Paper
14 June 2004 Aequorin fusion proteins as bioluminescent tracers for competitive immunoassays
Mara Mirasoli, Elisa Michelini, Sapna K Deo, Emre Dikici, Aldo Roda, Sylvia Daunert
Author Affiliations +
Abstract
The use of bio- and chemiluminescence for the development of quantitative binding assays offers undoubted advantages over other detection systems, such as spectrophotometry, fluorescence, or radioactivity. Indeed, bio- and chemiluminescence detection provides similar, or even better, sensitivity and detectability than radioisotopes, while avoiding the problems of health hazards, waste disposal, and instability associated with the use of radioisotopes. Among bioluminescent labels, the calcium-activated photoprotein aequorin, originally isolated from Aequorea victoria and today available as a recombinant product, is characterized by very high detectability, down to attomole levels. It has been used as a bioluminescent label for developing a variety of highly sensitive immunoassays, using various analyte-aequorin conjugation strategies. When the analyte is a protein or a peptide, genetic engineering techniques can be used to produce protein fusions where the analyte is in-frame fused with aequorin, thus producing homogeneous one-to-one conjugation products, available in virtually unlimited amount. Various assays were developed using this strategy: a short review of the most interesting applications is presented, as well as the cloning, purification and initial characterization of an endothelin-1-aequorin conjugate suitable for developing a competitive immunoassay for endothelin-1, a potent vasoconstrictor peptide, involved in hypertension.
© (2004) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Mara Mirasoli, Elisa Michelini, Sapna K Deo, Emre Dikici, Aldo Roda, and Sylvia Daunert "Aequorin fusion proteins as bioluminescent tracers for competitive immunoassays", Proc. SPIE 5329, Genetically Engineered and Optical Probes for Biomedical Applications II, (14 June 2004); https://doi.org/10.1117/12.529194
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KEYWORDS
Proteins

Chemical analysis

Bioluminescence

Bacteria

Chemiluminescence

Luminescence

Radioisotopes

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