Difference between revisions of "Part:BBa K4339002"

Revision as of 11:20, 12 October 2022

MaSp1_K3264003mod_CT E. australis

A major ampullate spidroin 1 (MaSp1) based protein consisting of the Great Bay 2019 part BBa_K3264003 fused to a C-terminal domain from the African nursery web spider Euprosthenops australis. Due to the highly repetitive nature of spidroin proteins, the DNA coding sequences are also highly repetitive. Unfortunately we were unable to submit the original Great Bay sequence for synthesis, and therefore K3264003 had to be modified to allow for synthesis.

Usage and Biology

Sequence and Features

K3264002mod original sequence originates from the common orb-weaving spider Araneus ventricosus [1]. This sequence is composed of 2 repeated poly-alanine and poly-glycine regions.

CT domain sequence originates from the African nursery web spider Euprosthenops australis [2].

All MaSp parts (K4339002 - K4339010) can be categorised as either MaSp1 or MaSp2 proteins, which form the major components of spider dragline silk. Both protein types comprise of repeated poly-alanine and glycine rich regions. Hydrophobic interactions between poly-alanine regions and hydrophilic interactions between glycine-rich regions confer the strength and elasticity of dragline silk respectively [3]. The non-repetitive N- and C-terminal domains of these proteins are suggested to contribute towards protein solubility and self-assembly in the abdominal glands of spiders, where proteins are exposed to a pH gradient as they are drawn through an abdominal duct [4]. Following the protocol for spontaneous fibre assembly from MaSps outlined in [2], which occurs in the absence of a pH gradient, the N-terminal domains, which only contribute to fibre assembly via interactions with such a gradient, would be non-functional, so was removed from all MaSp constructs.

Results reported in [2] show the number of repeated poly-alanine and glycine rich regions controls fibre length, ranging from millimetre to metre scale. Results further show that removing the C-terminal domain causes formation of an amorphous aggregate of short fibres. Thus, MaSp constructs were designed containing various numbers of repeated regions, with and without C-terminal domains, with an aim to generate fibres of a range of structures, to explore the resultant differences in their mechanical properties.

In silico studies predict that MaSp1 and MaSp2 proteins have distinctly different mechanical behaviour, with the overall mechanical properties of a silk fibre being partially dependent on the ratio of the two protein types [5]. MaSp1 is predicted to contribute more greatly to elasticity of a silk fibre, whilst MaSp2 is predicted to contribute more significantly to its Young's modulus (a measure of a material's resistance to deformation). Therefore, to explore the range of possible mechanical properties of recombinant spider silk, both MaSp1 and MaSp2 parts were designed, with an aim to express and purify both protein types, before mixing them in a variety of ratios and triggering their spontaneous self-assembly into fibres.

All MaSp parts were designed to be integrated into devices, fused with a His tag (6 x Histidine) and solubility tag TrxA (BBa_K3619001) with a thrombin cleavage site between them. TrxA is a small, highly soluble protein which, when fused with a protein of interest, can act as a molecular chaperon, guiding protein folding and preventing inclusion body formation [6], as well as increasing the solubility of the fusion partner. As per the methodology set out in [2], TrxA-fused MaSp proteins were designed to be soluble in the cytosol of E. coli when expressed, so they could be extracted in the soluble portion cell lysate. MaSps would be purified from the lysate using a Nickel-NTA column (which binds his-tagged proteins). Thrombin would then be added to the elution from the column to cleave off the TrxA tag, causing MaSp proteins to precipitate out of solution and spontaneously self-assemble into fibres.

K3264003mod_CTEa was successfully inserted into a holding plasmid and sequence verified, with a repeated region of K3264003mod missing. A His-tagged device containing this part was built in a medium-copy plasmid vector under the control of the inducible T7 promoter and sequence verified. It was then transformed into Rosetta DE3 E. coli, but expression was not able to be confirmed via Western blotting. A TrxA+His-tagged device containing this part was built similarly but sequence fidelity was poor.

References

[1] - Andersson, Marlene, et al. Biomimetic Spinning of Artificial Spider Silk from a Chimeric Minispidroin. Nature Chemical Biology. 2017;13(3): 262–264. doi: https://doi.org/10.1038/nchembio.226

[2] - Stark M et al. Macroscopic fibers self-assembled from recombinant miniature spider silk proteins. 2007;8(5): 1695–1701. doi: https://doi.org/10.1021/bm070049y.

[3] - Xia X et al. Native-sized recombinant spider silk protein produced in metabolically engineered Escherichia coli results in a strong fiber. Proc Natl Acad Sci USA. 2010;107(32): 14059-63. doi: https://doi.org/10.1073/pnas.1003366107

[4] - Gaines W et al. Recombinant Dragline Silk-Like Proteins-Expression and Purification. AATCC Rev. 2011;11(2): 75-79. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729042/ [Accessed 12/10/22]

[5] - Brooks A et al. Distinct contributions of model MaSp1 and MaSp2 like peptides to the mechanical properties of synthetic major ampullate silk fibers as revealed in silico. Nanotechnol Sci Appl. 2008;1: 9-16. doi: https://doi.org/10.2147/nsa.s3961

[6] - LaVallie E et al. Thioredoxin as a fusion partner for production of soluble recombinant proteins in Escherichia coli. Methods in Enzymology. 2000;326: 322-340. doi: https://doi.org/10.1016/S0076-6879(00)26063-1