化学
基因沉默
转铁蛋白受体
肽
内化
受体
小干扰RNA
结合
药物输送
细胞生物学
体内
体外
生物化学
转染
基因
生物
数学分析
生物技术
有机化学
数学
作者
Tiancheng Fu,Fushun Fan,Yingying Lin,Zhenxian Mo,Minhua Zhou,Xiaolan Ye,Xiong Cai,Zaijun Zhang,Changgeng Qian,Xinjian Liu
标识
DOI:10.1021/acs.bioconjchem.5c00225
摘要
Transferrin receptor 1 (TfR1) is a ubiquitously expressed receptor characterized by rapid internalization kinetics and efficient receptor recycling, making it an attractive target for drug delivery. Herein, we investigated the potential of TfR1-binding peptide-siRNA conjugates for central nervous system (CNS)-specific gene silencing. A panel of TfR1-binding peptides and conjugation linkers were synthesized to enable siRNA attachment and evaluate their gene-silencing effects. Conjugation with the hTfR No. 894 peptide achieved effective siRNA delivery both in vitro and in vivo . Compared to ribose 2’- O -hexadecyl (C16)-siRNA conjugates, the hTfR No. 894-siRNA conjugation ( POC2 ) elicited favorable pharmacokinetic characteristics and robust and durable silencing of the target gene across CNS regions following local administration, with minimal impact on peripheral tissues. These findings support TfR1-binding peptide conjugation as a promising strategy for CNS-targeted siRNA delivery.
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