• Dedicated affinity matrix for membrane proteins
• Highly tolerant to detergents
• Binding capacity <3?mg ml<="" li="">
• Delivered as a 50?% suspension
• Average agarose bead size: 40 μm

• Lysis Buffer
• Wash Buffer
• Elution Buffer
• Rho1D4 peptide
• Detergents
• Ultrasonic homogenizer
• Ice bath
• Refrigerated centrifuge for 50?mL tubes (min10,000 x g) and 2?mL tubes
• Refrigerated superspeed or ultracentrifuge capable of 100.000 x g
• End-over-end rotator
• 2?mL microcentrifuge tubes
• 15?mL polypropylene tube 50?mL polypropylene tube 50?mL polycarbonate high speed centrifuge tube (for ultracentrifuge)
• Micropipettor and Micropipetting tips
• Disposable gravity flow columns with capped bottom outlet, 2 ml
• ?pH meter
• UV/VIS spectrophotometer
• SDS-PAGE reagents and equipment
  Optional: Western Blot reagents and equipment

KD of Rho1D4 antibody to 9 amino acid antigen: ca 20 nM

Sample Volume for an assay: 400-500 mL E.coli culture volume or corresponding quantity.

• Rho buffer: NaH2PO4* 10 mM NaCl* 150 mM Glycerol 10?% (v/v) Protease inhibitor 1x,?pH 7.0
  Note: Add protease inhibitor directly before use. Depending on the protein, PBS at?pH 7.4 may yield better results.
• Lysis buffer: 1 x Rho buffer with 1?mg/mL Lysozyme
• EW (Equilibration and Wash) buffer: 1 x Rho buffer with appropriate detergent
• Elution buffer: 1 x Rho buffer with appropriate detergent and 200 μm Rho1D4 peptide.
  Note: Always prepare fresh. The recommended concentration of rho1D4 peptide in the elution buffer is 200 μM-1 mM. See the rho1D4 peptide Datasheet for further instructions to reconstitute the lyophilized peptide.

A. Solubilization of the membrane protein

1. Thaw the E. coli cell pellet on ice for 15?min. Optional: Freezing the cell pellet at -20?°C for 30?min prior to incubation at room temperature improves lysis by lysozyme.
2. Resuspend the cell pellet in Lysis Buffer. Use 10?mL Lysis Buffer per g cell pellet. Pour it into a 50?mL conical centrifuge tube.
3. If the solution is very viscous, add 3?units Benzonase? per mL E.coli culture volume to the lysis buffer. Alternatively or additionally, sonicate the lysate to improve cell disruption. Note: Keep the lysates on ice to prevent warming.
4. Incubate on an end-over-end shaker at 4?°C for 1 h.
5. Centrifuge the lysate for 15?min at 900 x g and 4?°C to remove cell debris. Note: The supernatant contains the cleared lysate fraction. We recommend to take aliquots of all fractions for SDS-PAGE analysis.
6. Carefully transfer the supernatant to a fresh tube. Centrifuge for 30?min at 7,000 x g and 4?°C to precipitate inclusion bodies. Tip: Analyze the resulting pellet by SDS-PAGE to assess if target protein is present in inclusion bodies. To capture these proteins, we recommend purification via His-tag under denaturing conditions, using PureCube Ni-NTA Agarose. Alternatively, optimize expression conditions to bring the target protein into the membrane fraction.
7. Carefully transfer the supernatant to a polycarbonate high-speed centrifuge tube and centrifuge at 100,000xg for 1 h at 4?°C.
8. Discard the supernatant and resuspend the pellet in 5?mL EW Buffer. Determine protein concentration and adjust the volume with EW Buffer to a concentration of 5?mg/mL. Note the adjusted volume. Note: The solution contains the total membrane protein fraction.
9. Based on the results from the detergent screen, calculate the amount of detergent needed to solubilize the protein in the adjusted volume. Add the detergent. Note: To determine optimal detergent conditions, refer to the Cube Biotech Protocol: "Screening Detergents for Optimal Solubilization and Purification of Membrane Proteins"
10. Transfer the suspension to a clean 15?mL polypropylene centrifuge tube. Incubate on an end-over-end rotator using the incubation conditions determined in the detergent screen.
11. Transfer the suspension to a polycarbonate high-speed centrifuge tube and centrifuge at 100,000 x g for 1 h at 4?°C.
12. Transfer the supernatant to a fresh 15?mL tube and use it in part B of the protocol. Note: The solution contains the solubilized membrane protein fraction. Resuspend the PureCube Rho1D4 Agarose by inverting the bottle until the suspension is homogeneous. Transfer 0.2?mL of the 50?% suspension (corresponding to 100 μL bed volume) to a 15?mL conical centrifuge tube. Allow the resin to settle by gravity and remove the supernatant.

B. Purification of the membrane protein using Rho1D4 Agarose

1. Add 1 mL EW Buffer and gently resuspend the slurry to equilibrate the resin. Allow the resin to settle by gravity and remove the supernatant. Tip: Alternatively, resin equilibration can be performed directly in the disposable gravity flow column.
2. Pipet the soluble membrane fraction onto the equilibrated PureCube Rho1D4 Agarose and incubate at 4?C overnight on an end-over-end shaker.
3. Transfer the binding suspension to a disposable gravity flow column with a capped bottom outlet. Use EW Buffer to rinse the centrifuge tube and remove resin adhered to the wall.
4. Remove the bottom cap of the column and collect the flow-through.
5. Wash the column with 0.5 mL EW Buffer. Repeat the washing step at least 3 times.
6. Elute the rho1D4-tagged protein by adding 0.2 mL Elution Buffer. Close and rotate the column for 1 h at 4°C. Remove the top and bottom cap of the column and collect the eluate.
7. Repeat step 7 at least 5 times. Collect each eluate in a separate tube and determine the protein concentration of each fraction.
8. Analyze all fractions by SDS-PAGE and Bradford assay or spectrophotometry (280 nm). Note: Do not boil membrane proteins. Instead, incubate samples at 46?C for 30 min in preparation for SDS-PAGE analysis.
9. Optional: Perform a Western Blot assay using Rho1D4 antibody.

Analyze by SDS-PAGE, Bradford Assay or spectrophotometrically.