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4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin

4-Chloro-1,2-phenylenediamine (4-Cl-OPD) is a halogenated aromatic diamine used as a precursor in permanent hair color production. Despite its well-documented mutagenic and carcinogenic effects in various in vitro and in vivo models, its role in fibrillar aggregate formation and their genotoxic effe...

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Autores principales: Warsi, Mohd Sharib, Habib, Safia, Talha, Mohd, Khan, Shifa, Singh, Priyam, Mir, Abdul Rouf, Abidi, Minhal, Ali, Asif, Moinuddin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527296/
https://www.ncbi.nlm.nih.gov/pubmed/36199663
http://dx.doi.org/10.3389/fchem.2022.1016354
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author Warsi, Mohd Sharib
Habib, Safia
Talha, Mohd
Khan, Shifa
Singh, Priyam
Mir, Abdul Rouf
Abidi, Minhal
Ali, Asif
Moinuddin,
author_facet Warsi, Mohd Sharib
Habib, Safia
Talha, Mohd
Khan, Shifa
Singh, Priyam
Mir, Abdul Rouf
Abidi, Minhal
Ali, Asif
Moinuddin,
author_sort Warsi, Mohd Sharib
collection PubMed
description 4-Chloro-1,2-phenylenediamine (4-Cl-OPD) is a halogenated aromatic diamine used as a precursor in permanent hair color production. Despite its well-documented mutagenic and carcinogenic effects in various in vitro and in vivo models, its role in fibrillar aggregate formation and their genotoxic effect in therapeutic proteins has received less attention. The significance of human serum albumin (HSA) arises from its involvement in bio-regulatory and transport processes. HSA misfolding and aggregation are responsible for some of the most frequent neurodegenerative disorders. We used various complementary approaches to track the formation of amyloid fibrils and their genotoxic effect. Molecular dynamics study demonstrated the complex stability. The impact of 4-Cl-OPD on the structural dynamics of HSA was confirmed by Raman spectroscopy, X-ray diffraction, HPLC and SDS-PAGE. Fibrilllar aggregates were investigated using Congo red assay, DLS, and SEM. The genotoxic nature of 4-Cl-OPD was confirmed using plasmid nicking assay and DAPI staining, which revealed DNA damage and cell apoptosis. 4-Cl-OPD provides a model system for studying fibrillar aggregation and their genotoxic potential in the current investigation. Future studies should investigate the inhibition of the aggregation/fibrillation process, which may yield valuable clinical insights.
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spelling pubmed-95272962022-10-04 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin Warsi, Mohd Sharib Habib, Safia Talha, Mohd Khan, Shifa Singh, Priyam Mir, Abdul Rouf Abidi, Minhal Ali, Asif Moinuddin, Front Chem Chemistry 4-Chloro-1,2-phenylenediamine (4-Cl-OPD) is a halogenated aromatic diamine used as a precursor in permanent hair color production. Despite its well-documented mutagenic and carcinogenic effects in various in vitro and in vivo models, its role in fibrillar aggregate formation and their genotoxic effect in therapeutic proteins has received less attention. The significance of human serum albumin (HSA) arises from its involvement in bio-regulatory and transport processes. HSA misfolding and aggregation are responsible for some of the most frequent neurodegenerative disorders. We used various complementary approaches to track the formation of amyloid fibrils and their genotoxic effect. Molecular dynamics study demonstrated the complex stability. The impact of 4-Cl-OPD on the structural dynamics of HSA was confirmed by Raman spectroscopy, X-ray diffraction, HPLC and SDS-PAGE. Fibrilllar aggregates were investigated using Congo red assay, DLS, and SEM. The genotoxic nature of 4-Cl-OPD was confirmed using plasmid nicking assay and DAPI staining, which revealed DNA damage and cell apoptosis. 4-Cl-OPD provides a model system for studying fibrillar aggregation and their genotoxic potential in the current investigation. Future studies should investigate the inhibition of the aggregation/fibrillation process, which may yield valuable clinical insights. Frontiers Media S.A. 2022-09-19 /pmc/articles/PMC9527296/ /pubmed/36199663 http://dx.doi.org/10.3389/fchem.2022.1016354 Text en Copyright © 2022 Warsi, Habib, Talha, Khan, Singh, Mir, Abidi, Ali and Moinuddin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Warsi, Mohd Sharib
Habib, Safia
Talha, Mohd
Khan, Shifa
Singh, Priyam
Mir, Abdul Rouf
Abidi, Minhal
Ali, Asif
Moinuddin,
4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title_full 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title_fullStr 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title_full_unstemmed 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title_short 4-Chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
title_sort 4-chloro-1,2-phenylenediamine induced structural perturbation and genotoxic aggregation in human serum albumin
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527296/
https://www.ncbi.nlm.nih.gov/pubmed/36199663
http://dx.doi.org/10.3389/fchem.2022.1016354
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