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231224s2017 xx |||||o 00| ||eng c |
| 024 |
7 |
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|a 10.1002/adma.201605604
|2 doi
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|a pubmed25n0895.xml
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|a eng
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| 100 |
1 |
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|a Yang, Yoosoo
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Virus-Mimetic Fusogenic Exosomes for Direct Delivery of Integral Membrane Proteins to Target Cell Membranes
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|c 2017
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| 336 |
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Completed 11.10.2018
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|a Date Revised 30.09.2020
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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|a An efficient system for direct delivery of integral membrane proteins is successfully developed using a new biocompatible exosome-based platform. Fusogenic exosomes harboring viral fusogen, vascular stomatitis virus (VSV)-G protein, can fuse with and modify plasma membranes in a process called "membrane editing." This can facilitate the transfer of biologically active membrane proteins into the target cell membranes both in vitro and in vivo
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|a Journal Article
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|a exosomes
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|a membrane protein
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|a nanoplatform
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|a viral fusogen
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| 650 |
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|a Liposomes
|2 NLM
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| 650 |
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|a Membrane Proteins
|2 NLM
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| 650 |
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|a Viral Proteins
|2 NLM
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| 650 |
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|a Green Fluorescent Proteins
|2 NLM
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|a 147336-22-9
|2 NLM
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|a Polyethylene Glycols
|2 NLM
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|a 3WJQ0SDW1A
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| 700 |
1 |
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|a Hong, Yeonsun
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1 |
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|a Nam, Gi-Hoon
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chung, Jin Hwa
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| 700 |
1 |
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|a Koh, Eunee
|e verfasserin
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| 700 |
1 |
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|a Kim, In-San
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
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|g 29(2017), 13 vom: 06. Apr.
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