Difference between revisions of "Part:BBa K3168007"

Revision as of 12:14, 17 September 2019

dCas9-BRET

This composite part is made up of two basic parts. The first basic part (BBa_K3168001) codes for a catalytically dead CRISPR associated protein 9 (dCas9) which is circularly permutated and only contains one cysteine (S867C) at the HNH domain to enable dye incorporation via maleimide coupling (Sternberg, 2015). dCas9 binds to a specific target on double stranded DNA. This specific target is determined by the guide RNA, which makes the target sequence of this protein very modular. The second basic part (BBa_K3168006), which is fused to dCas9, consist of a (SGG)2 linker and cysteine free NanoLuc. A Cy3 dye can be incorporated at S867C via maleimide coupling.

Usage and Biology

When a Cy3 dye is incorporated, the conformational change of the HNH domain when dCas9 binds to DNA can be detected. In the presence of the substrate (Furimazine), blue light is emitted by NanoLuc. The emission spectrum of NanoLuc overlaps with the excitation spectrum of Cy3. When this fusion protein binds to its target, a conformational change occurs which brings the Cy3 dye close to NanoLuc. This enables bioluminescent resonance energy transfer (BRET), which causes the emission of red light.

Figure 1. Schematic representation dCas9-BRET system.

References

Oakes, B. L., Fellmann, C., Rishi, H., Taylor, K. L., Ren, S. M., Nadler, D. C., ... & Savage, D. F. (2019). CRISPR-Cas9 circular permutants as programmable scaffolds for genome modification. Cell, 176(1-2), 254-267.

Sternberg, S. H., LaFrance, B., Kaplan, M., & Doudna, J. A. (2015). Conformational control of DNA target cleavage by CRISPR–Cas9. Nature, 527(7576), 110.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
INCOMPATIBLE WITH RFC[12]
Illegal NheI site found at 2143
21
INCOMPATIBLE WITH RFC[21]
Illegal BamHI site found at 261
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

@@ Line 1: / Line 1: @@
 __NOTOC__
-<partinfo>BBa_K3168007 short</partinfo>
+===dCas9-BRET===
 This composite part is made up of two basic parts. The first basic part (BBa_K3168001) codes for a catalytically dead CRISPR associated protein 9 (dCas9) which is circularly permutated and only contains one cysteine (S867C) at the HNH domain to enable dye incorporation via maleimide coupling (Sternberg, 2015). dCas9 binds to a specific target on double stranded DNA. This specific target is determined by the guide RNA, which makes the target sequence of this protein very modular. The second basic part (BBa_K3168006), which is fused to dCas9, consist of a (SGG)2 linker and cysteine free NanoLuc. A Cy3 dye can be incorporated at S867C via maleimide coupling.
-<!-- Add more about the biology of this part here
 ===Usage and Biology===
+When a Cy3 dye is incorporated, the conformational change of the HNH domain when dCas9 binds to DNA can be detected. In the presence of the substrate (Furimazine), blue light is emitted by NanoLuc. The emission spectrum of NanoLuc overlaps with the excitation spectrum of Cy3. When this fusion protein binds to its target, a conformational change occurs which brings the Cy3 dye close to NanoLuc. This enables bioluminescent resonance energy transfer (BRET), which causes the emission of red light.
+[[File:T--TU_Eindhoven--dCas9-BRET.png|400px|]]
+'''Figure 1. Schematic representation dCas9-BRET system.'''
+===References===
+Oakes, B. L., Fellmann, C., Rishi, H., Taylor, K. L., Ren, S. M., Nadler, D. C., ... & Savage, D. F. (2019). CRISPR-Cas9 circular permutants as programmable scaffolds for genome modification. Cell, 176(1-2), 254-267.
+Sternberg, S. H., LaFrance, B., Kaplan, M., & Doudna, J. A. (2015). Conformational control of DNA target cleavage by CRISPR–Cas9. Nature, 527(7576), 110.
 <!-- -->