Thermosensitive Capturer Coupled with the CD63 Aptamer for Highly Efficient Isolation of Exosomes

适体 低临界溶液温度 微泡 外体 共聚物 材料科学 化学 生物物理学 纳米技术 聚合物 小RNA 分子生物学 生物 生物化学 有机化学 基因
作者
Junjun Yu,Ying Wei,Zepeng Cui,Jia Tian,Haibo Cai,Weian Zhang
出处
期刊:ACS Macro Letters [American Chemical Society]
卷期号:: 195-200 被引量:13
标识
DOI:10.1021/acsmacrolett.3c00682
摘要

Exosomes are bioactive substances secreted by various cells that play a crucial role in cell communication. Due to their nanoscale size and interference from nonexosome proteins, the rapid capture and nondestructive release of exosomes remain a technical challenge which significantly hinders their biomedical application. To overcome this obstacle, we have designed a CD63 aptamer-based thermosensitive copolymer for the effective isolation of exosomes from mesenchymal stem cells (MSCs). A thermal-responsive copolymer, poly( N -isopropylacrylamide- co -butyl methacrylate- co - N -hydroxysuccinimide methacrylate) P(NIPAM- co -BMA- co -NHSMA, PNB), was prepared, which could realize reversible hydrophilic/hydrophobic phase transition by varying temperature. Then, CD63 aptamers were further modified to the copolymer to form the PNB-aptamer, where the aptamer units, acting as a “lock and key”, specifically bind exosomes. Under the low critical solution temperature (LCST) of the PNB-aptamer, it can maintain a hydrophilic state, capturing exosomes from the cell culture medium. Subsequently, exosome-carrying PNB-aptamers can endure from hydrophilic to hydrophobic phase transition by increasing the temperature above its LCST, and then they can be collected after centrifugation. By introducing the complementary sequence of the CD63 aptamer, the stronger binding affinity between the complementary sequence and the aptamers facilitates the release of exosomes from the PNB-aptamer. The yield of exosome samples captured from a MSC culture medium by the PNB-aptamer system (around 62%) is considerably higher than that obtained by the current “gold standard” ultrafiltration (UC) approach (around 42%). Thus, the PNB-aptamer capturer provides a potential strategy for highly efficient exosome isolation.
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