| Literature DB >> 25352251 |
Kenta Fujita1, Yuya Tanaka, Takeya Sho, Shuichi Ozeki, Satoshi Abe, Tatsuo Hikage, Takahiro Kuchimaru, Shinae Kizaka-Kondoh, Takafumi Ueno.
Abstract
Protein cages have been utilized as templates in the development of biomaterials. Here we report protein engineering of the ferritin (Fr) cage for encapsulating carbon monoxide releasing molecules (CORMs) and release of CO gas which serves as a cell signaling molecule. The protein cages enable us to increase the half-life for CO release, providing a release rate that is 18-fold slower than the rate of a typical CORM, Ru(CO)3Cl(glycinate) (CORM-3). Moreover, the uptake ratio of the composite is about 4-fold greater than that of CORM-3. We found that these effects enhance the activation of nuclear factor κB 10-fold higher than CORM-3. The protein cage of Fr thus provides the basis for new CORMs that can be used for in vitro cell research.Entities:
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Year: 2014 PMID: 25352251 DOI: 10.1021/ja508938f
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419