Fluorescence Lifetime Imaging Microscopy Analysis of Isolated Melanosomes
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arXiv
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| Autori principali: | , , , |
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| Natura: | Preprint |
| Pubblicazione: |
2025
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| _version_ | 1866913938966315008 |
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| author | Kizilov, Mykyta Jung, Sujeong Cheburkanov, Vsevolod Yakovlev, Vladislav V. |
| author_facet | Kizilov, Mykyta Jung, Sujeong Cheburkanov, Vsevolod Yakovlev, Vladislav V. |
| contents | Melanosomes are organelles found in a wide variety of tissues throughout the animal kingdom. They contain a variety of biological molecules, but the dominant constituent is the pigment melanin, and many functions ascribed to melanosomes, such as photoprotection, are uniquely enabled by the chemical properties and structures of the melanins they contain. In this report, we used, for the first time, Fluorescence Lifetime Imaging Microscopy (FLIM) to examine fluorescent properties of pigments in melanosomes and evaluate their time evolution upon extended laser irradiation. We discovered a relatively short-lived component in fluorescence emission and revealed significant changes in lifetimes upon irradiation indicating structural photoinduced changes to melanin occurring on a time scale of minutes, with observations extending up to one hour. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2507_09114 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Fluorescence Lifetime Imaging Microscopy Analysis of Isolated Melanosomes Kizilov, Mykyta Jung, Sujeong Cheburkanov, Vsevolod Yakovlev, Vladislav V. Biological Physics Optics Melanosomes are organelles found in a wide variety of tissues throughout the animal kingdom. They contain a variety of biological molecules, but the dominant constituent is the pigment melanin, and many functions ascribed to melanosomes, such as photoprotection, are uniquely enabled by the chemical properties and structures of the melanins they contain. In this report, we used, for the first time, Fluorescence Lifetime Imaging Microscopy (FLIM) to examine fluorescent properties of pigments in melanosomes and evaluate their time evolution upon extended laser irradiation. We discovered a relatively short-lived component in fluorescence emission and revealed significant changes in lifetimes upon irradiation indicating structural photoinduced changes to melanin occurring on a time scale of minutes, with observations extending up to one hour. |
| title | Fluorescence Lifetime Imaging Microscopy Analysis of Isolated Melanosomes |
| topic | Biological Physics Optics |
| url | https://arxiv.org/abs/2507.09114 |