化学
胶束
组合化学
两亲性
聚合物
体内分布
生物物理学
共聚物
有机化学
生物化学
体外
水溶液
生物
作者
Qiangqiang Shi,Hao Yin,Rundi Song,Jie Xu,Jiajia Tan,Xin Zhou,Jie Cen,Zhengyu Deng,Huimin Tong,Chenhui Cui,Yanfeng Zhang,Xiaopeng Li,Zhengbiao Zhang,Shiyong Liu
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2022-11-03
卷期号:15 (2): 257-270
被引量:61
标识
DOI:10.1038/s41557-022-01076-y
摘要
Identification and quantification of synthetic polymers in complex biological milieu are crucial for delivery, sensing and scaffolding functions, but conventional techniques based on imaging probe labellings only afford qualitative results. Here we report modular construction of precise sequence-defined amphiphilic polymers that self-assemble into digital micelles with contour lengths strictly regulated by oligourethane sequences. Direct sequence reading is accomplished with matrix-assisted laser desorption/ionization (MALDI) tandem mass spectrometry, facilitated by high-affinity binding of alkali metal ions with poly(ethylene glycol) dendrons and selective cleavage of benzyl-carbamate linkages. A mixture of four types of digital micelles could be identified, sequence-decoded and quantified by MALDI and MALDI imaging at cellular, organ and tissue slice levels upon in vivo administration, enabling direct comparison of biological properties for each type of digital micelle in the same animal. The concept of digital micelles and encoded amphiphiles capable of direct sequencing and high-throughput label-free quantification could be exploited for next-generation precision nanomedicine designs (such as digital lipids) and protein corona studies.
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