Revision as of 20:42, 23 July 2015

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HONEYBEE SILK PROJECT

Goals

The goal of this project is to recombinantly express honeybee silk proteins, with the intention of creating synthetic honeybee silk fibers. We hope to develop protocols to efficiently produce the raw protein, process the protein into various materials, and characterize these materials. Furthermore, by conjugating the honeybee protein with other proteins, we aim to create honeybee silk materials with a wide array of properties and functionalities.

Achievements

As of 5/16 we are well on our way to establishing a strong foundation for this project. We have cloned some honeybee sequences into biobrick approved format, and are on our way to expressing our first batch of honeybee silk protein. (For detailed achievements see below)

Cloning

We have successfully cloned and sequence verified two honeybee silk constructs into the igem psb1c3 plasmid backbone, in the correct biobrick format. A comprehensive list of our honeybee parts can be found here

• The first sequence is just the honeybee silk protein #3 in the psb1c3 backbone. The annotated sequence, along with further details on how we designed and cloned this biobrick can be found here. [http://parts.igem.org/Part:BBa_K1763000 BBa_K1763000]
• The second sequence is the same silk coding sequence, but with regulatory elements upstream for protein expression, including [http://parts.igem.org/Part:BBa_R0010 BBa_R0010 Promoter] and [http://parts.igem.org/Part:BBa_B0034 RBS BBa_B0034 ]. The sequence can be found here. [http://parts.igem.org/Part:BBa_K1763001 BBa_K1763001 ] along with further details on the design and cloning of this biobrick.

Protein Expression

• We have just finished our first round of honey bee silk expression from [http://parts.igem.org/Part:BBa_K1763001 BBa_K1763001]
• Here is our first attempt at protein expression along with the gel.

Fig. 1 Expected size of product is 31.6 kDA

• • Unfortunately the purified protein that we see on the gel (should be in next to last lane on the right) doesn't seem to be the right size.
  • We will try again using a T7 promoter and a slightly modified protein expression and purification protocol.

What we are working on now

• We are currently at the starting phases of honeybee silk protein expression. We have expressed [http://parts.igem.org/Part:BBa_K1763001 BBa_K1763001 ]. The protein we purified is not super clean and does not seem to be the right size. We are about to try again using a T7 promoter. Right now we are in the process of cloning our silk gene into a pET expression vector with a T7 promoter. For our progress so far, see our lab notebook entries from 5/18,5/19, and 5/26 for our first attempts at protein expression. And see our entries from 5/30, 7/10, 7/12, 7/13, 7/15, and 7/16 for progress on cloning honeybee silk protein into our t7 backbone.
• One of our sequencing reactions checked out for the silk in the pet 24a expression vector, although with 2 silent mutations. We'll take it though!
• Update as of 7/23. We have sequence verified our silk construct in our e coli expression strain, BL21. We can now proceed to expression with our new and improved t7 promoter system!

Raw lab notebook entries

• April 28 - May 6 = cloning of [http://parts.igem.org/Part:BBa_K1763000 BBa_K1763000] and [http://parts.igem.org/Part:BBa_K1763001 BBa_K1763001 ]
• May 16-May 19 = Expressing Silk Protein in E. Coli.
• May 26-27 = Purifying Silk Protein
• July 10-16 = Cloning Silk into Pet vector and preparing BL21 (DE3) competent cells