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Team:Carnegie Mellon/Our Sensor
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<h2> Sensor That Reports Endocrine Activating Molecules </h2> | <h2> Sensor That Reports Endocrine Activating Molecules </h2> | ||
<p><b> Background:</b> </p> | <p><b> Background:</b> </p> | ||
| - | <p> Currently a method to measure estrogenic compounds with eukaryotic cells already exists, using <i>S. cerevisiae</i> with an estrogen-binding domain of the human estrogen receptor alpha. However, this yeast estrogen-screening assay (YES assay) is slow in detecting estrogen. It usually takes several days to incubate the reporter cells with the samples in order to accumulate enough reporter protein and produce a measurable signal, which is not really suitable for large-scale sample screening <sup>[1]</sup>. </p> | + | <p> Currently a method to measure estrogenic compounds with eukaryotic cells already exists, using <i>S. cerevisiae</i> strain BJ3505 with an estrogen-binding domain of the human estrogen receptor alpha <sup>[1]</sup>. However, this yeast estrogen-screening assay (YES assay) is slow in detecting estrogen. It usually takes several days to incubate the reporter cells with the water samples in order to accumulate enough reporter protein and produce a measurable signal, which is not really suitable for large-scale sample screening <sup>[1]</sup>. </p> |
| - | <p>Another method is a bacterial beta-galactosidase assay to detect estrogenic compounds instead <sup>[1]</sup>. An intein, which is a splicing protein, sometimes called a protein intron, was used for this assay. When bound to its specific molecule, an intein will splice out and produce a functional protein. This method inserted the estrogen sensitive VMA intein into the constitutively expressed lacZ gene, | + | <p>Another method is a bacterial beta-galactosidase assay (or DIER assay) using <i> E. coli</i> strain DIER to detect estrogenic compounds instead <sup>[1]</sup>. An intein, which is a splicing protein, sometimes called a protein intron, was used for this assay. When bound to its specific molecule, an intein will splice out and produce a functional protein. This method inserted the estrogen sensitive VMA intein into two sites (between the Gly122 and Cys123 residues and Ala328 and Cys329 residues) in the essential region of the constitutively expressed lacZ gene <sup>[1]</sup>. In the presence of estrogenic compounds (such as 17-β estradiol), the intein would bind those, and splice out, to produce a functional LacZ protein<sup>[1]</sup>. A beta-galactosidase assay was utilized to produce a signal indicating the presence of estrogenic compounds<sup>[1]</sup>. However, this assay required a two hour incubation with 17-β estradiol for efficient splicing and was not very sensitive, having the same sensitivity as the YES assay <sup>[1]</sup>. This assay also and required a substrate. </p> |
<p/>A different method currently in use splits T7 RNA Polymerase (T7 RNAP) with a temperature sensitive intein, creating a temperature sensitive mutant <sup>[2]</sup>. This would result in transcription of the T7 promoter and terminator only at permissive temperatures. In order to construct a sensitive assay, a system to amplify the estrogen signal was required. We designed a system that inserted an estrogen sensitive intein inside T7 RNAP, a strong viral polymerase requiring no additional factors. In the presence of estrogen, functional T7 RNAP would be produced, and readily bind to the T7 promoter, resulting in signal amplification in the presence of estrogen. Production of functional T7 RNAP would be reported using a fluorescent protein. </p> | <p/>A different method currently in use splits T7 RNA Polymerase (T7 RNAP) with a temperature sensitive intein, creating a temperature sensitive mutant <sup>[2]</sup>. This would result in transcription of the T7 promoter and terminator only at permissive temperatures. In order to construct a sensitive assay, a system to amplify the estrogen signal was required. We designed a system that inserted an estrogen sensitive intein inside T7 RNAP, a strong viral polymerase requiring no additional factors. In the presence of estrogen, functional T7 RNAP would be produced, and readily bind to the T7 promoter, resulting in signal amplification in the presence of estrogen. Production of functional T7 RNAP would be reported using a fluorescent protein. </p> | ||
Revision as of 16:58, 30 September 2014
Project Title.
Our project description...
Our Sensor
Sensor That Reports Endocrine Activating Molecules
Background:
Currently a method to measure estrogenic compounds with eukaryotic cells already exists, using S. cerevisiae strain BJ3505 with an estrogen-binding domain of the human estrogen receptor alpha [1]. However, this yeast estrogen-screening assay (YES assay) is slow in detecting estrogen. It usually takes several days to incubate the reporter cells with the water samples in order to accumulate enough reporter protein and produce a measurable signal, which is not really suitable for large-scale sample screening [1].
Another method is a bacterial beta-galactosidase assay (or DIER assay) using E. coli strain DIER to detect estrogenic compounds instead [1]. An intein, which is a splicing protein, sometimes called a protein intron, was used for this assay. When bound to its specific molecule, an intein will splice out and produce a functional protein. This method inserted the estrogen sensitive VMA intein into two sites (between the Gly122 and Cys123 residues and Ala328 and Cys329 residues) in the essential region of the constitutively expressed lacZ gene [1]. In the presence of estrogenic compounds (such as 17-β estradiol), the intein would bind those, and splice out, to produce a functional LacZ protein[1]. A beta-galactosidase assay was utilized to produce a signal indicating the presence of estrogenic compounds[1]. However, this assay required a two hour incubation with 17-β estradiol for efficient splicing and was not very sensitive, having the same sensitivity as the YES assay [1]. This assay also and required a substrate.
A different method currently in use splits T7 RNA Polymerase (T7 RNAP) with a temperature sensitive intein, creating a temperature sensitive mutant [2]. This would result in transcription of the T7 promoter and terminator only at permissive temperatures. In order to construct a sensitive assay, a system to amplify the estrogen signal was required. We designed a system that inserted an estrogen sensitive intein inside T7 RNAP, a strong viral polymerase requiring no additional factors. In the presence of estrogen, functional T7 RNAP would be produced, and readily bind to the T7 promoter, resulting in signal amplification in the presence of estrogen. Production of functional T7 RNAP would be reported using a fluorescent protein.References:
[1] Liang R, Zhou J, Liu J; “Construction of Bacterial Assay for Estrogen Detection Based on Estrogen-Sensitive Intein,” Applied and Environmental Microbiology, Vol. 77, No. 7; September 30, 2010.
[2] Liang R, Liu X, Liu J, Ren Q, Liang P, Lin Z, Xie X; “A T7-expression system under temperature control could create temperature-sensitive phenotype of target gene in Escherichia coli,” Journal of Microbiological Methods 68 (2007) 497–506.
