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Main Authors: Huang, Yichao, He, Qian, Zhang, Peipei, Song, Juxingsi, Wang, Yangkai, Zhu, Shaoqian, Lv, Yongfei, Zhou, Dayuan, Hu, Yanan, Zhang, Liming, Liu, Guoyan, Wang, Qianqian
Format: Artículo científico
Language:en
Published: Journal of photochemistry and photobiology. B, Biology 2025
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Online Access:https://pubmed.ncbi.nlm.nih.gov/39922038/
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author Huang, Yichao
He, Qian
Zhang, Peipei
Song, Juxingsi
Wang, Yangkai
Zhu, Shaoqian
Lv, Yongfei
Zhou, Dayuan
Hu, Yanan
Zhang, Liming
Liu, Guoyan
Wang, Qianqian
author_facet Huang, Yichao
He, Qian
Zhang, Peipei
Song, Juxingsi
Wang, Yangkai
Zhu, Shaoqian
Lv, Yongfei
Zhou, Dayuan
Hu, Yanan
Zhang, Liming
Liu, Guoyan
Wang, Qianqian
Huang, Yichao
He, Qian
Zhang, Peipei
Song, Juxingsi
Wang, Yangkai
Zhu, Shaoqian
Lv, Yongfei
Zhou, Dayuan
Hu, Yanan
Zhang, Liming
Liu, Guoyan
Wang, Qianqian
collection PubMed - marine biology
contents Single amino acid substitution analogs of marine antioxidant peptides with membrane permeability exert a marked protective effect against ultraviolet-B induced damage. Huang, Yichao He, Qian Zhang, Peipei Song, Juxingsi Wang, Yangkai Zhu, Shaoqian Lv, Yongfei Zhou, Dayuan Hu, Yanan Zhang, Liming Liu, Guoyan Wang, Qianqian Ultraviolet Rays Humans Antioxidants Peptides Oxidative Stress Apoptosis Cell Membrane Permeability HaCaT Cells Cell Survival Glutathione Reactive Oxygen Species NF-E2-Related Factor 2 Keratinocytes Ultraviolet-B (UVB) causes oxidative stress, which is implicated in skin damage and photoaging. Antioxidant peptides exhibit protective effects against UVB-induced oxidative stress and are thus regarded as potential competitors compared to synthetic antioxidants for cosmetics. In the present study, we provided a discovery pipeline for screening and modifying marine-derived antioxidant peptides, and successfully identified and characterized three novel modified peptides (WP5, LW5 and YY6) with strong antioxidant abilities. Their scavenging activities on 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate) radical (ABTS·) and hydroxyl radical (·OH) were higher than those of glutathione (GSH) (ABTS·: 71.12 ± 3.58 %, 67.63 ± 1.65 % and 68.51 ± 0.54 % by WP5, LW5 and YY6, respectively, vs 61.51 ± 1.02 % by GSH; ·OH: 52.15 ± 1.99 %, 51.25 ± 1.29 % and 53.06 ± 2.23 % by WP5, LW5 and YY6, respectively, vs 42.69 ± 1.18 % by GSH). The modified peptides can effectively penetrate cell membrane and significantly enhance cell viability against UVB-induced oxidative stress in human keratinocyte (HaCaT) cells by reducing the levels of reactive oxygen species and malondialdehyde and increasing the activity of intracellular antioxidant enzymes, including superoxide dismutase and glutathione peroxidase. Additionally, the modified peptides decreased the expression of tumor necrosis factor-α, interleukin-6 and interleukin-1β in UVB-induced cell inflammatory response, exhibiting a potent anti-inflammatory activity. Further investigation into the molecular mechanism revealed that the modified peptides not only decreased cell apoptosis by down-regulating the apoptosis factors Bax/Bcl-2 and c-PARP, but also increased the antioxidant capacity of HaCaT cells by interrupting the interaction between Kelch-like ECH associated protein 1 (Keap1) and nuclear factor erythroid 2-related factor 2 (Nrf2), and ultimately promoting Nrf2 activation. The findings suggest a promising strategy for accelerating the discovery of antioxidant peptides and cell-penetrating peptides, providing valuable insights for pharmaceutical and cosmetic industries.
format Artículo científico
id pubmed_39922038
institution PubMed
language en
publishDate 2025
publisher Journal of photochemistry and photobiology. B, Biology
record_format pubmed
spellingShingle Single amino acid substitution analogs of marine antioxidant peptides with membrane permeability exert a marked protective effect against ultraviolet-B induced damage.
Huang, Yichao
He, Qian
Zhang, Peipei
Song, Juxingsi
Wang, Yangkai
Zhu, Shaoqian
Lv, Yongfei
Zhou, Dayuan
Hu, Yanan
Zhang, Liming
Liu, Guoyan
Wang, Qianqian
Ultraviolet Rays
Humans
Antioxidants
Peptides
Oxidative Stress
Apoptosis
Cell Membrane Permeability
HaCaT Cells
Cell Survival
Glutathione
Reactive Oxygen Species
NF-E2-Related Factor 2
Keratinocytes
Single amino acid substitution analogs of marine antioxidant peptides with membrane permeability exert a marked protective effect against ultraviolet-B induced damage. Huang, Yichao He, Qian Zhang, Peipei Song, Juxingsi Wang, Yangkai Zhu, Shaoqian Lv, Yongfei Zhou, Dayuan Hu, Yanan Zhang, Liming Liu, Guoyan Wang, Qianqian Ultraviolet Rays Humans Antioxidants Peptides Oxidative Stress Apoptosis Cell Membrane Permeability HaCaT Cells Cell Survival Glutathione Reactive Oxygen Species NF-E2-Related Factor 2 Keratinocytes Ultraviolet-B (UVB) causes oxidative stress, which is implicated in skin damage and photoaging. Antioxidant peptides exhibit protective effects against UVB-induced oxidative stress and are thus regarded as potential competitors compared to synthetic antioxidants for cosmetics. In the present study, we provided a discovery pipeline for screening and modifying marine-derived antioxidant peptides, and successfully identified and characterized three novel modified peptides (WP5, LW5 and YY6) with strong antioxidant abilities. Their scavenging activities on 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate) radical (ABTS·) and hydroxyl radical (·OH) were higher than those of glutathione (GSH) (ABTS·: 71.12 ± 3.58 %, 67.63 ± 1.65 % and 68.51 ± 0.54 % by WP5, LW5 and YY6, respectively, vs 61.51 ± 1.02 % by GSH; ·OH: 52.15 ± 1.99 %, 51.25 ± 1.29 % and 53.06 ± 2.23 % by WP5, LW5 and YY6, respectively, vs 42.69 ± 1.18 % by GSH). The modified peptides can effectively penetrate cell membrane and significantly enhance cell viability against UVB-induced oxidative stress in human keratinocyte (HaCaT) cells by reducing the levels of reactive oxygen species and malondialdehyde and increasing the activity of intracellular antioxidant enzymes, including superoxide dismutase and glutathione peroxidase. Additionally, the modified peptides decreased the expression of tumor necrosis factor-α, interleukin-6 and interleukin-1β in UVB-induced cell inflammatory response, exhibiting a potent anti-inflammatory activity. Further investigation into the molecular mechanism revealed that the modified peptides not only decreased cell apoptosis by down-regulating the apoptosis factors Bax/Bcl-2 and c-PARP, but also increased the antioxidant capacity of HaCaT cells by interrupting the interaction between Kelch-like ECH associated protein 1 (Keap1) and nuclear factor erythroid 2-related factor 2 (Nrf2), and ultimately promoting Nrf2 activation. The findings suggest a promising strategy for accelerating the discovery of antioxidant peptides and cell-penetrating peptides, providing valuable insights for pharmaceutical and cosmetic industries.
title Single amino acid substitution analogs of marine antioxidant peptides with membrane permeability exert a marked protective effect against ultraviolet-B induced damage.
topic Ultraviolet Rays
Humans
Antioxidants
Peptides
Oxidative Stress
Apoptosis
Cell Membrane Permeability
HaCaT Cells
Cell Survival
Glutathione
Reactive Oxygen Species
NF-E2-Related Factor 2
Keratinocytes
url https://pubmed.ncbi.nlm.nih.gov/39922038/