细胞内
生物结合
化学
生物化学
细胞
氨基酸
药物输送
蛋白质工程
靶蛋白
计算生物学
配体(生物化学)
蛋白质-蛋白质相互作用
细胞生物学
膜蛋白
血浆蛋白结合
细胞膜
蛋白质生物合成
生物
转运蛋白
作者
Wilfred Chen,Millicent O. Sullivan
标识
DOI:10.1007/978-1-0716-3469-1_11
摘要
Protein drugs are a critically important therapeutic modality due to the sophisticated binding recognition, catalytic properties, and disease relevance of proteins. There is a clear need for new strategies able to improve pharmacokinetics, bioavailability, and/or intracellular delivery of therapeutic proteins, as stability limitations have significantly hindered clinical advancement, and most proteins are membrane impermeable. Bioconjugation strategies able to site-specifically modify proteins with cell binding, and other ligands offer a particularly valuable approach to facilitate protein delivery due to the importance of ligand presentation on protein bioactivity and cellular uptake. We explored unnatural amino acid (UAA) incorporation as a novel strategy to tunably incorporate clustered cell-binding ligands in fluorescent proteins and suicide enzymes, resulting in substantial increases in cell-specific uptake and targeted cell-killing activity. These approaches offer a valuable and versatile method to modify a variety of proteins and enable improved clinical potential.
科研通智能强力驱动
Strongly Powered by AbleSci AI