DENV2 NS2B-NS3 protease co-expression construct small scale expression and purification protocol

Corrected ELN mistake

Corrected guideline construct name mistake

CV - column volume, total volume of resin in a column

IMAC - immobilised metal affinity chromatography

FT - flow through

DVNS2B3 - DENV2 NS2B-NS3 protease

DVNS2B3 N-terminal His-GST tagged co-expression construct was inoculated from its BL21(DE3)-RR glycerol stock.

Scrape off some of the glycerol stock with a sterile loop and use this to inoculate a 50 mL falcon tube containing 10mL of LB supplemented with 50 kanamycin. Grow the starter culture at 37°C 4h 0m 0s with 200 rpm shaking.

Use 10mL starter culture to inoculate every 1L Sample(see Materials) supplemented with 50 kanamycin in a baffled flask. 200rpm

When the OD₆₀₀ approximately 1.8, add 1mM IPTG. Lower the temperature and shaker speed to 180rpm. Incubate overnight.

Harvest the cell by centrifugation at 4000x g,4°C. Discard supernatant and store pellet by freezing at -80°C .

Lyse cell pellet

Thaw and resuspend the pellet in ~7mL of lysis buffer per g of pellet. Stir gently with magnetic stir bar at Room temperature for 0h 30m 0s to allow lysozyme and bezonase to start breaking down

cell components.

Lyse by sonication 0h 0m 4s 0h 0m 12s for a total 'on' time of 0h 7m 0s at 50% amplitude to fully rupture the cells. Ensure pellet is °C during sonication to prevent overheating.

Centrifuge the lysed cells for 38000x g,4°C to remove insoluble cell debris, and collect supernatant in a bottle 4°C

Perform IMAC to extract target protein from the lysed cell mixture

Dispense 3mL Nickle affinity resin Ni Sepharose 6 FF - Cytiva into a gravity flow column. Equilibrate resin by first rinsing with ~ 10 distilled water, then ~ 10 binding buffer to remove the storage solution.

Resuspend the equilibrated resin with some binding buffer and add to the supernatant bottle. Incubate the resin with the supernatant for 0h 30m 0s while rotating or otherwise mixing gently at 4°C

Load the resin/supernatant mix back onto the gravity flow column, retaining the FT separately for SDS-PAGE analysis.

Wash the column with 10 of base buffer, followed by 10 of wash buffer 1 and 2. Allow wash buffer to pass through completely between washes. This is to remove non-specific, weak binding of contaminant proteins from the resin for a cleaner elution.

Collect washes separately for SDS-PAGE analysis.

Elute the protein with 2.5 of elution buffer.

Repeat step 8.5 one more time, collecting a total of 2 separate elution fractions. This is to ensure maximum retrieval of protein from the resin.

Measure the total protein concentration of the elutions by Nanodrop. Although still a mixture, A280 value can give an estimate of the protein content, which will determine how much protease need to be added to remove the affinity tag.

For example, E1 = 18.28 mg/mL, E2 = 13.02 mg/mL at 1 A280 unit = 1 mg/mL

Wash used IMAC resin with 10CV of base buffer, and leave in the column submerged in a small amount of base buffer such that the resin is kept moist.

This washed IMAC resin will later be reused for reverse IMAC (rIMAC)

Run SDS-PAGE of all samples from total lysis supernatant to final elution. Stain gel with protein staining solution Coomasssie Blue and determine which fractions contain the target protein by finding the band corresponding to the target molecular weight.

Elution de-salting, tag cleavage and reverse IMAC

Pool and desalt the two elutions using HiPrep 26/10 deasalting columns, run on AKTA pure at the maximum flow rate of 10mL/min.

For tag removal, His-TEV was added in 1:100 ratio to the total protein content of the desalted sample, as determined by nanodrop. The mixture was left in the cold room at 4°C

In morning, pour the cleavage mixture over the washed resin three times and collect final FT.

Wash rIMAC resin with 2wash buffer 1 and 2 to remove any target protein still bound to the resin.

Take samples of the FT and wash, characterise content by SDS-PAGE

(Optional) elute rIMAC resin with 2 elution buffer to confirm if the protein shows non-specific binding to the resin used.

Purify sample further by size exclusion chromatography .

Using 10,000 MWCO spin concentrators, concentrate the rIMAC step containing fractions of the target protein to a final volume of under 5mL .

Remove any solid aggregates from the sample by centrifugation at 17200x g,4°C , then immediately draw up the supernatant with a 5mL syringe and a blunt-tip fill needle, taking care not to disturb the pellet.

Using the AKTA Pure system:

Inject the sample onto a 5mL sample loop.

Run the sample down HiLoad 16/60 Superdex 75 pg gel filtration column at 1mL/min in gel filtration buffer, collecting 1mL aliquots.

From the chromatogram, fraction F9-H8 analyse by SDS-PAGE.

Take the fractions that contain the target protein, which in this case are fraction E10-F4. Concentrate the final sample in Vivaspin 500 10kda MWCO centrifugal concentrator until the concentration reaches >23mg/mL or 1millimolar (mM) .

Take 1µL of the final sample for SDS-PAGE, and another for mass spectroscopy (MS).

Aliquot into appropriate volumes for future usage to minimise freeze/thaw cycles. Flash-freeze in liquid nitrogen, and store at -80°C until required.