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MITO-Porter : a liposome-based carrier system for delivery of macromolecules into mitochondria via membrane fusion
Title: | MITO-Porter : a liposome-based carrier system for delivery of macromolecules into mitochondria via membrane fusion |
Authors: | Yamada, Yuma Browse this author →KAKEN DB | Akita, Hidetaka Browse this author | Kamiya, Hiroyuki Browse this author | Kogure, Kentaro Browse this author | Yamamoto, Takenori Browse this author | Shinohara, Yasuo Browse this author | Yamashita, Kikuji Browse this author | Kobayashi, Hideo Browse this author | Kikuchi, Hiroshi Browse this author | Harashima, Hideyoshi Browse this author →KAKEN DB |
Keywords: | non-viral vector | mitochondria | mitochondrial drug delivery | MITO-Porter | membrane fusion | octaarginine |
Issue Date: | Feb-2008 |
Publisher: | Elsevier |
Journal Title: | Biochimica et biophysica acta (BBA). Biomembranes |
Volume: | 1778 |
Issue: | 2 |
Start Page: | 423 |
End Page: | 432 |
Publisher DOI: | 10.1016/j.bbamem.2007.11.002 |
PMID: | 18054323 |
Abstract: | Mitochondria are the principal producers of energy in higher cells. Mitochondrial dysfunction is implicated in a variety of human diseases, including cancer and neurodegenerative disorders. Effective medical therapies for such diseases will ultimately require targeted delivery of therapeutic proteins or nucleic acids to the mitochondria, which will be achieved through innovations in the nanotechnology of intracellular trafficking. Here we describe a liposome-based carrier that delivers its macromolecular cargo to the mitochondrial interior via membrane fusion. These liposome particles, which we call MITO-Porters, carry octaarginine surface modifications to stimulate their entry into cells as intact vesicles (via macropinocytosis). We identified lipid compositions for the MITO-Porter which promote both its fusion with the mitochondrial membrane and the release of its cargo to the intra-mitochondrial compartment in living cells. Thus, the MITO-Porter holds promise as an efficacious system for the delivery of both large and small therapeutic molecules into mitochondria. |
Relation: | http://www.sciencedirect.com/science/journal/00052736 |
Type: | article (author version) |
URI: | http://hdl.handle.net/2115/33806 |
Appears in Collections: | 薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 山田 勇磨
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