mVenus, MocloMania B5
This part codes for the yellow fluorescent protein with the poetic name mVenus. It is a deviation of the famous green fluorescent protein GFP originally isolated from the bioluminescent jellyfish Aequorea victoria in 1962. By coupling a protein of interest with a fluorescent tag such as mVenus, the target protein can be easily and non-invasively detected within living cells as well as cell preparations with the help of fluorescence spectroscopy and microscopy. As a B5 part, this part is meant to occupy the most downstream position in the MocloMania cloning frame and is thus equipped with an additional stop codon.
size 26.9 kDa
function fluorescent tag
excitation wavelength 515 nm
emission wavelength 537 nm
cloning position B5
plasmid backbone pAGM1301
We were able to successfully clone this basic part into its respective L0 plasmid backbone and to confirm the integrity of the L0 construct via restriction digest and gel electrophoresis, see Figure 1. Furthermore, we were able to include it into a L1 construct, proving its correct adaptation towards MoClo assembly, see Figure 2.
Several different L1 constructs assembled with L0_mVenus_B4 have been successfully transfected into Leishmania, resulting in recombinant protein expression that could be observed after immunostaining on western blot.
Looking at Figure 3, we see that construct 1 | L1_sAP_RBD_mVenus shows definite protein bands in the culture supernatant when stained against the SARS-CoV-2 receptor binding domain. These bands display a high signal intensity and run at about 30 kDa, 35 kDa and 70 kDa. This is contradictory to the molecular size predicted in silico where the full-length fusion protein weighs about 50 kDa. Since the band pattern closely resembles the one seen in other fluorophore carrying constructs, e.g. L1_sAP_RBD_mCerulean, we assume that this size shift is caused by technical deficiencies of the SDS-PAGE conduct. Shift of bands to unexplicably higher sizes might stem from a problem in gel density, caused for example by excess acrylamide concentrations.
Since the upper band of construct 1 is attributed to the full-length fusion protein, the smaller bands' origin needs to be hypothesized. Since however the most prominent lower band runs around 28 kDa and can be observed by staining against RBD, this suggests that extracellular cleavage processes might separate RBD and fusion tags after secretion of the fusion protein into the culture medium. For more information on this, please consult the sAP secretion tag part site.
The second construct employing L0_mVenus_B5, 3 | L1_3xHA_RBD_mVenus, shows only a very faint band that corresponds to the in silico predicted size of the fusion protein. Since the construct does not contain a sAP secretion tag, detection of protein expression is limited to the cell lysate P+.
So far, none of the L1 constructs employing a C-terminal mVenus have been successfully purified. Furthermore, fluorescence screenings of cells producing recombinant mVenus have not yet been conducted. Thus, at this point in time, functionality of the mVenus fusion tag cannot be definitively verified. We are working hard on optimizing expression and purification yields in order to finalize part validation and implementation towards their respective functionality.
The MocloMania collection
This basic part is part of the MocloMania collection, the very first collection of genetic parts specifically designed and optimized for Modular Cloning assembly and recombinant protein expression in the protozoan parasite Leishmania tarentolae.
Are you trying to express complexly glycosylated proteins? Large antibody side chains? Human proteins that require accurate post-translational modification? Then Leishmania might be just the right organism for you! Leishmania tarentolae’s glycosylation patterns resemble those of human cells more closely than any other microbial expression host, while still delivering all the benefits of microbial production systems like easy transfection and cultivation. So instead of relying on mammalian cell lines, try considering Leishmania as your new expression host of choice!
Our MocloMania collection will allow you to easily modify your protein of choice and make it suitable for downstream detection and purification procedures - all thanks to the help of Modular Cloning. This cloning system was first established by Weber et al. in 2011 and relies on the ability of type IIS restriction enzymes to cut DNA outside of their recognition sequence, hereby generating four nucleotide overhangs. Every basic part in our collection is equipped with a specified set of overhangs that assign it to its designated position within the reading frame. These so-called cloning positions are labelled B2-B5 from upstream to downstream. By filling all positions with the basic parts of your choice, you can easily generate variable genetic constructs that code for the fusion protein of your desire.
We furthermore provide a specifically domesticated Leishmania expression vector, named weird_plex, which will package your fusion construct into a functional transcriptional unit that is optimized for high expression in Leishmania.
The best part? Because of the type IIS restriction properties and the specifity of the generated overhangs, restriction and ligation of your construct can all happen simultaneously in a simple one-step, one-pot reaction. This will safe you a lot of time and frustration in your cloning endeavours!
Do we have your attention? In the table below you can find some basic information on how our cloning system, along with most other MoClo systems, is set up. Please feel free to check out our wiki to find more information on Leishmania and Modular Cloning as well as to understand how this basic part integrates into our part collection. See you there!
|Level||What does this level contain?||antibiotic resistance||Enzyme used for ligation|
|L0||The foundation to every MoClo construct which are basic genetic units, such as coding sequences, promoters, terminators||spectinomycin||BbsI|
|L1||Several L0 parts assembled into a functional transcriptional unit, e.g. consisting of promoter, coding region and terminator||ampicillin||BsaI|
|L2||Multiple transcriptional units added into one multi-gene construct, e.g. a protein of interest fused to a resistance cassette||kanamycin||BbsI|
Sequence and Features
- 10Illegal PstI site found at 202
- 12Illegal PstI site found at 202
- 21COMPATIBLE WITH RFC
- 23Illegal PstI site found at 202
- 25Illegal PstI site found at 202
Illegal NgoMIV site found at 679
- 1000COMPATIBLE WITH RFC
- Gert-Jan Kremers, Joachim Goedhart, Erik B. van Munster, and Theodorus W. J. Gadella. Cyan and Yellow Super Fluorescent Proteins with Improved Brightness, Protein Folding, and FRET Förster Radius, Biochemistry 2006 45 (21), 6570-6580, DOI: 10.1021/bi0516273
- Shimomura, O., Johnson, F.H. and Saiga, Y. (1962) Extraction, Purification, and Properties of Aequorin, a Bioluminescent Protein from the Luminous Hydromedusan, Aequorea. Journal of Cellular and Comparative Physiology, 59, 223-239. http://dx.doi.org/10.1002/jcp.1030590302
- M.A. Rizzo, D.W. Piston High-contrast imaging of fluorescent protein FRET by fluorescence polarization microscopy Biophys. J., 88 (2005), pp. L14-L16
- Langer T, Corvey C, Kroll K, Boscheinen O, Wendrich T, Dittrich W. Expression and purification of the extracellular domains of human glycoprotein VI (GPVI) and the receptor for advanced glycation end products (RAGE) from Rattus norvegicus in Leishmania tarentolae. Prep Biochem Biotechnol. 2017 Nov 26;47(10):1008-1015. doi: 10.1080/10826068.2017.1365252. Epub 2017 Aug 31. PMID: 28857681.
- Weber E, Engler C, Gruetzner R, Werner S, Marillonnet S (2011) A Modular Cloning System for Standardized Assembly of Multigene Constructs. PLoS ONE 6(2): e16765. https://doi.org/10.1371/journal.pone.0016765
|biology||yellow fluorescent protein|