DNA Origami Assembly for the Tar Chemoreceptor: Difference between revisions
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==Attachment to DNA== | ==Attachment to DNA== | ||
The protein receptor dimer is <scene name='80/800127/ | The protein receptor dimer is <scene name='80/800127/Zoomed_in_connection_color/1'>attached to the tetrahedron</scene> using NTA-functionalized DNA. This means that the DNA has an NTA, or nitrilotriaceticacid, is able to coordinate with nickel ions, shown in green, which is also able to coordinate with histidines. The Tar chemoreceptor has six histidines added to the N-terminus of the protein ''in vitro'', which should be able to coordinate with the nickel ion as well, creating a coordination complex. | ||
</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
<references/> | <references/> |
Revision as of 23:34, 1 November 2018
DNA Origami as an Assembly Method for Tar ChemoreceptorDNA Origami as an Assembly Method for Tar Chemoreceptor
This project centers around the idea of using DNA origami to assemble the Tar chemoreceptor. This assembly method would provide novel opportunities to investigate how this receptor works previously untestable using other assembly methods You may include any references to papers as in: the use of JSmol in Proteopedia [1] Introduction to ChemotaxisChemotaxis is the process by which bacteria sense chemicals in their environment. This is done through the use of chemoreceptors to sense a chemical gradient that they can follow towards higher concentrations of food or away from higher concentrations of poisons or other unfavorable conditions. The Tar chemoreceptor is involved with the sensing of aspartate, a common amino acid, by binding aspartate in the extracellular portion of the protein and then propagates a signal down the receptor to activate a pathway to alter movement. [Add picture of chemoreceptor here? Are there any that are open source?] Possible Applications of ChemotaxisUnderstanding how signals are propagated in chemotaxis would be incredibly helpful in the fight against antibiotic resistance. Being able to control bacterial movement could allow a treatment to be engineered to move bacteria either towards antibiotics, therefore reducing the necessary dosage, or away from food or nutrients, effectively starving the bacteria. In addition, being able to use bacteria as carriers for drugs could also be a novel drug delivery technique. DNA OrigamiThis project involves using a DNA tetrahedron as a scaffold for the Tar chemoreceptor complex in vitro. In this model, receptor dimers are attached at three vertices of the DNA tetrahedron to make the native structure seen in vivo. At the other end of the receptor, two proteins are shown: CheA, a kinase, shown in blue, and CheW, a coupling protein, shown in cyan. Attachment to DNAThe protein receptor dimer is using NTA-functionalized DNA. This means that the DNA has an NTA, or nitrilotriaceticacid, is able to coordinate with nickel ions, shown in green, which is also able to coordinate with histidines. The Tar chemoreceptor has six histidines added to the N-terminus of the protein in vitro, which should be able to coordinate with the nickel ion as well, creating a coordination complex.
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ReferencesReferences
- ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024