|
|
Potential human accumulation difference of polyhalogenated carbazoles pollutants |
MA Jun-chao1,2, QIN Chao2, WANG Ze-ming2, LI Ze-kai2, GAO Yan-zheng2 |
1. School of Biological and Environmental Engineering, Chaohu Regional Collaborative Technology Service Center for Rural Revitalization, Chaohu University, Hefei 238000, China; 2. Institute of Organic Contaminant Control and Soil Remediation, Nanjing Agricultural University, Nanjing 210095, China |
|
|
Abstract To evaluate the potential human accumulation difference and mechanism of polyhalogenated carbazoles (PHCZs), this study chose human serum albumin (HSA) as a model protein and used spectroscopy and quantum chemical calculations to analyze the interaction effects between HSA and four typical PHCZs, i.e., 3-bromocarbazole (3BCZ), 2,7-dibromocarbazole (27BCZ), 3,6-dibromocarbazole (36BCZ), and 3,6-dichlorocarbazole (36CCZ). All four PHCZs could bind to site 2 of HSA, with the order of intermolecular binding strength as follows: 36BCZ (3.89×105L/mol) > 36CCZ (3.41×105L/mol) > 3BCZ (1.43×105L/mol) > 27BCZ (2.95×104L/mol). Due to the better stability of intermolecular binding and minimal damage to the HSA structure, different PHCZs may have a stronger potential for bioaccumulation in the human body. Quantum chemical calculations indicated that the size and distribution of the negative molecular surface electrostatic potential area of PHCZs played a decisive role in intermolecular binding. This study revealed the potential human accumulation difference and mechanism of common PHCZs, which is of great guiding significance for identifying the types of PHCZs that need to be monitored and controlled in the environment, as well as for the human health risk assessment of PHCZs.
|
Received: 25 May 2024
|
|
|
|
|
[1] Jia Y X, Cheng J, Sun H F, et al. Sediment-water distribution and potential sources of polyhalogenated carbazoles in a coastal river locating at a north metropolis, China [J]. Marine Pollution Bulletin, 2023,189:114790. [2] Yue S Q, Zhang T, Shen Q Q, et al. Assessment of endocrine-disrupting effects of emerging polyhalogenated carbazoles (PHCZs): In vitro, in silico, and in vivo evidence [J]. Environment International, 2020,140:105729. [3] Wang X, Hu M Y, Li M H, et al. Effects of exposure to 3,6-DBCZ on neurotoxicity and AhR pathway during early life stages of zebrafish (Danio rerio) [J]. Ecotoxicology and Environmental Safety, 2024, 270:115892. [4] Du Z K, Hou K X, Zhou T T, et al. Polyhalogenated carbazoles (PHCZs) induce cardiotoxicity and behavioral changes in zebrafish at early developmental stages [J]. Science of the Total Environment, 2022,841:156738. [5] Kuehl D W, Durhan E, Butterworth B C, et al. Tetrachloro-9H-carbazole, a previously unrecognized contaminant in sediments of the Buffalo River [J]. Journal of Great Lakes Research, 1984,10(2):210-214. [6] Sun Y X, Yang L L, Zheng M H, et al. Industrial source identification of polyhalogenated carbazoles and preliminary assessment of their global emissions [J]. Nature Communications, 2023,14(1):3740. [7] Ji C Y, Chen D, Zhao M R. Environmental behavior and safety of polyhalogenated carbazoles (PHCZs): A review [J]. Environmental Pollution, 2021,268(Part A):115717. [8] Liu M K, Jia Y X, Cui Z L, et al. Occurrence and potential sources of polyhalogenated carbazoles in farmland soils from the Three Northeast Provinces, China [J]. Science of the Total Environment, 2021,799: 149459. [9] 潘永强.浙江省土壤中多卤代咔唑类化合物的时空分布 [D]. 杭州:浙江工业大学, 2018. Pan Y Q. Spatial and temporal of distribution of polyhalogenated carbazoles in soils from Zhejiang Province [D]. Hangzhou: Zhejiang University of Technology, 2018. [10] 孙红斐,柯润辉,王 哲,等.长江口平原农田土壤中卤代咔唑的分布特征及毒性效应 [J]. 生态毒理学报, 2024,19(2):262-271. Sun H F, Ke R H, Wang Z, et al. Distribution characteristics and toxic effects of polyhalogenated carbazoles in agricultural soils of the Yangtze River estuary plains [J]. Asian Journal of Ecotoxicology, 2024, 19(2):262-271. [11] Tao W Q, Zhou Z G, Shen L, et al. Determination of polyhalogenated carbazoles in soil using gas chromatography-triple quadrupole tandem mass spectrometry [J]. Science of the Total Environment, 2020,710: 135524. [12] Liu M K, Huang L H, Li X H, et al. Occurrence and distribution of polyhalogenated carbazoles in eastern Tibetan Plateau soils along the slope of Mt. Qionglai [J]. Chemosphere, 2022,298:134200. [13] Ma J C, Yang B, Hu X J, et al. The binding mechanism of benzophenone-type UV filters and human serum albumin: The role of site, number, and type of functional group substitutions [J]. Environmental Pollution, 2023,324:121342. [14] Li N, Yang X, Chen F P, et al. Spectroscopic and in silico insight into the interaction between dicofol and human serum albumin [J]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2022,264:120277. [15] Rabbani G, Ahn S N. Structure, enzymatic activities, glycation and therapeutic potential of human serum albumin: A natural cargo [J]. International Journal of Biological Macromolecules, 2019,123:979-990. [16] Miles A J, Ramalli S G, Wallace B A. DichroWeb, a website for calculating protein secondary structure from circular dichroism spectroscopic data [J]. Protein Science, 2021,31(1):37-46. [17] Whitmore L, Wallace B A. DICHROWEB, an online server for protein secondary structure analyses from circular dichroism spectroscopic data [J]. Nucleic Acids Research, 2004,32:668-673. [18] Whitmore L, Wallace B A. Protein secondary structure analyses from circular dichroism spectroscopy: Methods and reference databases [J]. Biopolymers, 2008,89(5):392-400. [19] Kumari R, Kumar R, Lynn A. G_mmpbsa-a GROMACS tool for high-throughput MM-PBSA calculations [J]. Journal of Chemical Information and Modeling, 2014,54(7):1951-1962. [20] Zhang F, Zhang J, Tong C L, et al. Molecular interactions of benzophenone UV filters with human serum albumin revealed by spectroscopic techniques and molecular modeling [J]. Journal of Hazardous Materials, 2013,263:618-626. [21] Zargar S, Wani T A. Exploring the binding mechanism and adverse toxic effects of persistent organic pollutant (dicofol) to human serum albumin: A biophysical, biochemical and computational approach [J]. Chemico-Biological Interactions, 2021,350:109707. [22] Kheirdoosh F, Kashanian S, Khodaei M M, et al. Spectroscopic studies on the interaction of aspartame with human serum albumin [J]. Nucleosides, Nucleotides & Nucleic Acids, 2021,40(3):300-316. [23] Dolatabadi J E N, Panahi-Azar V, Barzegar A, et al. Spectroscopic and molecular modeling studies of human serum albumin interaction with propyl gallate [J]. RSC Advances, 2014,4(10):64559-64564. [24] Xu L, Yang H T, Hu R X, et al. Comparing the interaction of four structurally similar coumarins from Fraxinus Chinensis Roxb. with HSA through multi-spectroscopic and docking studies [J]. Journal of Molecular Liquids, 2021,340:117234. [25] Sreedevi S M, Vinod S M, Krishnan A, et al. Molecular docking approach on the effect of site-selective and site-specific drugs on the molecular interactions of human serum albumin (HSA)-acridinedione dye complex [J]. Arabian Journal of Chemistry, 2023,16,104701. [26] Tan S W, Chi Z X, Shan Y, et al. Interaction studies of polybrominated diphenyl ethers (PBDEs) with human serum albumin (HSA): Molecular docking investigations [J]. Environmental Toxicology and Pharmacology, 2017,54:34-39. [27] Sekar G, Haldar M, Kumar D T, et al. Exploring the interaction between iron oxide nanoparticles (IONPs) and human serum albumin (HSA): Spectroscopic and docking studies [J]. Journal of Molecular Liquids, 2017,241:793-800. [28] Ma J C, Qin C, Waigi M G, et al. Functional group substitutions influence the binding of benzophenone-type UV filters with DNA [J]. Chemosphere, 2022,299:134490. |
|
|
|