Composite

Part:BBa_K3028000

Designed by: Yulia Kacher   Group: iGEM19_Moscow   (2019-10-14)
Revision as of 10:05, 16 October 2019 by Juliakacher (Talk | contribs)


N-terminal part of beta-lactamase fused with dCas9 and double terminator

N-terminal part of beta-lactamase fused with dCas9 and double terminator

Part BBa_K1689013 is an N-terminal fragment of β-lactamase fused with dCas9. dCas9 enzyme is also known as a catalytically dead Cas9 enzyme[1]. It lacks traditional endonuclease activity (it does not cleave DNA) but preserves its ability to bind targets very specifically. This part was modified by IGEM_Peking team for DNA detection purposes. β-Lactamases - bacterial enzymes that can hydrolyze the amide bond of the β-lactam ring, hence inactivate β-lactam antibiotics (AmpR). Split β-Lactamase (196|198) [2] is used as a reporter, for example, to study different protein-protein interactions. When fused to dCas9, it can report the presence of a specific target by regaining its enzymatic activity.

Our part is a composition of the most commonly used terminator and BBa_K1689013. It was necessary to make such an improvement, because of all side effects of Cas synthesis for cells.


[1] Repurposing CRISPR As An RNA-Guided Platform For Sequence-Specific Control Of Gene Expression. Qi, L. S., Larson, M. H., Gilbert, L. A., Doudna, J. A., Weissman, J. S., Arkin, A. P., and Lim, W. A. 2013, Cell Vol. 152, pp. 1173-1183.

[2] Beta-lactamase complementation assays as in vivo and in vitro sensors of protein–protein interactions Galarneau A, Primeau M, Trudeau L, Michnick S; Nature Biotechnology; 2002 vol: 20 (6) pp: 619-622

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1693
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 4
    Illegal BamHI site found at 3972
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


[edit]
Categories
Parameters
None