOH. Results from this study showed that the biotransformation of 8:2 FTOH yielded 26.1 (±3.0)% binding, and was statistically similar to the percent binding associated with 8:2 FTUAL e…
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In the case of FTUALs, covalent bond formation occurs via Michael addition.
“In the case of FTUALs, covalent bond formation occurs via Michael addition [58].”
From In-Vitro and In-Silico Assessment of Per- and Polyfluoroalkyl Substances (PFAS) in Aqueous Film-Forming Foam (AFFF) Binding to Human Serum Albumin (2021) · cites this paper as [58]
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- Authors
- Rand, A. A., & Mabury, S. A.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Mabury, Scott A.
- Venue
- Environmental Science & Technology
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-01-09
- Volume
- 47
- Issue
- 3
- Pages
- 130109073401005
- ISSN
- 0013-936X (ISSN-L)
- 1520-5851
- OpenAlex
- W2317473080
- Cited by
- 34
- References
- 55
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 4 · 2022: 2 · 2021: 4 · 2020: 2 · 2019: 5 · 2018: 2 · 2017: 3 · 2016: 3 · 2015: 2 · 2014: 2 · 2013: 3
- FWCI
- 1.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Environmental Science & Technology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Environmental Science › Environmental Chemistry › Per- and polyfluoroalkyl substances research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Interaction Studies and Fluorescence Analysis
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
- Keywords
- covalent protein binding, biotransformation, liver microsomes, blood plasma, bovine serum albumin, adduct stoichiometry, toxicity, perfluorinated compounds
- MeSH terms
- Aldehydes, Animals, Biotransformation, Carboxylic Acids, Cattle, Environment, Fluorides, Humans, Hydrocarbons, Fluorinated, Microsomes, Liver, Plasma, Protein Binding, Serum Albumin, Bovine, Spectrometry, Mass, Electrospray Ionization, Rats
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