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Team:USTC/Tool
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== Results == | == Results == | ||
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| + | In the electrophoretogram, only the combination of primer 5 & plasmid 5, primer 6 & plasmid 6, primer 7 & plasmid 7 lead to PCR result. | ||
| + | [[Image:tool_result.png|100px|right|frame]] | ||
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== Application == | == Application == | ||
Revision as of 10:59, 1 October 2009
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Team:USTC/Tool
Contents |
Introduction
Problem 1: How to distinguish the different biobricks in a biobrick-pool in experiment?
To take a DNA sequencing?---it's costly and time-consuming.
We are faced with such a problem to determine the final outputs of E.ADEM (E.coli Automatic Directed Evolution Machine)[1]. An inspiration comes from the supermarket checkout system where thousands of commodities are tagged by barcodes. This universal commercial ID both shortens the check-out time and adds the accuracy. By comparing our problem with this system, what we need to do can be concluded as to design barcodes for biobricks, BioBrick-Barcode, as we call it.
Problem 2: Where is the scanner?
PCR (Polymerase Chain Reaction)[http://en.wikipedia.org/wiki/PCR], which is so conveniently conducted, can serve as the scanner while the primers it needs are the analogue of barcode sequences.
Solution: To check the final outputs in the system of E.ADEM (E.coli Automatic Directed Evolution Machine), we need to design a set of DNA oligo-sequences primers as the barcodes to go through the scanner of PCR and help determining the final evolutionary products.
Design
A set of barcodes under a certain kind of barcode reader has to satisfy its conditions in order to be picked out respectively. For BioBrick-Barcodes, the oligo-sequences must meet several conditions as we considered:
1. Since the BioBrick-Barcodes function as PCR primers, they must satisfy the basic conditions as high-quality primers:
a. Each primer should be 20-30 nucleotides in length; b. Contain approximately equal numbers of 4 bases, with a balanced distribution of G&C residues; c. Hold a low propensity to form stable secondary structures; d. Forward and reverse primers can work properly together;
2. As a set of barcodes, each of the primers should be perceivably different in order to be identified by the scanner:
a. Any one of the primer cannot lead to the PCR of other DNA sequences(a plasmid with a certain target sequence.) b. All of the primers should be specific for the target sequence without combining with other sites.
Software
Primer3[http://primer3.sourceforge.net/releases.php] is an open-source primer-design software, and we modified its C codes in parts to design the BioBrick-Barcodes. Since Primer3 is mainly used to pick primers from a DNA template while the BioBrick-Barcodes are supposed to be randomly produced, and a set of BioBrick-Barcodes should be diverse to avoid overlapping PCR, we changed three functions and structure of Primers.
1. Add a function to randomly produce the DNA oligo-sequences which replaced the previous function used to pick
segments from the template.
2. Modified the structure used to store information of each primer.
3. Use the Libray_Mispriming to choose diverse primers.
Experiment
We design a set of ten diverse primers by using the modified software. Apparently, we need to conduct experiments to test its feasibility.
1.Synthesize the DNA oligo-sequence;
2.Construct plasmids;
3.Conduct a 10*10 cross experiment: Each primer reacts with all the plasmids;
Expectation: only complementary couple leads to PCR results.
Results
In the electrophoretogram, only the combination of primer 5 & plasmid 5, primer 6 & plasmid 6, primer 7 & plasmid 7 lead to PCR result.
