Part:BBa_K3815033

HIV-1 reverse transcriptase p51

Description of this part

Targeted protein

Fig1. From left to right: 1-4: newly prepared homemade RT with different enzyme concentrations, 5: no enzyme, 6: Bst3.0, 7: old homemade RT, 8: no template control

This part is used to purify homemade Reverse Transcriptase. This is derived from HIV-1(Human Immunodeficiency Virus). This enzyme is more thermotolerant than normal reverse transcriptase, making it useful for LAMP(Loop-Mediated Isothermal Amplification)) and RT-LAMP(Reverse Transcription Loop-Mediated Isothermal Amplification). A peptide made from one ORF is partially digested in an infected cell and becomes two fragments, p66 and p51. It is known that the HIV-1 RT functions when the p66 and p51 form a heterodimer. To purify them as recombinant proteins in E.coli, we separately expressed and purified p66 and p51, and dimerized them in vitro before use. This part is to express p51. We examined our homemade reverse transcriptase activity in vitro. We used total yeast DNA/RNA for this assay. We selected the intron-containing region of Rpl19A as a template for reverse transcription. If there is no reverse transcription, the genomic DNA including an intron is amplified by PCR, resulting in a band of 876 bp. On the other hand, if cDNA is correctly synthesized by reverse transcription, a band of 370 bp without an intron should appear. As shown below, the cDNA band was successfully observed in an RT-dependent manner. From this result, we concluded the activity of homemade RT.

Sequence and Features

Assembly Compatibility:

• 10
  INCOMPATIBLE WITH RFC[10]

  Illegal PstI site found at 320
  
• 12
  INCOMPATIBLE WITH RFC[12]

  Illegal PstI site found at 320
  
• 21
  COMPATIBLE WITH RFC[21]
• 23
  INCOMPATIBLE WITH RFC[23]

  Illegal PstI site found at 320
  
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal PstI site found at 320
  Illegal AgeI site found at 966
  
• 1000
  COMPATIBLE WITH RFC[1000]

Purification

Fig2. SDS-PAGE of purified proteins

Expression

• Cells were cultivated in 1000ml LB media at 37^oC shaking at 180 rpm to the log-phase.
• when the OD600 reaches 0.35-0.7, IPTG was added at the final concentration of 0.5mM to induce the peptide expression.
• After 3 hours of induction, cells were harvested and frozen in liquid-N2.
• We added purified p66(BBa_K3815034) and p51(BBa_K3815033) to the same tube and incubated them at -30^oC for 4 days to make a dimer.

Purification

After the cell disruption by sonication, each protein was purified using Ni-NTA beads. Samples were eluted by a four-step gradient of Imidazole.(70mM, 95mM, 120mM, 270mM)

Fig2 shows the result of SDS-PAGE. The lane 5,6,7,8 are the result of Reverse Transcriptase.
We observed the correct bands in the SDS-PAGE gel. The arrowheads indicate the targeted proteins.

Reference

https://www.biorxiv.org/content/10.1101/2020.06.23.166397v2.full.pdf