| Literature DB >> 29287145 |
Yi Yuan1, Chong Du1,2, Cuiji Sun1, Jin Zhu1, Shan Wu3, Yinlong Zhang1,4, Tianjiao Ji1, Jianlin Lei3, Yinmo Yang2, Ning Gao3,5, Guangjun Nie1,6.
Abstract
The targeted delivery of hydrophobic therapeutic drugs to tumors is one of the major challenges in drug development. The use of natural proteins as drug delivery vehicles holds great promise due to various functionalities of proteins. In the current study, we exploited a natural protein, GroEL, which possesses a double layer cage structure, as a hydrophobic drug container, which is switchable by ATP binding to a hydrophilic status, to design a novel and intelligent hydrophobic drug delivery molecular machine with a controlled drug release profile. When loaded with the hydrophobic antitumor drug, Doxorubicin (Dox), GroEL was able to shield the drug from the aqueous phase of blood, releasing the drug once in the presence of a critical concentration of ATP at the tumor site. Unexpectedly, we found that GroEL has a specific affinity for the cell structural protein, plectin, which is expressed at abnormally elevated levels on the membranes of tumor cells but not in normal cells. This finding, in combination with the ATP sensitivity, makes GroEL a superior natural tumor targeting nanocarrier. Our data show that GroEL-Dox is able to effectively, and highly selectively, deliver the hydrophobic drug to fast growing tumors without overt adverse effects on the major organs. GroEL is therefore a promising drug delivery platform that can overcome the obstacles to hydrophobic drug targeting and delivery.Entities:
Keywords: ATP excitation; Chaperonin; GroEL; hydrophobic drug delivery; nanocarrier; tumor targeting
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Year: 2018 PMID: 29287145 DOI: 10.1021/acs.nanolett.7b04307
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189