Abstract
A non-labeling fluorescence sensor system was developed using polydiacetylene (PDA) liposomes composed of 10,12-pentacosadiynoic acid (PCDA) and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) at a 8:2 molar ratio. The PDA liposomes were immobilized onto an amine-coated glass surface using peptide bonding between the carboxyl group of the liposome and the amine group of the glass surface. The optimum ratio of the cross linker (NHS/EDC) to PDA liposome was determined to be 50% for strong immobilization of the liposomes. Residual carboxyl groups of the PDA liposomes were selectively biotinylated, followed by sequential binding of streptavidin and biotin-antibody (bioreceptor). Finally, the performance of the PDA liposome chip was tested for detecting Cryptosporidium parvum, and yielded a detection limit of 1 × 103 oocysts/mL. From these results, it is expected that the PDA liposome chip will have high application potential for the detection of waterborne pathogens including C. Parvum.
Original language | English |
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Pages (from-to) | 687-693 |
Number of pages | 7 |
Journal | Biotechnology Journal |
Volume | 3 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2008 May |
Externally published | Yes |
Keywords
- Cryptosporidium parvum
- Fluorescence chip
- Immobilization
- Liposome
- Polydiacetylene
ASJC Scopus subject areas
- Applied Microbiology and Biotechnology
- Molecular Medicine