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. 2010 Jan 29;19(4):731–741. doi: 10.1002/pro.349

Table II.

Crystallization Conditions

Protein buffer [Protein] (mg/mL) Crystallization conditions Ratio of protein: precipitant in crystallization drop Cryo-protectant
PDLIM1 50 mM Hepes pH 7.4, 500 mM NaCl, 0.5 mM TCEP 63 40% PEG 300, 0.2M calcium acetate, 0.1M cacodylate pH 6.5 1:2 None
PDLIM2 50 mM Hepes pH 7.4, 500 mM NaCl, 0.5 mM TCEP 12 30% mPEG 2000, 0.2M (NH4)2SO4, 0.1M acetate pH 4.6 1:2 30% Glycerol
PDLIM4 50 mM Hepes pH 7.4, 500 mM NaCl, 0.5 mM TCEP 6 20% PEG 10000, 0.2M MgCl2, 0.1M Tris pH 8.5 2:1 15% PEG400
PDLIM5 25 mM Hepes pH 7.4, 150 mM NaCl, 0.5 mM TCEP 13 30% PEG 4000, 0.2M MgCl2, 0.1M Tris pH 8.5 2:1 20% Ethylene glycol
PDLIM7 50 mM Hepes pH 7.4, 500 mM NaCl, 0.5 mM TCEP 38 20% PEG 4000, 0.1M Hepes pH 7.5, 10% isopropanol 1:2 20% Ethylene glycol
GRASP 50 mM Hepes pH 7.4, 500 mM NaCl, 0.5 mM TCEP 50 1.26M NaH2PO4, 0.14M K2HPO4 1:1 30% Glycerol
MAST4 25 mM Hepes pH 7.5, 150 mM NaCl, 0.5 mM TCEP 17 0.75M NaH2PO4, 0.91M K2HPO4 2:1 25% Ethylene glycol