Team:Kent/Description
Project Description
Overview
Our project aims to produce self-assembling conductive nanowire by harnessing an endogenous amyloid export system in E.coli. This could be used to replace current nanowire technology that relies on chemical synthesis. Amyloid is a unique material exhibiting high mechanical strength, comparable to that of steel[1] , and high thermal stability.
csgA signal sequence
The bipartite csgA signal sequence is a chain of amino acids that targets our protein to the Sec protein export pathway followed by endogenous curli export pathway [2] [3] via interaction with the chaperone csgG. This allows our protein to be exported from the E.coli cell and form a high concentration of monomers in the extracellular medium.
Sup35-NM
The protein that we have chosen to use is Sup35-NM, derived from the Sup35 protein found in yeast. Amyloid formation occurs due to stacking interactions of the N domain [4] [5] and each individual Sup35-NM is sufficiently small and closely stacked to allow the flow of electrons. The amyloid has desirable characteristics for nanostructures, such as heat resistance at both high and low temperatures ranging from 98℃ to -80℃ [6] , as well as high mechanical and chemical stability.
We have improved a previously designed BioBrick (Part:BBa_K401001) from the Valencia 2010 iGEM team that encoded the Sup35 protein from Saccharomyces cerevisiae. The previously designed BioBrick contained two illegal cut sites for Pstl and one for Bsal.rc within the coding region that reduce compatibility for digestion and modification of the part. Our improved BioBrick has used genome optimisation in order to remove these cut sites, producing a part compatible with the iGEM part submission standards. Validation of this part used a diagnostic Congo Red plate that demonstrated the presence of amyloid by formation of red colonies.
Cytochrome b562
To make our amyloid conductive we have the electron carrier cytochrome b562 bound to Sup35-NM as a fusion protein. Our protein follows the Sec export pathway before entering the curli export system. This means that our protein will be exported in an unfolded conformation. Type b cytochromes bind haem non-covalently and bind to the central iron via to the two ligands Methionine-7 and Histidine-106 [7] , thus allowing exogenous addition of haem. To facilitate the flow of electrons to consecutive cytochromes, the haem groups must be within 20Å of each other. Due to the small size and close interaction of Sup35-NM monomers, we predict that the distance between haem groups will range from 4Å to 15Å.
Similar work has been carried out harnessing amyloid produced in vitro by a derivative of Sup35-NM with engineered cysteine residues to bind Nanogold particles. This work found that the distance between the Nanogold particles was too large to be conductive and thus a bridging technique was required to reduce of the 3-5nm gap, consequently forcing the diameter of the amyloid to be increased from 9-11nm to 80-200nm [6] .
Amyloid
In the past amyloid has been surrounded by a negative connotation due to association with diseases such as Alzheimer’s, type II diabetes, and Parkinson’s. In recent years however, functional amyloid has been discovered. Organisms are able to harness functional amyloid in a beneficial manner in order to carry out biological functions, for example biofilm formation in E.coli, regulation of the STOP codon in S.cerevisiae, and coordinating the chemistry of melanin biosynthesis in mammals [8] . Amyloid fibres possess desirable properties as a material to work with because they show mechanical strength comparable to steel and stiffness comparable to silk [1] , thus making them easy to manipulate but difficult to break down.
Future perspectives
In the future we believe that our product could be used either to produce nanowires that can be purified from the E.coli cells or could be modified into a fuel cell that produces electricity and nanowire.
The amyloid nanowire produced from our BioBrick in the VS45 strain of E.coli produces a high concentration of amyloid nanowires that are free from the cell and could be purified for use in nano-circuitry. Some of the advantages of using amyloid nanowires include high mechanical strength, thermal, and chemical stability, as well as being environmentally friendly by greatly reducing carbon emissions from production. Complex circuit diagrams can be produces from Sup35-NM amyloid fibres using techniques such as lithography, growth in flows or magnetic field gradients, alignment by electrical fields, active patterning with optical tweezers, dielectrophoresis and 3D patterning using hydrogels or microfluidic channels [1] . This will allow the generation of miniature circuit diagrams that could pave the way to advancements in nanoscale communications. The high thermal stability is a favourable characteristic because circuit boards can run up to a temperature of 70°C and silver nanowires with a diameter of 5nm disintegrate into individual nanoclusters at a temperature of 27°C [9] .
Another branch that this project could take would be to engineer a bacterial cell that transports some electrons from the electron transport chain (ETC) into the amyloid-nanowires. This would need to be done using a strain other than VS45 so that the amyloid fibres would attach to the outer surface of the bacterial cell. As a consequence this would create a product that generates its own electricity and transports it along nanowires produced by the same cell; resulting in a living, self-assembling, energy producing circuit board that could be used in a range of consumer products.
References
[1] Smith, J., Knowles, T., Dobson, C., MacPhee, C. and Welland, M. (2006). Characterization of the nanoscale properties of individual amyloid fibrils. Proceedings of the National Academy of Sciences, 103(43), pp.15806-15811.
[2] Sivanathan, V. and Hochschild, A. (2012). Generating extracellular amyloid aggregates using E. coli cells. Genes & Development, 26(23), pp.2659-2667
[3] Sivanathan, V. and Hochschild, A. (2013). A bacterial export system for generating extracellular amyloid aggregates. Nat Protoc, 8(7), pp.1381-1390.
[4] Frederick, K., Debelouchina, G., Kayatekin, C., Dorminy, T., Jacavone, A., Griffin, R. and Lindquist, S. (2014). Distinct Prion Strains Are Defined by Amyloid Core Structure and Chaperone Binding Site Dynamics. Chemistry & Biology, 21(2), pp.295-305.
[5] Glover, J., Kowal, A., Schirmer, E., Patino, M., Liu, J. and Lindquist, S. (1997). Self-Seeded Fibers Formed by Sup35, the Protein Determinant of [PSI+], a Heritable Prion-like Factor of S. cerevisiae. Cell, 89(5), pp.811-819.
[6] Scheibel, T., Parthasarathy, R., Sawicki, G., Lin, X., Jaeger, H. and Lindquist, S. (2003). Conducting nanowires built by controlled self-assembly of amyloid fibers and selective metal deposition. Proceedings of the National Academy of Sciences, 100(8), pp.4527-4532.
[7] Xavier, A., Czerwinski, E., Bethge, P. and Mathews, F. (1978). Identification of the haem ligands of cytochrome b562 by X-ray and NMR methods. Nature, 275(5677), pp.245-247.
[8] Fowler, D., Koulov, A., Balch, W. and Kelly, J. (2007). Functional amyloid – from bacteria to humans. Trends in Biochemical Sciences, 32(5), pp.217-224.
[9] Gordon, E., Karabulin, A., Matyushenko, V. and Khodos, I. (2015). Experimental Study of Thermal Stability of Thin Nanowires. J. Phys. Chem. A, 119(11), pp.2490-2501.
