Vanessa V Gwenin, Chris D Gwenin, Maher Kalaji
Index: Langmuir 27(23) , 14300-7, (2011)
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Directed enzyme prodrug therapy is an extensive area of research in cancer chemotherapy. Although very promising, the current directed approaches are still hampered by inefficient enzyme expression and tumor targeting. This work investigates the viability of using metal nanoparticles as a novel delivery vehicle for prodrug-activating enzymes. Using genetically incorporated amino acid sequences, a nitroreductase from E. coli was directly immobilized onto a 50 nm gold colloid, as confirmed by gel electrophoresis, DLS, and UV-vis spectroscopy. The resulting conjugates showed excellent stability in changing proton and sodium chloride environments, including PBS at 37 °C. Remarkably, the immobilized nitroreductase retained more than 99% activity to the CB1954 prodrug without the need for stabilizers. This work provides the foundation for attaching prodrug-activating enzymes to metal nanoparticles for future use in directed enzyme prodrug therapy.© 2011 American Chemical Society
Structure | Name/CAS No. | Molecular Formula | Articles |
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CB 1954
CAS:21919-05-1 |
C9H8N4O5 |
An unusually cold active nitroreductase for prodrug activati...
2012-06-01 [Bioorg. Med. Chem. 20(11) , 3540-50, (2012)] |
uvrB gene deletion enhances SOS chromotest sensitivity for n...
2010-10-01 [J. Biotechnol. 150(1) , 190-4, (2010)] |
CB 1954: from the Walker tumor to NQO2 and VDEPT.
2003-01-01 [Curr. Pharm. Des. 9(26) , 2091-104, (2003)] |
Antivector and tumor immune responses following adenovirus-d...
2009-11-01 [Hum. Gene Ther. 20(11) , 1249-58, (2009)] |
Insights into the redox cycle of human quinone reductase 2.
2011-10-01 [Free Radic. Res. 45(10) , 1184-95, (2011)] |
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