Difference between revisions of "Team:JNFLS/Protocols"

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<li>Prepare the separation gel (10%). Mix in the following order:</b>
 
<li>Prepare the separation gel (10%). Mix in the following order:</b>
 
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<li>After adding TEMED and APS to the SDS-PAGE separation gel solution, the gel will polymerize quickly, so add these two reagents when ready to pour.</li>
 
<li>After adding TEMED and APS to the SDS-PAGE separation gel solution, the gel will polymerize quickly, so add these two reagents when ready to pour.</li>
 
<li>Pour gel, leaving ∼2 cm below the bottom of the comb for the stacking gel. Make sure to remove bubbles.</li>
 
<li>Pour gel, leaving ∼2 cm below the bottom of the comb for the stacking gel. Make sure to remove bubbles.</li>

Revision as of 23:34, 17 October 2018

Protocols

PCR truncation of HCVC gene

Primers:

Enzyme digestion of pcoldII vector plasmid

  1. select 1μL plasmid
  2. add 5ul green buffer
  3. add 1ul Xhol
  4. add 1ul PstI
  5. add distilled water to 20μL
  6. water bath at 37 degrees for 10 min

Ligation

Bacterial transformation

  1. Remove cells from -80°C freezer and thaw in hand
  2. Add 1-5 μl containing 1 pg-100 ng of plasmid DNA to the cell mixture. Carefully flick the tube 4-5 times to mix cells and DNA. Do not vortex
  3. Place the mixture on ice for 2 minutes. Do not mix
  4. Heat shock at exactly 42°C for exactly 30 seconds. Do not mix.
  5. Place on ice for 2 minutes. Do not mix.
  6. Pipette 250 μl of room temperature SOC into the mixture. Immediately spread 50-100 μl onto a selection plate and incubate overnight at 37-42°C. NOTE: Selection using antibiotics other than ampicillin may require some outgrowth before plating on selective media. Colonies develop faster at temperatures above 37°C, however some constructs may be unstable at elevated temperatures.

Colony PCR

Conditions：

Gel Recycling

  1. Run electrophoresis separation of the target DNA fragment
  2. Cut off the target DNA fragments, as far as possible the unwanted cut off
  3. The cut of the glue into the 1.5m | plastic centrifuge tube, said the quality of the plastic
  4. Add the same amount of Binding Buffer(XP2), that is, add 0.3m| liquid if 0.3g is weighed
  5. Heat in a 50-60 degree bath for a few minutes until all the glue is melted, stirring to mix.
  6. Put the HiBind DNA Mini Column into the 2ml collection tube
  7. Add the HiBindDNA Mini Column with less than 700ul from the DNA solution in step 5
  8. Centrifuge 60s at 12000rpm at room temperature
  9. Discard the waste liquid and recycle the collection pipe
  10. Repeat steps 7-9 until all samples are transferred to column
  11. Add 300ul Binding Buffer
  12. Centrifuge 60s at 12000rpm at room temperature
  13. Discard the waste liquid and recycle the collection pipe
  14. Add the 700ul SPW Wash Buffer
  15. Centrifuge 60s at 12000rpm at room temperature
  16. Discard the waste liquid and recycle the collection pipe once again in steps 14-16
  17. Centrifuge the empty HiBind DNA Mini Column 1 2000rmp for 2 minutes
  18. The Hibind DNA Mini Column was transferred to 1.5m| plastic centrifuge tube
  19. Add 15-30ul Elution Buffer to the center of the membrane
  20. Let sit at room temperature for 2 minutes
  21. Centrifugation for 12000rmp at room temperature for 1 minute

plasmid extraction from positive clones using an extraction kit

  1. Decant or aspirate and discard the culture media.Centrifuge at 10,000x g for 1 minute at room temperature
  2. Add 250 uL Solution I/RNase A. Vortex or pipet up and down to mix thoroughly.Complete resuspension of cell pellet is vital for obtaining good yields.
  3. Transfer suspension into a new 15 mL microcentrifuge tube.
  4. Add250 uL Solution IL Invert and gently rotate the tube several times to obtain a dear lysate. A 2-3minute incubation may be necessary.
  5. Add 350uL Solution I Immediately invert several times until a flocculent white precipitate form.
  6. Centrifuge at maximum speed (213,000 x g) for 10 minutes. A compact white pellet will form. Promptly proceed to the next step.
  7. Insert a HiBinde DNA Mini Column into a 2 mL Collection Tube.
  8. Transfer the cleared supernatant from Step 8 by CAREFULLY aspirating it into the HiBind* DNA Mini Column. Be careful not to disturb the pellet and that no cellular debris is transferred to the HiBind" DNA Mini Column.
  9. Centrifuge at maximum speed for 1 minute.
  10. Discard the filtrate and reuse the collection tube.
  11. Add 500 uL HBC Buffer
  12. centrifuge at maximum speed for 1 minute.
  13. Discard the filtrate and reuse collection tube.
  14. Add 700uL DNA Wash buffer.
  15. Centrifuge at maximum speed for 1 minute.
  16. Discard the filtrate and reuse the collection tube.
  17. Centrifuge the empty HiBind" DNA Mini Column for 2 minutes at maximum speed to dry the column matrix.
  18. Transfer the HiBind DNA Mini Column to a clean 1.5 mL microcentrifuge tube.
  19. Add 30100 uL Elution Buffer or sterile deionized water directly to the center of the column membrane.
  20. Let sit at room temperature for 1 minute.
  21. Centrifuge at maximum speed for 1 minute. Note: This represents approximately 70% of bound DNA. An optional second elution will yield any residual DNA, though at a lower concentration
  22. Store DNA at -20degrees.

Purification of recombinant protein with His tag

    1. buffer preparation:
    Lysis Buffer 1 (under native condition)
  • 0.5mM Tris-HCl
  • 0.5M NaCl
  • 5%(w/v) glycerol
  • 10mM Imidazole
  • 100mg(1mg/ml) lysozyme (Purification of 6xHis-tagged proteins from E.coli)
  • 1% Nonidet P40 (NP40 = Igepal CA-630)
  • 0.25% Tween 20 （or Triton 100）
  • 0.02% NaN3 (Optional)
  • 2 tablets of protease inhibitor cocktail (EDTA free, Recommended)
  • 200 μg(2μg/ml) RNase A (Optional) 1mg (10μg/ml) DNase1 (Optional)
  • 50 mM NaF (Optional)
  • 1mM Na3VO4 (Optional)
  • + ddH2O to 100ml, adjust pH to 8.0 using NaOH
    Lysis Buffer 2(under denature condition)
  • 50 mM Tris-Cl
  • 8 M Urea (or 6 M Gu-HCl)
  • 10mM Imidazole
  • 0.05% Tween 20
  • Adjust pH to 8.0 using NaOH
    Dialysis/Tev cleavage Buffer
  • 50 mM Tris-Cl, pH8.0
  • 100 mM NaCl (depends on solubility of protein)
  • 2.5% glycerol
  • 0.5mM EDTA
  • 0.5mM DTT or TCEP
    Buffer A：
  • 50mM Tris-HCl
  • 0.5M NaCl
  • 5% glycerol
  • 0.05% Tween 20
  • Adjust pH to 8.0 using high-concentration HCl
    Buffer B（washing buffer）：
  • li50mM Tris-Cl /li
  • 0.5M NaCl 5% glycerol
  • 0.05% Tween 20
  • 500mM imidazole
  • Adjust pH to 8.0 using high-concentration HCl
    Buffer C（imidazole gradient washing buffer）：
  • Prepare with buffer A and buffer B at different ratio: A 90ml, B 10ml
    Sample pretreatment：
  • fully suspend centrifuge-collected bacteria at the ratio wet bacteria per gram/ 4~5ml Lysis Buffer，and place overnight in -80℃ fridge
  • thaw the bacteria at 4℃ and suspend the bacteria
  • break the bacteria in two turns, which contain 5s of ultrasonic breaking, 5s of cooling for each cycle and run 10min per turn, at 400W.
  • centrifuge at 4℃, 12000rpm for 30min，collect supernatant liquid, and adjust the pH with NaOH to 8.0
  • take 1ml Ni-NTA agarose gel and place it into 15ml centrifuge tube, then centrifuge at 2000 rpm for 2 min
  • take the supernatant liquid；add 5ml Lysis Buffer, centrifuge at low speed, then take the supernatant liquid.
  • add4-5 ml bacteria lysate，and rotate at 4℃ at low speed for 1h
  • Load the chromatographic column
  • Wash the chromatographic column with buffer C to wash off protein in the column

    Improvement on purification method

    • Imp1: Add 1% N-Lauryol-Sarcosine (weak denaturant) into buffer for purification. Other procedures and reagents are the same as those shown above.
    • Imp2: Dialyze the purified protein using 3k dialysis membrane (the buffer is pbs 50% glycerol)
    • Imp3: Dilute dialyzed protein with 50 mM tris and 100mM NaCl with the proportion of 1：1

    SDS-PAGE

    1. Prepare the separation gel (10%). Mix in the following order:

    2. After adding TEMED and APS to the SDS-PAGE separation gel solution, the gel will polymerize quickly, so add these two reagents when ready to pour.
    3. Pour gel, leaving ∼2 cm below the bottom of the comb for the stacking gel. Make sure to remove bubbles.
    4. Layer the top of the gel with isopropanol. This will help to remove bubbles at the top of the gel and will also keep the polymerized gel from drying out. o In ∼30 min, the gel should be completely polymerized.
    5. Remove the isopropanol and wash out the remaining traces of isopropanol with distilled water.
    6. Prepare the stacking gel (4%). Mix in the following order:
    7. Pour stacking gel on top of the separation gel.
    8. Add combs to make wells. In ∼30 min, the stacking gel should become completely polymerized.
    9. Clamp gel into apparatus, and fill both buffer chambers with gel running buffer according to the instructions for the specific apparatus.
    10. Load samples and molecular mass protein markers into wells for separation by electrophoresis.

      Aptamer & Rolling PCR experiment

        Sequences needed

        Reagents:

        Phi29 DNA polymerase Biomics Co., LTD T4 DNA Ligase Biomics Co., LTD 10×BSA(0.05%) ：NEB Co., LTD 10×T4 DNA ligase buffer and 10×BSA (0.05%)）and dNTPs: Dalianbao Biotech Co., LTD 10×annealing buffer： 500mM NaCl，100mM Tris-HCl(PH8.0) 1mM EDTA NEB 10X phi29 DNA Polymerase Reaction Buffer：500 mM Tris-HCl 、100 mM MgCl2 、100 mM (NH4)2SO4 、40 mM DTT 、(pH 7.5 @ 25°C) TAKARA 10X T4 DNA Ligase Reaction Buffer ：500 mM Tris-HCl 、100 mM MgCl2 、10 mM ATP 、100 mM DTT 、(pH 7.5 @ 25°C)

        Examination of the reaction of designed primer, probe, and cDNA

      1. Add 2.5 µL 10 µM Aptamer Circle Probe, 2.5 µL 0.1 µM cDNA, 1uL 10×annealing buffer, 4µL ddH2O to the 10 uL reaction system，anneal at 95 °C for 10 min, then
      2. Let cool naturally. cDNA and aptamer are not added in the negative control group. Aptamer is added in the inhibition group to form competitive and complementary binding.
      3. 2.5ul annealed product (2.5uM final concentration) is taken; 1ul Reaction Buffer, 1ul 10 x T4 DNA ligase, and ddH2O 5.5ul are added in the product; the reaction is run at 22 ° C for 2 hours.
      4. 5ul product of the ligase reaction in Step 2 is taken; 10×phi29 DNA polymerase Reaction Buffer 2 ul, phi29 DNA polymerase 1 ul, BSA 0.5ul, 2.5mM dNTP 1ul, and ddH2O 10.5 ul are added; the reaction is run at 37°C for 2 hours.
      5. Take 4 ul reacted mixture，run 1%AGE，and observe whether rolling circle amplification products exist.
      6. Continue the reaction for 16 hours (overnight), take 4ul reacted mixture again, run 1%AGE, and observe the impact of reacting time on the reaction.

        Experiment of competition-based rolling circle amplification

        The annealing experiment is carried out according to the same method of experiment #1, as follows:

        Ligation，the protocol is consistent with #1

        Rolling PCR, the protocol is consistent with #1
      1. 5ul product of the reaction mentioned above is taken; 10×phi29 DNA polymerase Reaction Buffer 2 ul, phi29 DNA polymerase 1 ul, BSA 0.5ul, 2.5mM dNTP 1ul, and ddH2O 10.5 ul are added; the reaction is run at 37°C for 2 hours.
      2. Take 4 ul reacted mixture，run 1%AGE，and observe whether rolling circle amplification products exist.
      3. Rolling PCR, the protocol is consistent with #1

        Further experiment on rolling circle amplification

        20 ul system

      1. The above solution was diluted with multiple ratio of 1:5, 1:25, and 1:125, resulting in four parallel reactions of different concentrations
      2. Water bath at 37℃ for 30 minutes.
      3. Then add 2.5ul circle probe with different dilutions, and bathe at 67℃ for 30 minutes.
      4. 8ul of the reaction mixture is taken for ligation reaction.
        5. 20ul ligation reaction:

      5. 2ul of the above ligation product was used for the following rolling circle amplification reaction.

        Reference：

        [1] https://international.neb.com/protocols/2012/05/24/5-minute-transformation-protocol

        [2] Saiki R.K. et al. (1985). Science. 230, 1350-1354.

        [3] Powell, L.M. et al. (1987). Cell. 50, 831-840.

        [4] Sun, Y., Hegamyer, G. and Colburn, N. (1993). Biotechniques. 15, 372-374.

        [5] Sarkar, G., Kapelner, S. and Sommer, S.S. (1990). Nucleic Acids Res.. 18, 7465.

        [6] SDS-PAGE Gel. (2015). Cold Spring Harbor Protocols , 2015(7), pdb.rec087908. Retrieved from http://cshprotocols.cshlp.org/content/2015/7/pdb.rec087908.short

        [7] Li Shengtao. The expression and purification of the truncated HCV core protein (HCV Core125) and its antibody preparation [D]. Kunming university of technology,2012.

        [8] Wu Xianbo. Cloning, expression of a gene fragment encoding HCV core antigen and purification, antigenecity analysis of the recombinant protein [D]. First military medical university of the people's liberation army,2003.

        [9] Zhang Songbai, Zheng Liying, Hu xia, Shen Guangyu, Liu Xuewen, Shen Guoli, Yu Ruqin. Highly sensitive fluorescent aptasensor for thrombin detection based on competition triggered rolling circle amplification [J]. Chinese Journal of Analytical Chemistry,2015,43(11):1688-1694.

        [10] Zhou hui. Studies on competitive mechanism triggered signal amplification based aptasensors [D]. Hunan university,2009.

        [11] Dean F B, Nelson J R, Giesler T L, et al. Rapid amplification of plasmid and phage DNA using phi29 DNA polymerase and multiply-primed rolling circle amplification[J]. Genome research, 2001, 11(6): 1095-1099.

        [12] Shi S, Yu X, Gao Y, et al. Inhibition of hepatitis C virus production by aptamers against the core protein[J]. Journal of virology, 2014, 88(4): 1990-1999.

        [13] Banér J, Nilsson M, Mendel-Hartvig M, et al. Signal amplification of padlock probes by rolling circle replication[J]. Nucleic acids research, 1998, 26(22): 5073-5078.