MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1021/acs.jmedchem.6c02116

Медицинская библиотека · Journal of medicinal chemistry · 2026

Fluorination-Tuned Ionizable Lipids Regulate Nano-PROTAC Trafficking for Enhanced Targeted Protein Degradation.

Li 李军瑶 Junyao, Min 闵欢 Huan, Song 宋焱 Yan, Huo 霍荣 Rong, Du 杜琳 Lin, Li 李永正 Yongzheng, Du 杜亚静 Yajing, Ding 丁卫 Wei, Zhang 张银龙 Yinlong, Li 李一叶 Yiye, Nie 聂广军 Guangjun, Qi 祁迎秋 Yingqiu

СтатьяПеревод пока не подготовлен

Аннотация

Nanoscale proteolysis-targeting chimeras (nano-PROTACs) offer modular platforms for targeted protein degradcine-rich α-2-glycoprotein 1 (LRG1). i16αCF3-LipoTAC showed greater degradation potend endocytosis, and promoted endosomal escape. In 4T1 tumor models, i16αCF3-LipoTAC prolonged circulation, increased tumor accumulation and target depletion, and improved antitumor efficacy. These findings support fluorination tuning as a strategy to enhance nano-PROTAC trafficking and degradation efficiency.Nanoscale proteolysis-targeting chimeras (nano-PROTACs) offer modular platforms for targeted protein degradcine-rich α-2-glycoprotein 1 (LRG1). i16αCF3-LipoTAC showed greater degradation potend endocytosis, and promoted endosomal escape. In 4T1 tumor models, i16αCF3-LipoTAC prolonged circulation, increased tumor accumulation and target depletion, and improved antitumor efficacy. These findings support fluorination tuning as a strategy to enhance nano-PROTAC trafficking and degradation efficiency.Nanoscale proteolysis-targeting chimeras (nano-PROTACs) offer modular platforms for targeted protein degradcine-rich α-2-glycoprotein 1 (LRG1). i16αCF3-LipoTAC showed greater degradation potend endocytosis, and promoted endosomal escape. In 4T1 tumor models, i16αCF3-LipoTAC prolonged circulation, increased tumor accumulation and target depletion, and improved antitumor efficacy. These findings support fluorination tuning as a strategy to enhance nano-PROTAC trafficking and degradation efficiency.Nanoscale proteolysis-targeting chimeras (nano-PROTACs) offer modular platforms for targeted protein degradcine-rich α-2-glycoprotein 1 (LRG1). i16αCF3-LipoTAC showed greater degradation potend endocytosis, and promoted endosomal escape. In 4T1 tumor models, i16αCF3-LipoTAC prolonged circulation, increased tumor accumulation and target depletion, and improved antitumor efficacy. These findings support fluorination tuning as a strategy to enhance nano-PROTAC trafficking and degradation efficiency.

Для цитирования: Li 李军瑶 Junyao, Min 闵欢 Huan, Song 宋焱 Yan, Huo 霍荣 Rong, Du 杜琳 Lin, Li 李永正 Yongzheng, Du 杜亚静 Yajing, Ding 丁卫 Wei, Zhang 张银龙 Yinlong, Li 李一叶 Yiye, Nie 聂广军 Guangjun, Qi 祁迎秋 Yingqiu. Fluorination-Tuned Ionizable Lipids Regulate Nano-PROTAC Trafficking for Enhanced Targeted Protein Degradation.. Journal of medicinal chemistry. 2026. DOI: 10.1021/acs.jmedchem.6c02116.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.