Hostname: page-component-586b7cd67f-t7fkt Total loading time: 0 Render date: 2024-11-25T15:51:24.875Z Has data issue: false hasContentIssue false

Polydiacetylene Liposomes Attached to Glass Fibers for Fluorescent Bioassays

Published online by Cambridge University Press:  01 February 2011

Mary A Reppy
Affiliation:
[email protected], Analytical Biological Services Inc, Research Division, 701-4 Cornell Business Park, Wilmington, DE, 19801, United States
Bradford A Pindzola
Affiliation:
[email protected], Analytical Biological Services Inc, 701-4 Cornell Business Park, Wilmington, DE, 19801, United States
Get access

Abstract

Polydiacetylene (PDA) is a conjugated polymer that changes its fluorescent state in response to environmental changes and can act as a transducer to convert molecular interactions into a discernable output measurable in the macroscopic world. Energy transfer to fluorophores can further enhance the fluorescent signal. Diacetylene liposomes can be prepared with phospholipids and other cell membrane components in the liposomes, and photopolymerized. PDA liposomes have been used for absorbance based detection of biological targets; however, moving to fluorescence detection gives increased sensitivity and also allows sensing from PDA structures deposited on opaque membranes. Unfortunately, PDA liposomes are prone to aggregation, particularly in the presence of divalent cations. Many enzymes require divalent cations such as Mg2+, Mn2+, Ca2+, etc., as co-factors; the tendency of PDA liposomes to aggregate in the presence of these cations limits their use as a platform for detection of enzymatic activity. We have developed methods for attaching PDA liposomes to glass fiber membranes, via thiol-epoxide coupling chemistry, for use in bio-assays and have seen that these materials can be used in place of PDA liposome solutions. We present here the attachment of PDA liposomes to glass fiber membranes in 96-well format, cryogenic TEM scans of the attached liposomes and the use of these materials in fluorescence assays to detect the activity and inhibition of phospholipase A2.

Type
Research Article
Copyright
Copyright © Materials Research Society 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Okada, S., Peng, S., Spevak, W., Charych, D., Acc. Chem. Res. 1998, 31, 229239.Google Scholar
2 Mu, Z., Li, J., Jiang, L. Langmuir 2000, 16, 78017804.Google Scholar
3 Kolusheva, S., Kafri, R., Jelinek, R. J. Am. Chem. Soc. 2001, 123, 417422.Google Scholar
4 Reppy, M., Sporn, S., Saller, F., U.S. Pat. 6984528,2000 Google Scholar
5 Pindzola, B., Nguyen, A., Reppy, M., Chem. Commun. 2006, 906908.Google Scholar
6 Reppy, M. Mater. Res. Soc. Symp. Proc. 2002, 723, O5:9196.Google Scholar
7 Shim, H., Lee, S., Ahn, D., Ahn, K-D., Kim, J-M Mater. Sci. Eng. C 2004, 24, 157161.Google Scholar
8 Kim, J-M, Lee, Y., Yang, D., Lee, J-S., Lee, G., Ahn, D. J. Am. Chem. Soc. 2005, 127, 1758017581.Google Scholar
9 Hermanson, G. T., “Bioconjugate Techniques,” 1996, Academic Press, London, p142.Google Scholar
10 Okada, S., Jelinek, R., Charych, D. Angew. Chem. Int. Ed. 1999, 38, 655659.Google Scholar
11 Carvalho, M., Jacobs, R. Biochem. Pharm. 1991, 42, 16211626.Google Scholar