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Team:MIT/Motivation
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| - | <b>Total size of circuit: ~17, | + | <b>Total size of circuit: ~17,600 bp</b> |
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| - | <b>Total size of circuit: ~3, | + | <b>Total size of circuit: ~3,000 bp</b> |
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Revision as of 01:10, 3 October 2012
Motivation
Let's look at a potential synthetic biology application: detecting cancer state in mammalian cells. We'll compare traditional, promoter-based synbio logic with a novel strategy from the field of DNA computing: strand displacement.
Parts required (see below for explanation):
- 5 input sensor modules
- 5 processor modules (one for each input)
- 1 actuation module
Promoter-based logic
|
Strand displacement-based logic
|
|
Promoter-protein pairs required: 11 (one for each module)
Max achieved in literature: 6 |
Strands of nucleic acid required: 80 |
| Size of each promoter-protein pair: ~1,600 bp | Length of each strand: ~40 bp |
| Total size of circuit: ~17,600 bp | Total size of circuit: ~3,000 bp |
Currently, the traditional method of synthetic biology uses proteins as on/off signals for cell based computing. As evident in the example above, the potential of these circuits is fundamentally limited by the number of proteins that can be orthogonally and simultaneously expressed.
Imagine a circuit that senses for potential cancer cells and then produces a fluorescent protein that allows the cells to be easily identified by a doctor or surgeon. What would this require?
The first step, a cancer cell sensor, can be achieved by creating an mRNA sensor. The state of the art circuit with this function, (1 Multi-Input RNAi-Based Logic Circuit for Identification of Specific Cancer Cells. Xie et al. Science 2011) requires at least five composite parts for sensing high and low mRNA concentrations. The next part would need to process information from these five separate inputs, invert some of it, and send a signal to up regulate fluorescent protein production. This would require another set of promoters for each sensed mRNA and a repression system to produce the correct logic. The last step would be the induced expression of the signal protein; another unique promoter and protein pairing.
This hypothetical circuit requires at least eleven unique promoters and proteins to function. At 1600 nucelotides per composite part, that means inserting 17,600 new bases into the cellular DNA. As shown in the graph above, the current maximum number of promoters in a cellular circuit is six.
Clearly, a novel method of information processing is needed if we want to create complex circuits in vivo. For inspiration, we turned to "Scaling up digital circuit computation with DNA strand displacement cascades." Qian, L., Winfree, E. Science 2011. That research shows that it is possible to use the method of DNA strand displacement for complex circuits in vitro. The team built a circuit which calculated square roots with inputs of different short DNA strands representing binary numbers. The same hypothetical cancer sensing and highlighting circuit, designed using the strand displacement motif, requires only 3200 nucleotides of coding, creating over eighty strands which are roughly 40 bases in length.
Integrating this into a ceullar system is non-trivial, but possible.
