凝聚
材料科学
内在无序蛋白质
纳米技术
胞浆
内化
膜
细胞质
纳米生物技术
内吞作用
限制
细胞器
生物物理学
内体
高分子
同种类的
纳米壳
构象变化
生物相容性材料
膜生物学
聚电解质
蛋白质稳定性
相(物质)
化学
作者
Soyeong Jin,Hyemin Park,Seuk‐Min Ryu,Dagyeong Guk,Jae-Eun Lee,Seongeon Jin,Changjoon Keum,Jinyoung Park,Myoung‐Hwan Park,Chaekyu Kim,Hojun Kim,Jaegeun Noh,Kwan H. Lee,Ja‐Hyoung Ryu,Youngdo Jeong
标识
DOI:10.1002/adma.202507877
摘要
In eukaryotic cells, membraneless organelles (MLOs) are formed via liquid‒liquid phase separation (LLPS) involving intrinsically disordered proteins (IDPs) and biomacromolecules, enabling biomacromolecule transport without vesicles, transporters, or channels. Although MLO-mimetic coacervates generated from synthetic biomaterials can deliver biomacromolecules into cells, they lack the conformational adaptability of IDPs and a defined internalization mechanism, limiting their stability under physiological conditions and hindering biomedical translation. Here, IDP-inspired nanovectors (IDP-NVs) are developed with conformational adaptability capable of forming nanocoacervates (NCs) with biomacromolecules for cytosolic delivery. Mixing with IDP-NVs and cargos results in stable NCs under physiological conditions, and the NCs can directly penetrate cellular membranes through the molecular motion of IDP-NVs. After the internalization, cytoplasmic glutathione triggers NC disassembly, releasing biomacromolecules in the cytosol. The NCs effectively deliver biomacromolecules of diverse sizes, charges, shapes (globular proteins and antibodies), and functions (mRNAs and CRISPR units), demonstrating their versatility and potential for biomedical applications.
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