We describe an optical biosensor for lysine based on the use of lysine decarboxylase and an optical transducer for detection of cadaverine which is formed as a result of enzymatic action. A plasticized PVC (polyvinyl chloride) membrane containing a lipophilic tartrate as the amine carrier acts as th
A model system for the development of an optical biosensor based on lipid membranes and membrane-bound receptors
โ Scribed by B. Klee; G.L. Duveneck; P. Oroszlan; M. Ehrat; H.M. Widmer
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 451 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0925-4005
No coin nor oath required. For personal study only.
โฆ Synopsis
The reproducible and easy immobilization of receptors on sensor surfaces is a prerequisite for the development of receptor-based fibre optic biosensors. Using a fused silica fiber as the transducer, binding processes of luminescently labeled ligands can be monitored by evanescent wave sensor (EWS) technology. The vesicle fusion technique was chosen for the immobilization of membrane-bound receptors in order to preserve their binding specificity and activity, by embedding them in an environment similar to a lipid bilayer. The results of initial studies of repetitive cycles of lipid layer deposition and removal, indicating good reproducibility of lipid layer formation on the fiber, are presented. Using the binding of ftuorescently labeled streptavidin to a biotinylated lipid layer as a model system for receptor-ligand interaction, good sensitivity, combined with low non-specific binding were observed.
๐ SIMILAR VOLUMES
Secretory phospholipase A 2 (sPLA 2 ) belongs to a family of small interfacially active enzymes that catalyze the hydrolysis of phospholipids, yielding lysolipids and fatty acids. sPLA 2 is found in snake and bee venom and also in inflammatory and cancerous tissue. It is mainly active on organized l
A radiochemical microassay for soluble and membrane-bound glutamate decarboxylase (GAD) is described. Up to 180 samples can be determined per day with a variation coefficient of 2%. The method detects newly synthesized gamma-amino-n-butyric acid in the picomole range and can easily be applied to oth