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Binding Mechanism of Nitro Musks to Human Lactoferrin: Multispectral Approach, Docking and Molecular Dynamics Simulation.
Li, Zemeng; Shi, Mengjie; Liu, Hongyan; Yi, Zhongsheng; Mo, Lingyun; Jiang, Tiemin.
Afiliación
  • Li Z; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, 541004, China.
  • Shi M; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, 541004, China.
  • Liu H; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, 541004, China.
  • Yi Z; South Asia Branch of National Engineering Center of Dairy for Maternal and Child Health, Guilin University of Technology, Guilin, 541004, China.
  • Mo L; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, 541004, China.
  • Jiang T; College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, 541004, China.
Chem Biodivers ; : e202401610, 2024 Aug 28.
Article en En | MEDLINE | ID: mdl-39195350
ABSTRACT
Nitro musks are highly bioaccumulative and potentially carcinogenic, commonly used as additives in fabric softeners, detergents, and other household products. Furthermore, these substances have been detected in breast milk and human adipose tissue, posing a risk of direct exposure to pregnant women and infants. Human lactoferrin (HLF) is abundant in colostrum, and plays an important role in the non-specific immune system of the human body. In this study, the mechanisms of action of two nitro musk compounds, typical examples of synthetic musks, with HLF were investigated using molecular docking, dynamics simulation and multispectral methods. The fluorescence findings demonstrated that nitro musks quenched the intrinsic fluorescence of human lactoferrin through static quenching. Thermodynamic analysis of the binding parameters suggested that hydrophobic interactions acted synergistically in the formation of the complex. Moreover, analyses utilizing multispectral techniques, such as Fourier transform infrared (FTIR) spectroscopy, validated that the microenvironment and structure of HLF were altered in the presence of nitro musks. Finally, molecular docking and molecular dynamics simulations were employed to explore the specific binding mode of nitro musks with HLF and to assess the stability of the complex. These findings may provide a reference for assessing health risks to pregnant women and infants.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China
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