Literature DB >> 12123657

Bioluminescence immunoassay for cortisol using recombinant aequorin as a label.

Mara Mirasoli1, Sapna K Deo, Jennifer C Lewis, Aldo Roda, Sylvia Daunert.   

Abstract

The analysis of hormones in saliva is a powerful tool in the assessment of a patient's endocrine function, since it allows multiple noninvasive samplings. Since salivary levels of most hormones are 10 to 50 times lower than plasma levels, accurate and highly sensitive assays are needed for saliva measurements. Herein, we describe the development of a solid-phase competitive immunoassay for cortisol in saliva, in which a mutant of the photoprotein aequorin has been used as a label. We have chemically conjugated cortisol to aequorin at different molar ratios. The various cortisol-aequorin conjugates were characterized in terms of bioluminescent activity and affinity for the anti-cortisol antibody. The conjugate that gave the best analytical performance was used for the development of the immunoassay and the analysis of cortisol in saliva samples. The conjugates were stable for at least 6 months when stored at 4 degrees C. The method fulfilled all the standard requirements of precision and accuracy. The optimized immunoassay gave a detection limit of 300 fmol/tube, corresponding to 3 nmol/L, with a linear dynamic range of 10-1000 nmol/L. Therefore, cortisol can be detected down to 0.1 ng in 100 microl of saliva sample using this assay, without any sample pretreatment. This detection limit is almost one order of magnitude lower than the physiological levels of salivary cortisol, which are reported to be 10-25 nmol/L. This allows the quantification of salivary cortisol to be performed in the linear range of the calibration curve, which is most reliable for quantification purposes.

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Keywords:  Non-programmatic

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Year:  2002        PMID: 12123657     DOI: 10.1006/abio.2002.5695

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  7 in total

1.  Immunosensor with fluid control mechanism for salivary cortisol analysis.

Authors:  Masaki Yamaguchi; Yohei Matsuda; Shohei Sasaki; Makoto Sasaki; Yoshihiro Kadoma; Yoshikatsu Imai; Daisuke Niwa; Vivek Shetty
Journal:  Biosens Bioelectron       Date:  2012-08-16       Impact factor: 10.618

2.  Cyclic AMP receptor protein-aequorin molecular switch for cyclic AMP.

Authors:  Daniel Scott; Krystal Teasley Hamorsky; C Mark Ensor; Kimberly W Anderson; Sylvia Daunert
Journal:  Bioconjug Chem       Date:  2011-02-17       Impact factor: 4.774

3.  Molecular evolution of a steroid hydroxylating cytochrome P450 using a versatile steroid detection system for screening.

Authors:  Cornelia Virus; Rita Bernhardt
Journal:  Lipids       Date:  2008-10-01       Impact factor: 1.880

4.  Detection of cortisol in saliva with a flow-filtered, portable surface plasmon resonance biosensor system.

Authors:  Richard C Stevens; Scott D Soelberg; Steve Near; Clement E Furlong
Journal:  Anal Chem       Date:  2008-07-26       Impact factor: 6.986

Review 5.  Ca2+-regulated photoproteins: effective immunoassay reporters.

Authors:  Ludmila A Frank
Journal:  Sensors (Basel)       Date:  2010-12-10       Impact factor: 3.576

6.  Automated-immunosensor with centrifugal fluid valves for salivary cortisol measurement.

Authors:  Masaki Yamaguchi; Hiroki Katagata; Yuki Tezuka; Daisuke Niwa; Vivek Shetty
Journal:  Sens Biosensing Res       Date:  2014-07-09

7.  Red-Shifted Aequorin Variants Incorporating Non-Canonical Amino Acids: Applications in In Vivo Imaging.

Authors:  Kristen M Grinstead; Laura Rowe; Charles M Ensor; Smita Joel; Pirouz Daftarian; Emre Dikici; Jean-Marc Zingg; Sylvia Daunert
Journal:  PLoS One       Date:  2016-07-01       Impact factor: 3.240

  7 in total

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