| Literature DB >> 28010059 |
Joanna Macdonald1, Justin Henri1, Lynda Goodman1, Dongxi Xiang1, Wei Duan1, Sarah Shigdar1.
Abstract
The treatment of brain disorders is greatly hindered by the presence of the blood-brain barrier, which restricts the overwhelming majority of small molecules from entering the brain. A novel approach by which to overcome this barrier is to target receptor mediated transport mechanisms present on the endothelial cell membranes. Therefore, we fused an aptamer that binds to epithelial cell adhesion molecule-expressing cancer cells to an aptamer targeting the transferrin receptor. This generated a proof of concept bifunctional aptamer that can overcome the blood-brain barrier and potentially specifically target brain disorders. The initial fusion of the two sequences enhanced the binding affinity of both aptamers while maintaining specificity. Additionally, mutations were introduced into both binding loops to determine their effect on aptamer specificity. The ability of the aptamer to transcytose the blood-brain barrier was then confirmed in vivo following a 1 nmol injection. This study has shown that through the fusion of two aptamer sequences, a bifunctional aptamer can be generated that has the potential to be developed for the specific treatment of brain disorders.Entities:
Keywords: Aptamer; bifunctional; blood−brain barrier; epithelial cell adhesion molecule (EpCAM); receptor mediated transcytosis; transferrin receptor
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Year: 2017 PMID: 28010059 DOI: 10.1021/acschemneuro.6b00369
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418