Chloroplast protein Extraction From Arabidopsis
Protocol from Isolation of chloroplast proteins from Arabidopsis thaliana for proteome analysis. Klaas J van Wijk , Jean-Benoit Peltier, Lisa Giacomelli. Methods Mol Biol. 2007:355:43-8. doi: 10.1385/1-59745-227-0:43.
Procedure:
1. Cut the filter membrane (EMD Millipore 1 PC × 1 ROLL) into small pieces and wet them with ddH2O;
2. Collect fresh plant tissue, add to 1L of Medium I and crush with a blender;
3.Filter the crushed sample through the filter membrane and transfer to a 50 ml centrifuge tube;
4. Centrifuge at 4 ℃ 4,200g for 5 minutes;
5. Discard the supernatant and add 1 ml of Medium II+sorbitol to the precipitate to homogenize the mixture;
6. Centrifuge at 4 ℃ 4,200g for 5 minutes;
7.Lyse chloroplasts : Discard the supernatant and add 1 ml of Medium II-Sorbitol to the precipitate to mix completely;
8. BSA method/Kamas Brilliant Blue staining method to measure the chloroplast protein concentration;
9. Add 5 x Laemelli Buffer to denature at 70 ℃ for 10 minutes, and store the sample at -40 ℃ after denaturation is complete.
Solutions Required
Medium I
0.33M Sorbitol (M=182.17) 60.12g
30mM Tricine/KOH (0.5M, pH 8.4) 40ml
5 mM EDTA (0.25M, pH 8.35) 20ml
10 mM NaHCO3 (M=84.01) 20ml
Add ddH2O to 1L
Medium II+sorbitol
0.3M Sorbitol (M=182.17) 13.66g
20mM Hepes/KOH (1M, pH 7.6) 5ml
2.5 mM EDTA (0.5M, pH 8.0) 1.25ml
5 mM MgCl2 (M=203.3) 0.255g
Add ddH2O to 250ml
Medium II-sorbitol
20mM Hepes/KOH (1M, pH 7.6) 5ml
2.5 mM EDTA (0.5M, pH 8.0) 1.25ml
5 mM MgCl2 (M=203.3) 0.255g
Add ddH2O to 100ml
5×Laemelli Buffer
1 M Tris-Hcl (PH=6.8) 0.875mL
Glycerol 4.5 mL
SDS 0.5g
0.25% Bromophenol blue 0.5mL
2-ME 1.25 mL
Add ddH2O to 10mL