From 2007.igem.org

A single-protein calcium ion sensor mediating cell survival

Introduction

The idea:
Was to attach enzyme-halfs to several trigger-proteins (here: calmodulin) by cloning each one of the enzyme-halfs and the trigger-protein together in one plasmid.
This plasmid would then contain the code for the whole "protein-machinery", allowing in vivo-tests as well as expression and purification of the engineered protein, an on/off-switchable enzyme.

DHFR Calmodulin Ca2+ sensor. Image adapted from Truong et al. 2001

Split enzymes:
Some enzymes can be divided into two separate parts that don´t show any activity until both parts are physically brought together;
this circumstance allows enzyme-activity-assays.
As those assays were already being used in our lab before, we could access plasmids containing enzyme-halfs of beta-lactamase and dihydrofolatereductase (DHFR).

Calmodulin:
This molecule is known for its strong conformational change upon binding calcium.
Truong, Ikura et al.(Ontario Cancer Institute and [http://medbio.utoronto.ca/ Department of medical Biophysics] , University of Toronto) have fused CFP and YFP to the ends of modified calmodulin and shown that you can then induce [http://en.wikipedia.org/wiki/Fluorescence_resonance_energy_transfer FRET] between them by adding calcium.
This work inspired us to test calmodulin as "switch" for our split enzymes. Prof. Ikura/ Le Zheng were so friendly to send us this calmodulin (YC6.1 in plasmid pcDNA3 with sequence, thanks a lot again!) so that we could gain it via PCR.

Picture: DHFR1(pink)-Calmodulin(green)-DHFR2(blue)-Construct, active state; calcium bound

Picture: DHFR1(pink)-Calmodulin(green)-DHFR2(blue)-Construct, inactive state; no calcium bound

Materials and Methods

Planning:
-Plasmid maps, sequences, alignments and protein dates have been worked out using "gcg", a unix-based, rather antiquate genetic engineering program
-3D-Models of our constructs (as shown in the pictures above) have been created/modified using (Mac-)Pymol and SwissPdbViewer (both freeware:[http://pymol.sourceforge.net/ Pymol],[http://expasy.org/spdbv/ SwissPdbViewer])

Cloning:
-Cloning steps have been done as described under protocols or with Qiagen-products

Protein expression and purification:
-Expression cultures (Volume: 2 liters) have been raised at 37 deg. C and induced by IPTG
-Protein purifications have been carried out via Ni-NTA-columns; the His-Tagged proteins have been eluted in buffers with rising imidazole-concentrations and were then analyzed on SDS-gels

Picture: Growth of E.coli with DHFR1-4Gly-Calmo-4Gly-DHFR2A in minimal medium at different Ca2+-concentrations

Results

Plasmids:
We gained plasmids containing both parts of DHFR, linked to calmoduline by 2/4/6 glycins each; in-vivo-growth tests showed the best activity for 4-glycine linkers;
thus we decided to proceed with this linker-length.

In-Vivo-Analysis:
As DHFR is essential for bacterial growth in minimal medium with trimethioprim (TMP), we could show that the ability of E.colis with our plasmid to grow is directly dependant on the presence -and, furthermore, concentration- of calcium-ions (Ca2+)in the medium:In vivo test II:
In this test we inoculated M9 minimal medium at different calcium concentrations with DHFR1-4Calmodulin4-DHFR2A-positive E. colis and measured the absorptions (first measurement after 24 hours and then again every three to 10 hours for another two days/ 50 hours). Several tests we performed before made this approach seem best.

Discussion

Our goal to create a fusion-protein sensor with functional nano-mechanical aspects seems to be achieved at least for DHFR.
As far as beta-lactamase is concerned we encountered various problems cloning together the plasmid we had planned to as the product seemed to toxify E. coli.For this reason, the lactamase-parts we have submitted are optimized to enhance stability.

Parts submitted

References

split DHFR:

Pelletier JN, Arndt KM, Plückthun A, Michnick SW. "An in vivo library-versus-library selection of optimized protein-protein interactions." Nat Biotechnol. 1999 Jul;17(7):683-90.

Pelletier JN, Campbell-Valois FX, Michnick SW. "Oligomerization domain-directed reassembly of active dihydrofolate reductase from rationally designed fragments." Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12141-6. [http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSearch=9770453&ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum pubmed]

Calmodulin Sensor:

Pham E, Chiang J, Li I, Shum W, Truong K "A computational tool for designing FRET protein biosensors by rigid-body sampling of their conformational space." Structure. 2007 May;15(5):515-23.

Truong K, Sawano A, Miyawaki A, Ikura M. "Calcium indicators based on calmodulin-fluorescent protein fusions." Methods Mol Biol. 2007;352:71-82.

Truong K, Sawano A, Mizuno H, Hama H, Tong KI, Mal TK, Miyawaki A, Ikura M. "FRET-based in vivo Ca2+ imaging by a new calmodulin-GFP fusion molecule." Nat Struct Biol. 2001 Dec;8(12):1069-73.

Reviews on calmodulin: Grabarek Z "Structural basis for diversity of the EF-hand calcium-binding proteins." J Mol Biol. 2006 Jun 9;359(3):509-25.

Soderling TR, Stull JT "Structure and regulation of calcium/calmodulin-dependent protein kinases." Chem Rev. 2001 Aug;101(8):2341-52

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