Part:BBa_K3781004

3xHA, MocloMania B2

This basic part codes for a 3xHA epitope tag that can be used for western blot detection of your fusion protein. It is based on the HA epitope tag first established in 1988 by J. Field and colleagues which is derived from a small segment of the viral protein hemagglutinin (HA), one of three integral membrane proteins in the Influenza A virus., Fusing your protein of interest with a 3xHA-tag enables its detection using inexpensive commercial primary antibodies against the HA epitope and thus eliminates the need for expensive protein-specific antibodies.

size 3.56 kDa

function antibody detection tag

amino acid sequence YPYDVPDYA GS YPYDVPDYA GS YPYDVPDYA

cloning position B2

plasmid backbone pAGM1276

Data

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.

• 

  Figure 1 | Test digest of L0-3xHA_B2 using BstEII and SapI
  1 | L0_3xHA_B2 | 1563 + 583 + 201 bp
  L | Thermofischer GeneRuler Plus Ladder [bp]
• 

  Figure 2 | Test digest of L1 constructs using SacI
  1 | L1_3xHA_RBD_mVenus | 6098 + 2515 bp
  2 | L1_3xHA_RBD_mCerulean | 6098 + 2515 bp
  3 | L1_sAP_RBD_mVenus | 6071 + 2515 bp
  4 | L1_sAP_RBD_mCerulean | 6071 + 2515 bp
  L | Thermofischer GeneRuler Plus Ladder [bp]

While L0_3xHA_B2 has been used to assemble several different L1 constructs, only one of them, L1_3xHA_RBD_mCerulean, has been transfected into Leishmania and showed significant protein expression after <b>immunostaining on western blot, see Figure 3.

• 

  Figure 3 | Immunoblot of L1 transfected Leishmania cell cultures | stained against RBD
  1 | L1_sAP_RBD_mCerulean | 51.9 kDa
  2 | L1_sAP_RBD_mCerulean_Strep8His | 54.3 kDa
  3 | L1_sAP_RBD_mCerulean_GST | 78.6 kDa
  4 | L1_3xHA_RBD_mCerulean | 55.7 kDa
  n.c. | negative control | Leishmania culture
  transfected with empty L1 expression vector
  p.c. | RBD-GFP | 54 kDa
  L | Thermofischer PageRuler Protein Ladder [kDa]
  1. AB | ms anti-RBD
  2. AB | rb anti-ms HRP
  

When looking at construct 4 | L1_3xHA_RBD_mCerulean, a single protein band can be detected in the cell lysate P+. Taking into consideration any gel deficiencies influencing electrophoresis, this band can be attributed to the full-lenght fusion protein calculated to weigh about 55.7 kDa. Since no secretion tag was included in the construct, protein expression was exclusively observed within the cell lysate. So far, no immunoblot staining against the HA epitope has been conducted. Thus, the functionality of L0_3xHA_B2 could not yet be definitively verified. We are working hard on realizing this experiment in order to qualitatively validate the functionality of this basic part.

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 the part that you are looking at integrates into our part collection. See you there!

MOCLO | Important nomenclature and parameters

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 selection marker	kanamycin	BbsI

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]