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Synthetic Biology: What's Hindering Us?

Efforts in synthetic biology have been primarily focused on the creation and perfection of biological modules and systems in order to achieve specific functions. Since first demonstrated by the bacterial toggle switch and the Repressilator in 2000, synthetic biologists now possess the ability to engineer and manipulate genetic circuits, metabolic pathways, and even entire genomes.

In genetic engineering, chemicals are frequently employed as signals to control molecular and cellular behavior. However, because chemicals deliver information only by diffusion, chemical signals are seriously limited by the short-range interactions. Another serious issue regarding chemical signals is the complexity of the process in fully eradicating them, making it difficult for the system to reset. Additionally, the cytotoxicity, high cost, and narrow dynamic range of chemicals urge synthetic biologists to find more spatiotemporally specific and environmental friendly alternatives.

comparison of Chemical and light

Figure 1. Comparison of chemical signal and light signal

Optogenetics: Inspiring Synthetic Biology

Literally, optogenetics refers to the genetic strategies which employ light as the input signal in the place of chemical signals. During the last decade, optogenetics has made significant impact on life sciences and other practices[1]. It has evolved rapidly, with light-switchable promoters[2], light-induced protein-protein interaction[3], light-activated ion channelsand[4] eventually, light-controlled animal behavior, and so on. The spatiotemporal specificity of light signals allows for precise manipulation and long range interaction without physical contact. Besides its incredible range of functions, light resources are also cheaper, more sustainable, and environmentally friendly. These properties together make optogenetic tools attractive for synthetic biologists.

[Fig 2.]

Figure 2. Evolution of Optogenetics[6]

Reference

  • 1. Miesenbock, G. (2011) Optogenetic control of cells and circuits. Annu. Rev. Cell. Dev. Biol., 27: 731: 758
  • 2. Shimizu-Sato, S., Huq, E., et al. (2002) A light-switchable gene promoter system. Nat. Biotechnol., 20(10): 1041: 1044
  • 3. Levskaya, A., Weiner, O.D., et al. (2009) Spatiotemporal control of cell signalling using a light-switchable protein interaction. Nature, 461(7266): 997: 1001.
  • 4. Zemelman, B.V., Lee, G.A., et al. (2002) Selective photostimulation of genetically chARGed neurons. Neuron, 33(1): 15: 22
  • 5. Ohlendorf, R., Vidavski, R.R., et al. (2012) From dusk till dawn: one-plasmid systems for light-regulated gene expression. J. Mol. Biol. 416(4): 534: 542
  • 6. http://www.stanford.edu/group/dlab/optogenetics/
  • Totop Totop

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