Rapid modification of retroviruses using lipid conjugates
Methods are needed to manipulate natural nanoparticles. Viruses are particularly interesting because they can act as therapeutic cellular delivery agents. Here we examine a new method for rapidly modifying retroviruses that uses lipid conjugates composed of a lipid anchor (1,2-distearoyl-sn-glycero-...
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Published in | Nanotechnology Vol. 20; no. 6; pp. 065103 - 065103 (10) |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
IOP Publishing
11.02.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Methods are needed to manipulate natural nanoparticles. Viruses are particularly interesting because they can act as therapeutic cellular delivery agents. Here we examine a new method for rapidly modifying retroviruses that uses lipid conjugates composed of a lipid anchor (1,2-distearoyl-sn-glycero-3-phosphoethanolamine), a polyethylene glycol chain, and biotin. The conjugates rapidly and stably modified retroviruses and enabled them to bind streptavidin. The implication of this work for modifying viruses for gene therapy and vaccination protocols is discussed. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0957-4484 1361-6528 |
DOI: | 10.1088/0957-4484/20/6/065103 |