Difference between revisions of "Team:Peking/Basic Part"

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                                     Fig. 1. Basic structure of the following parts
 
                                     Fig. 1. Basic structure of the following parts
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                                     Fig. 2. 3A: Triple spytag SUP: Super uranyl-binding protein
 
                                     Fig. 2. 3A: Triple spytag SUP: Super uranyl-binding protein
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                                     Fig. 3. 3B Triple spycatcher
 
                                     Fig. 3. 3B Triple spycatcher
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                                     Fig. 4. 3A: Triple spytag mSA: Monomeric streptavidin
 
                                     Fig. 4. 3A: Triple spytag mSA: Monomeric streptavidin

Revision as of 12:45, 19 October 2016

Parts

Parts

Favorite Parts

Fig. 1. Basic structure of the following parts

BBa_K1989000

Fig. 2. 3A: Triple spytag SUP: Super uranyl-binding protein

Super uranyl-binding protein (SUP) was fused to 4*(VPGVG) spaced triple spytag. The fused protein is used to generate the uranyl-binding capacity in our hydrogel system. Paired with triple spycatcher (BBa_K1989001) and tripled spytag with mSA (BBa_K1989002) our hydrogel system is constructed.


BBa_K1989001

Fig. 3. 3B Triple spycatcher

Triple spycatcher was spaced by 15*(VPGVG). Paired with triple spytag (BBa_K1989000) and tripled spytag with mSA (BBa_K1989002) our hydrogel system is constructed.

BBa_K1989002

Fig. 4. 3A: Triple spytag mSA: Monomeric streptavidin

Monomeric streptavidin (mSA) was fused to 4*(VPGVG) spaced triple spytag. The fused protein is used to generate the recyclable capacity in our hydrogel system. Paired with triple spycatcher (BBa_K1989001) and tripled spytag with SUP (BBa_K1989000) our hydrogel system is constructed.


Part Table

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Part Collection

2016 Peking iGEM team members devoted themselves to constructing a part library of the multifunctional material. We have not only submitted all of new basic Spy network parts, but also provided multiple composite parts combining Spy network with other metal binding proteins and fluorescent proteins. We also constructed a library of signal peptides and validated the secretion capacity of our material.

Functions of all the parts were tested and validated both in controlled laboratory condition and in normal condition. The parts allow simple modules insertion using 3A Assembly, Gibson and Golden Gate Assembly which making them convenient and powerful tools for other iGEM team.