Fluorescence Assay for Polymerase Arrival Rates

To engineer complex synthetic biological systems will require modulardesign, assembly, and characterization strategies. The RNApolymerase arrival rate (PAR) is defined to be the rate that RNApolymerases arrive at a specified location on the DNA. Designing andcharacterizing biological modules in term...

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Main Author: Che, Austin
Language:en_US
Published: 2005
Subjects:
AI
Online Access:http://hdl.handle.net/1721.1/30406
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author Che, Austin
author_facet Che, Austin
author_sort Che, Austin
collection MIT
description To engineer complex synthetic biological systems will require modulardesign, assembly, and characterization strategies. The RNApolymerase arrival rate (PAR) is defined to be the rate that RNApolymerases arrive at a specified location on the DNA. Designing andcharacterizing biological modules in terms of RNA polymerase arrivalrates provides for many advantages in the construction and modeling ofbiological systems.PARMESAN is an in vitro method for measuring polymerase arrival ratesusing pyrrolo-dC, a fluorescent DNA base that can substitute forcytosine. Pyrrolo-dC shows a detectable fluorescence difference whenin single-stranded versus double-stranded DNA. During transcription,RNA polymerase separates the two strands of DNA, leading to a changein the fluorescence of pyrrolo-dC. By incorporating pyrrolo-dC atspecific locations in the DNA, fluorescence changes can be taken as adirect measurement of the polymerase arrival rate.
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spelling mit-1721.1/304062019-04-09T16:26:46Z Fluorescence Assay for Polymerase Arrival Rates Che, Austin AI To engineer complex synthetic biological systems will require modulardesign, assembly, and characterization strategies. The RNApolymerase arrival rate (PAR) is defined to be the rate that RNApolymerases arrive at a specified location on the DNA. Designing andcharacterizing biological modules in terms of RNA polymerase arrivalrates provides for many advantages in the construction and modeling ofbiological systems.PARMESAN is an in vitro method for measuring polymerase arrival ratesusing pyrrolo-dC, a fluorescent DNA base that can substitute forcytosine. Pyrrolo-dC shows a detectable fluorescence difference whenin single-stranded versus double-stranded DNA. During transcription,RNA polymerase separates the two strands of DNA, leading to a changein the fluorescence of pyrrolo-dC. By incorporating pyrrolo-dC atspecific locations in the DNA, fluorescence changes can be taken as adirect measurement of the polymerase arrival rate. 2005-12-19T22:50:24Z 2005-12-19T22:50:24Z 2003-08-31 MIT-CSAIL-TR-2003-017 AITR-2003-017 http://hdl.handle.net/1721.1/30406 en_US Massachusetts Institute of Technology Computer Science and Artificial Intelligence Laboratory 112 p. 113486485 bytes 7023595 bytes application/postscript application/pdf application/postscript application/pdf
spellingShingle AI
Che, Austin
Fluorescence Assay for Polymerase Arrival Rates
title Fluorescence Assay for Polymerase Arrival Rates
title_full Fluorescence Assay for Polymerase Arrival Rates
title_fullStr Fluorescence Assay for Polymerase Arrival Rates
title_full_unstemmed Fluorescence Assay for Polymerase Arrival Rates
title_short Fluorescence Assay for Polymerase Arrival Rates
title_sort fluorescence assay for polymerase arrival rates
topic AI
url http://hdl.handle.net/1721.1/30406
work_keys_str_mv AT cheaustin fluorescenceassayforpolymerasearrivalrates