Difference between revisions of "Part:BBa K1399007"
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=2019 OUC-China's characterization= | =2019 OUC-China's characterization= | ||
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==Background== | ==Background== | ||
+ | This part was GFP(mut3b) followed by a variation of the WT SsrA tag sequence, which codes for the amino acid sequence AANDENYNYADAS. When the degradation tag fused to the C-terminal of proteins, it will make the protein susceptible to fast degradation through SspB-mediated binding to the ClpX protease as well as ClpA. DAS variants of SsrA tags require SspB for efficient degradation. | ||
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==Result== | ==Result== |
Revision as of 19:56, 15 October 2019
GFP (mut3b) with SsrA-DAS+2 degradation tag
GFP (mut3b) (Part:BBa_E0040) with added engineered NYADAS-ssrA degradation tag (Part:BBa_M0051). The tag increases GFP turn-over rate, thus providing better temporal resolution of green fluorescence. In the same time, maximal fluorescence amplitudes will be lower as newly formed protein is degraded as soon as it is formed.
SsrA tags encode peptide sequence that is recognized by ClpA and ClpX unfoldases and ClpX mediator SspB (Figure 1).[1]
ClpA and ClpX then form a proteosome-like complex with ClpP protease and the protein is degraded.[1] The final three residues of the tag determines the strength of interaction with ClpX and thus the final protein degradation rate.[2] The NYADAS tag encodes peptide sequence AANDENYNYDAS is reported to have low affinity to ClpX thus its mediated degradation very much depends on the concentration of SspB (ClpX mediator).[1] The two additional residues ‘NY’ extends tag between SspB and ClpX binding sites, thus preventing clash when both proteins are bound to the tag.[3] However, be aware that exact protein degradation rate is influenced by multiple other factors: ClpXP and ClpAP protease concentrations, protein stability, Km of binding to the protease, temperature [4].
Contents
References
[1] Flynn, J. M. et al. Overlapping recognition determinants within the ssrA degradation tag allow modulation of proteolysis. Proc. Natl. Acad. Sci. U. S. A. 98, 10584–9 (2001).
[2] Andersen, J. B. et al. New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Appl. Environ. Microbiol. 64, 2240–6 (1998).
[3] McGinness, K. E., Baker, T. a & Sauer, R. T. Engineering controllable protein degradation. Mol. Cell 22, 701–7 (2006).
[4] Purcell, O., Grierson, C. S., Bernardo, M. Di & Savery, N. J. Temperature dependence of ssrA-tag mediated protein degradation. J. Biol. Eng. 6, 10 (2012).
2019 OUC-China's characterization
Background
This part was GFP(mut3b) followed by a variation of the WT SsrA tag sequence, which codes for the amino acid sequence AANDENYNYADAS. When the degradation tag fused to the C-terminal of proteins, it will make the protein susceptible to fast degradation through SspB-mediated binding to the ClpX protease as well as ClpA. DAS variants of SsrA tags require SspB for efficient degradation.
Result
Protocol
Extend to our project
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 644