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A fiber-optic biosensor was developed for detection of cocaine, its metabolites, and other coca alkaloids, using a monoclonal antibody (mAb) against a derivatized benzoylecgonine (BE). The mAb was immobilized noncovalently on quartz fibers and a flow fluorometer was used to detect changes in evanescent wave fluorescence. A fluorescein (FL) conjugate of BE bound to the mAb specifically in a saturable manner and with high affinity (Kd = 7.6 nM). Cocaine or other test compounds competed with FL-BE for binding to the mAb in a concentration-dependent manner, thereby reducing the initial rate or steady-state fluorescence. Addition of cocaine to the flow buffer after reaching steady-state fluorescence enhanced the dissociation of bound FL-BE, and cocaine removal allowed fiber regeneration for multiple measurements. The detection limits for cocaine, cocaethylene, norcocaine, and BE were 5, 5, 29, and 30 ng/ml, respectively, but for ecgonine it was 4600 ng/ml and for methylecgonine it was 2000 ng/ml. Tropacocaine was detected at 10 ng/ml, but atropine was detected at 2900 ng/ml. The biosensor discriminated by 833-fold between cocaine and its stereoisomer pseudococaine. Structural features necessary for high-affinity recognition by this mAb are benzoate and 3 beta configuration, both of which are found in BE, cocaine, norcocaine, and cocaethylene.

The nicotinic acetylcholine receptor, purified from Torpedo electric organ, was coupled to a light addressable potentiometric sensor (LAPS) to form a LAPS-receptor biosensor. Receptor-ligand complexes containing biotin and urease were captured on a biotinylated nitrocellulose membrane via a streptavidin bridge and detected with a silicon-based sensor. Competition between biotinylated α-bungarotoxin and nonbiotinylated ligands formed the basis of this assay. This biosensor detected both agonists (acetylcholine, carbamylcholine, succinylcholine, suberyldicholine, and nicotine) and competitive antagonists ( d -tubocurarine, α-bungarotoxin, and α- Naja toxin) of the receptor with affinities comparable to those obtained using radioactive ligand binding assays. Consistent with agonist-induced desensitization of the receptor, the LAPS-receptor biosensor reported a time-dependent increase in affinity for the agonist carbamylcholine as expected, but not for the antagonists.

Electrofocusing followed by chromatography on Sephadex G-50 proved to be a fast method for the purification of the neurotoxin, α-bungarotoxin (α-BGT) from the venom of the krait ( Bungarus multicinctus ). The purity of the isolated α-BGT was checked by electrofocusing and ion-exchange chromatography. Blockade of the binding of [ 3 H]ACh to the acetylcholine receptor in a membrane preparation of Torpedo electroplax was a convenient biochemical assay to identify the α-neurotoxin polypeptide. Iodination, accomplished by lactoperoxidase attached to Sepharose 4B, was simple and rapid, with a 60% recovery of [ 125 I]α-BGT. Biological activity of the α-BGT was determined by its toxicity to mice as well as by autoradiography of [ 125 I]α-BGT which proved its localization in the endplates of the mouse diaphragms.

An acetylcholine receptor-based optical biosensor was developed, which uses the evanescent wave to excite fluorescein isothiocyanate-labeled alpha-bungarotoxin (FITC-alpha-BGT), that is bound to a receptor protein immobilized on the surface of a quartz fiber. After excitation of the fluorophore just outside the waveguide boundary, the resultant fluorescence was trapped by and propagated back up the fiber. Pure nicotinic acetylcholine receptor (nAChR) protein, isolated from Torpedo electric organ, was immobilized noncovalently on quartz optic fibers and its density was quantitated by 125I-BGT binding. In the absence of nAChR, FITC-alpha-BGT alone bound to the quartz fiber. This nonspecific (i.e., nonreceptor) binding of FITC-alpha-BGT was totally eliminated by the addition of 0.1 mg/ml bovine serum albumin to the phosphate-buffered saline medium. This solution did not interfere with FITC-alpha-BGT binding to the nAChR that was immobilized on the fiber. Thus, only specific binding was observed under these conditions, resulting in a very high signal-to-noise ratio of greater than 99. Specific FITC-alpha-BGT binding to the nAChR protein on the optic fibers was inhibited by agonists (e.g., acetylcholine, nicotine, and carbamylcholine) and antagonists (e.g., pancuronium and d-tubocurarine) of the nAChR and was insensitive to high salt concentrations (e.g., 154 mM NaCl). The binding was most sensitive to the highly nAChR-specific alpha-BGT and alpha-cobratoxin. The optic-fiber sensor in its present form does not distinguish between receptor agonists or antagonist and cannot be regenerated for repeated use.(ABSTRACT TRUNCATED AT 250 WORDS)

This method involves the irreversible formation of a complex between 125I-labeled α-bungarotoxin and the acetylcholine receptor in either its membrane-bound or purified state. The separation of the labeled toxin-receptor complex from unreacted toxin is accomplished by chromatography on carboxymethylcellulose cation-exchange resin. The method described was developed to satisfy the following experimental requirements that could not be dealt with in their entirety by employing any of the published methods: (i) the complete recovery of reacted and unreacted species in relatively small volumes; (ii) an efficient and precise isolation of the specific and irreversible 125I-labeled α-bungarotoxin-receptor complex when the complexation reactions demand a large excess of unlabeled α-bungarotoxin for quenching (a 20-fold molar excess of unlabeled over labeled toxin); (iii) this isolation of the toxin-receptor complex allows one to determine the protein concentrations in the samples, a necessity in experiments covering a wide range of receptor concentrations; (iv) a consistent low blank for binding site concentrations ranging over two or three orders of magnitude; (v) simplicity and rapidity.

A thin-layer chromatographic method has been developed for the radiometric assay of minute quantities of acetylcholinesterase. It is simple, rapid, and allows the simultaneous assay and total recoveries of acetylcholine and acetate.