Part:BBa_K3610032
BAK1 ectodomain / YFP
This part contains the ectodomain of the plant cell surface receptor from A. thaliana fused to a yellow fluorescent protein. This part lacks the natural N-terminal signal sequence but instead uses the signal sequence from the alpha-Factor from yeast.
Usage and Biology
BAK1
The BRI1-associated receptor kinase (BAK1) is a leucin-rich repeat receptor kinase (LRR-RK) which interacts with multiple other LRR-RKs with different functions in hormone signalling and defense response. BAK1 localizes at the plasma membrane and the endosome. The BAK1 protein forms a structure with an extracellular domain with leucin-rich repeats, a single pass transmembrane domain and an intracellular domain with a kinase function.
Among others, BAK1 interacts with the LRR-RKs EF-Tu receptor (EFR), Flagellin sensing 2 (FLS2) and cold-shock protein receptor (CORE), all of which are pathogen recognition receptors (PRR) in brassicaceae plants. Upon binding of a microbe-associated molecular pattern at the LRR domain of the PRR, BAK1 forms a heterodimer with the PRR which triggers a phosphorylation cascade, leading to upregulation of defense mechanisms.
BAK1 fused to YFP
In this sequence, the C-terminal domain entailing the intracellular kinase domain was replaced with the sequence coding for the yellow fluorescent protein venus, while the ectodomain and the transmembrane domain, including the juxtamembrane domain were kept. Additionally, a signal sequence native to S. cerevisiae was fused to the N-terminal sequence, which does not contain the native signal peptide. This way, the protein can be integrated into the membrane during translation. Additionally, the YFP (Exλ : 515 nm, Emλ : 528 nm) gets translated together with the receptor protein, which allows observation of expression and localization under a microscope and measurement of the strength of the expression with a fluorometer.
Characterization
Expression of BAK1/YFP in S. cerevisiae
After successful transformation of yeast cells we checked for expression of the protein under a confocal microscope.
Confocal microscopy confirmed increased fluorescence in the S. cerevisiae cells that had been previously transfected with plasmids containing BAK1 ectodomain fused to YFP. This increased fluorescence indicates expression of our genes. Additionally, this imaging experiment revealed that the fluorescent protein is in part localized at the cell periphery. This is in alignment with our expectations as our construct includes a secretion signal protein and a receptor coding protein with the transmembrane domain.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 867
Illegal PstI site found at 912 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 867
Illegal PstI site found at 912 - 21INCOMPATIBLE WITH RFC[21]Unknown
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 867
Illegal PstI site found at 912 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 867
Illegal PstI site found at 912 - 1000COMPATIBLE WITH RFC[1000]
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