Detection of liposome lysis utilizing an enzyme-substrate system
Autor: | Aysegul Aygun, Daniel J. Wichelecki, Trisha M. McNew, Larry D. Stephenson, Kathryn Torrey |
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Rok vydání: | 2010 |
Předmět: |
Lysis
Octoxynol Drug Compounding Bioengineering Applied Microbiology and Biotechnology Biochemistry Nitrophenols Beta-galactosidase Molecular Biology chemistry.chemical_classification Drug compounding Liposome Chromatography biology Chemistry Hydrolysis General Medicine Nitrophenylgalactosides beta-Galactosidase Fluorescence Enzyme Spectrophotometry Liposomes biology.protein Microscopy Electron Scanning Indicators and Reagents Biotechnology |
Zdroj: | Applied biochemistry and biotechnology. 165(2) |
ISSN: | 1559-0291 |
Popis: | A novel optical reporter system was developed to verify encapsulation and subsequent release of a foreign molecule in liposomes. The protocol utilizes a single enzyme and substrate. We encapsulate o-nitrophenyl-β,D: -galactopyranoside (ONPG) and measure its release by detecting the levels of o-nitrophenol created when the encapsulated ONPG is released and hydrolyzed by β-galactosidase. Using this method, liposome formation and subsequent lysis with Triton X-100 were verified. This new protocol eliminates the complications of multiple reaction enzyme detection methods, along with the chance for false negatives and unreliable data seen when using fluorescent particles as reporters. |
Databáze: | OpenAIRE |
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