Team:Brown-Stanford/FRETSensor/Introduction

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== '''Introduction''' ==
== '''Introduction''' ==
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Biosensor is a novel mechanism of FRET reporting using engineered parts of the bacterial cellulosome in the form of cohesin-dockerin pairs. We will create a two cohesin complex to bring together constitutive RFP and CFP reporters bound to dockerins. The cohesin complex will cause FRET reporting that should be faster than traditional methods which require maturation of GFP-based reporters.  
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Monitoring various aspects of the Martian environment with machinery requires a variety  probes and possibly a large amount of energy for continual detection. A more cost-effective and long-term solution to the problem of sensing changes in the environment is to use a variety of living microbes that are genetically programmed to respond to certain specific stimuli. Microbial biosensors work in essentially the same manner as a conventional sensor: the cell is equipped with a physical transducer that will induce a detectable signal once stimulated. However, the major advantage of a microbial sensor over inorganic sensors in the space environment is its ability to be mass produced from very little external input.
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Optical microbial biosensors come in a variety of flavors: fluorescent, bioluminescent, and colorimetric. In vivo fluorescent biosensors make use of an inducible promoter fused to a reporter gene encoding a fluorescent protein such that the protein is produced in proportion to the quantity of analyte detected. Other biosensors may also be binary and detect presence or absence. [...]
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One drawback of a protein reporter is its lower sensitivity and longer response time in comparison to bioluminescent-based reporters. On the other hand, fluorescent proteins are highly stable once formed and can be analyzed days after the detection event. These two features make reporters systems using GFP and its variants amenable to detection of trace environmental elements such as radiation dosimetry, micronutrients, toxins, other organisms, etc. Because of the longer response time, one application protein-based reporters is not suited for is a warning system. In a review of many GFP variants, the t0.5 for maturation at 37°C varied from 15 minutes to over four hours [2].
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Our team wanted to be able to detect rapid changes in environment or condition of the cell using fluorescent proteins and increase the scope of microbial biosensors to that of early warning systems.Therefore, we decided to make novel use of an existing mechanism, FRET, that can make use of fluorescent proteins to image fast changes in cell state.
[[File:Brown-Stanford CohesinDockerin.png|center|400px]]
[[File:Brown-Stanford CohesinDockerin.png|center|400px]]
{{:Team:Brown-Stanford/Templates/Foot}}
{{:Team:Brown-Stanford/Templates/Foot}}

Revision as of 15:31, 24 September 2011

Brown-Stanford
iGEM

Introduction

Monitoring various aspects of the Martian environment with machinery requires a variety probes and possibly a large amount of energy for continual detection. A more cost-effective and long-term solution to the problem of sensing changes in the environment is to use a variety of living microbes that are genetically programmed to respond to certain specific stimuli. Microbial biosensors work in essentially the same manner as a conventional sensor: the cell is equipped with a physical transducer that will induce a detectable signal once stimulated. However, the major advantage of a microbial sensor over inorganic sensors in the space environment is its ability to be mass produced from very little external input.

Optical microbial biosensors come in a variety of flavors: fluorescent, bioluminescent, and colorimetric. In vivo fluorescent biosensors make use of an inducible promoter fused to a reporter gene encoding a fluorescent protein such that the protein is produced in proportion to the quantity of analyte detected. Other biosensors may also be binary and detect presence or absence. [...]

One drawback of a protein reporter is its lower sensitivity and longer response time in comparison to bioluminescent-based reporters. On the other hand, fluorescent proteins are highly stable once formed and can be analyzed days after the detection event. These two features make reporters systems using GFP and its variants amenable to detection of trace environmental elements such as radiation dosimetry, micronutrients, toxins, other organisms, etc. Because of the longer response time, one application protein-based reporters is not suited for is a warning system. In a review of many GFP variants, the t0.5 for maturation at 37°C varied from 15 minutes to over four hours [2].

Our team wanted to be able to detect rapid changes in environment or condition of the cell using fluorescent proteins and increase the scope of microbial biosensors to that of early warning systems.Therefore, we decided to make novel use of an existing mechanism, FRET, that can make use of fluorescent proteins to image fast changes in cell state.

Brown-Stanford CohesinDockerin.png

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