Difference between revisions of "Team:Slovenia/Protease signaling/Reporters"

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<x-ref>Conti</x-ref>.
 
<x-ref>Conti</x-ref>.
 
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<img onclick="resize(this);" class="ui medium image" src=" https://static.igem.org/mediawiki/2016/0/08/T--Slovenia--4.5.1.png" >
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<figcaption><b>Proteolytic activity determined by the cpLuc reporters.</b><br/>
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HEK293T cells were transfected with 100ng of indicated reporter constructs and 70ng of their corresponding proteases. Luciferase activity was measured 24h after transfection. The results are presented as normalized firefly luciferase activity (RLU).</figcaption>
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<p>The circularly permutated luciferase makes use of this requirement for a conformational change by rearranging the sequence of the protein. The permutation is obtained
 
<p>The circularly permutated luciferase makes use of this requirement for a conformational change by rearranging the sequence of the protein. The permutation is obtained
 
by placing the C-terminal region of the protein (amino acids 234-544) upstream of the N-terminal region (amino acids 4-233) and connecting them by a short linker  
 
by placing the C-terminal region of the protein (amino acids 234-544) upstream of the N-terminal region (amino acids 4-233) and connecting them by a short linker  
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relatively low, compelling us to look for another reporter.
 
relatively low, compelling us to look for another reporter.
 
</p>
 
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<figure data-ref="2">
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<img onclick="resize(this);" class="ui medium image" src=" https://static.igem.org/mediawiki/2016/0/08/T--Slovenia--4.5.1.png" >
+
<figcaption><b>Proteolytic activity determined by the cpLuc reporters.</b><br/>
+
HEK293T cells were transfected with 100ng of indicated reporter constructs and 70ng of their corresponding proteases. Luciferase activity was measured 24h after transfection. The results are presented as normalized firefly luciferase activity (RLU).</figcaption>
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</figure>
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Revision as of 23:07, 15 October 2016

Reporters

nbsp;Reporters

As our project was aimed develop novel orthogonal signaling pathways based on proteases, as well as at the development of the protein ER retention and release system, we tested and adapted several types of reporters, that will be useful for other iGEM teams.

To measure the activity of the proteases we used three types of reporters based on the firefly luciferase: the cleavable fLuc, the circularly permutated fLuc (cpLuc) and the cyclic fLuc (cycLuc). Additionally, we developed a split luciferase system that functions as an output of logic gates, which integrated the activity of orthogonal proteases.

Finally, to measure the ER protein retention and release, we used TagRFP and SEAP reporters.

Luciferase reporter of the proteolytic activity can be designed either to lead to the decrease of its activity due to proteolysis or to generate the activity by cleavage. Cleavable luciferase assay is expected to be relatively insensitive as it can only detect if a large fraction of the luciferase has been degraded, typically more than 20%, while an assay that leads to the activation of the luciferase might be able to detect much smaller fraction of the proteolytic cleavage.

Cleavable luciferase


Into the loop of the firefly luciferase (fLuc) we inserted amino acid sequence that is targeted by proteases. The substrate sequence thus divided the fLuc into two fragments (nLuc and cLuc), with a protease cleavage site between them (1A and B). The insertion site for the substrate sequence was based on the previously described split luciferase system Shekhawat2009, where we expected that this site would also be permissible to short linker insertion without significantly altering luciferase activity. Upon addition of an appropriate protease, the reporter would be cleaved at the substrate site and the two fragments would dissociate and in turn decrease the fLuc activity. In this system higher protease activity corresponds to a lower luciferase activity. The reporters were additionally equipped with a protein tag at the N-terminal and C-terminal end in order to allow immunostaining to detect protein cleavage by the western blot (1).

INSERT!!

Circularly permuted luciferase


The first reporter to measure protease activity that results in the generation of the luciferase activity by the proteolytic cleavage was a circularly permuted version of the firefly luciferase (cpLuc). Luciferase is an oxidative enzyme that produces bioluminescence. The protein consists of two compact domains: the larger N- and the smaller C-terminal domain. The C-terminal domain is connected to the N-terminal domain by a flexible hinge. When bound to the substrate luciferin, luciferase has to undergo a conformational change from an open to a closed form with the two domains coming together to enclose the substrate and efficiently catalyze its oxidation Conti.

Proteolytic activity determined by the cpLuc reporters.
HEK293T cells were transfected with 100ng of indicated reporter constructs and 70ng of their corresponding proteases. Luciferase activity was measured 24h after transfection. The results are presented as normalized firefly luciferase activity (RLU).

The circularly permutated luciferase makes use of this requirement for a conformational change by rearranging the sequence of the protein. The permutation is obtained by placing the C-terminal region of the protein (amino acids 234-544) upstream of the N-terminal region (amino acids 4-233) and connecting them by a short linker (1C and D), which contains a protease cleavage site Fan2008. This linker prevents the conformational change required for the efficient catalysis; therefore, the catalytic cycle is triggered only upon cleavage of the linker by a protease.

Activity of the cpLuc depended on the protease cleavage for all four tested proteases as expected (2), however light emission from this reporter system was relatively low, compelling us to look for another reporter.