Haynes:LCR Assembly

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LCR - Ligase Cycling Reaction

by Karmella Haynes and Cameron Gardner, 2015
Based on de Kok, S., Stanton, L. H., Slaby, T., Durot, M., Holmes, V. F., Patel, K. G., et al. (2014). Rapid and reliable DNA assembly via ligase cycling reaction. ACS synthetic biology, 3(2), 97–106. doi:10.1021/sb4001992

<fint color="red">DRAFT

Principle: The DNA parts to be assembled are blunt-ended PCR products (generated by Phusion polymerase). 5' phosphates are added by polynucleotide kinase or 5'-phos primers. After (initial) denaturation at high temperature, the upper (or lower) strands of neighboring DNA parts anneal with non-phosphorylated bridging oligos, complementary single-stranded DNAs that span the junctions between adjacent DNA parts. Thermostable ligase joins the DNA backbones via a phosphodiester bond without introducing any scar sequences. In subsequent denaturation−annealing−ligation temperature cycles, the bridging oligos are replaced by complementary strands from the DNA parts and that backbone is sealed. By applying multiple temperature cycles, many DNA parts can be assembled into complex DNA constructs.

Part 1: Prep the Oligo Bridges

• Note: Final conc. in LCR rxn. is 30 nM each

1. Bring the IDT oligo pellet to 100μM with dH₂O. nmoles oligo (on label) * 10 = μL H₂O to add
2. Make a 300 nM working solution (final volume = 100 μL) in a new tube. 3 μL of 100μM oligo stock + 97 μL dH₂O = 100 μL

• Use 1.0 μL of oligo working sln. per 10 μL LCR reaction

Part 2: Prep the DNA fragments (PCR)

• Note: Final conc. in LCR rxn is 3 nM each
• Use primers with 5' phosphates to amplify the fragment(s) of interest in 50 μL Phusion polymerase PCR reactions. Use Phusion polymerase to generates fragments with blunt ends (others produce T/A overhangs).
• OPTIONAL - Digest the template DNA: Add 1 μL FastDigest DpnI and 5μL of 10x FastDigest buffer to each PCR reaction. Incubate at 37°C for 15 min.
• Purify the product with a kit of choice (e.g. Sigma PCR clean-up)
• Measure the ng/μL of the purified sample.
• Dilute the purified dsDNA to 30 fmol/μL (30 nM)
  • The volume of purified DNA (x) you will need to dilute in a final volume of 50 μL = length in bp ÷ measured ng/μL * 30 fmol/μL * 650 fg/fmol dsDNA ÷ 1,000,000 fg/ng * 50 μL final volume.
  • Formula: x μL = length in bp ÷ measured ng/μL * 0.0195 ng/μL * 50μL
• Use 1.0 μL of diluted dsDNA per 10 μL LCR reaction

Notes:

• Cameron used ~1μL of ~24 ng/μL insert (restriction digest)
• This measured ng/μL is too low for the dsDNA dilution step (x = ~90, which is greater than 50)
• Cameron used ~36.93 fmol in a 25 μL LCR = 1.47 fmol/μL (1.47 nM), whereas the recommended amount is 3.0 fmol/μL (3 nM)
• Also appears that Tm's were not optimized to 60°C for each half of the bridge oligo