
Journal of Lipid Research, Год журнала: 2024, Номер unknown, С. 100643 - 100643
Опубликована: Сен. 1, 2024
Язык: Английский
Journal of Lipid Research, Год журнала: 2024, Номер unknown, С. 100643 - 100643
Опубликована: Сен. 1, 2024
Язык: Английский
Journal of Lipid Research, Год журнала: 2024, Номер 65(8), С. 100601 - 100601
Опубликована: Июль 20, 2024
Язык: Английский
Процитировано
4International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(3), С. 889 - 889
Опубликована: Янв. 22, 2025
Due to the lack of measurement techniques suitable for examining compartments intact, living cells, membrane biophysics is almost exclusively investigated in plasma despite fact that its alterations intracellular organelles may also contribute disease pathogenesis. Here, we employ a novel, easy-to-use, confocal microscopy-based approach utilizing F66, an environment-sensitive fluorophore combination with fluorescent organelle markers and quantitative image analysis determine magnitude molecular order-related dipole potential various tumor neural cell lines. Our comparative demonstrates considerable variations be large enough modulate protein functions, inward decreasing gradient on route secretory/endocytic pathway (plasma >> lysosome > Golgi endoplasmic reticulum), whereas mitochondrial membranes are characterized by slightly larger than lysosomes. sensitive quantify biophysical properties selectively their and, therefore, identify affected therapeutic targets diseases associated lipid composition thus such as tumors, metabolic, neurodegenerative, or lysosomal storage disorders.
Язык: Английский
Процитировано
0Advanced Science, Год журнала: 2025, Номер unknown
Опубликована: Фев. 9, 2025
Abstract Mitochondrial membrane environmental dynamics are crucial for understanding function, yet high‐resolution observation remains challenging. Here, HBimmCue is introduced as a fluorescent probe localized to inner mitochondrial (IMM) that reports lipid polarity and order changes, which correlate with cellular respiration levels. Using fluorescence lifetime imaging microscopy (FLIM), IMM heterogeneity uncovered across scales, from nanoscale structures within individual mitochondria mouse pre‐implantation embryos. At the sub‐organelle level, stimulated emission depletion (STED)‐FLIM highlights variations IMM. sub‐cellular reduced observed in damaged marked lysosomal degradation distinct distributions identified neurons disease models. Additionally, metabolic dysfunction associated oocytes aging reprogramming zygote blastocyst detected. Together, work demonstrates broad applicability of HBimmCue, offering new paradigm investigating level at multiple scales.
Язык: Английский
Процитировано
0Frontiers in Cell and Developmental Biology, Год журнала: 2025, Номер 13
Опубликована: Апрель 24, 2025
Язык: Английский
Процитировано
0Journal of Lipid Research, Год журнала: 2024, Номер unknown, С. 100643 - 100643
Опубликована: Сен. 1, 2024
Язык: Английский
Процитировано
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