| Literature DB >> 26249533 |
Hirotaka Nakatsuji1, Tomohiro Numata2, Nobuhiro Morone3, Shuji Kaneko4, Yasuo Mori2, Hiroshi Imahori3,1, Tatsuya Murakami5.
Abstract
Controlling cell functions using external photoresponsive nanomaterials has enormous potential for the development of cell-engineering technologies and intractable disease therapies, but the former currently requires genetic modification of the target cells. We present a method using plasma-membrane-targeted gold nanorods (pm-AuNRs) prepared with a cationic protein/lipid complex to activate a thermosensitive cation channel, TRPV1, in intact neuronal cells. Highly localized photothermal heat generation mediated by the pm-AuNRs induced Ca(2+) influx solely by TRPV1 activation. In contrast, the use of previously reported cationic AuNRs that are coated with a conventional synthetic polymer also led to photoinduced Ca(2+) influx, but this influx resulted from membrane damage. Our method provides an optogenetic platform without the need for prior genetic engineering of the target cells and might be useful for novel TRPV1-targeted phototherapeutic approaches.Entities:
Keywords: cell engineering; ion channels; nanoparticles; photothermal effects; surface chemistry
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Year: 2015 PMID: 26249533 DOI: 10.1002/anie.201505534
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336