Amphipol trapping of a functional CYP system

TY - JOUR

T1 - Amphipol trapping of a functional CYP system

AU - Laursen, Tomas

AU - Naur, Peter

AU - Møller, Birger Lindberg

PY - 2013/2

Y1 - 2013/2

N2 - In plants, some enzymes of the cytochrome P450 (CYP) superfamily are thought to organize into transient dynamic metabolons to optimize the biosynthesis of bioactive natural products. Metabolon formation may facilitate efficient turnover of labile and toxic intermediates and prevent undesired metabolic cross talk. Two CYPs, CYP79A1 and CYP71E1 involved in the synthesis of dhurrin, were used to assess the possibility to use amphipols (APols) to trap these membrane-bound enzymes in a soluble form in a detergent-free environment. APol surfactants are short polymers composed of a hydrophilic backbone randomly grafted with hydrophobic side chains. An optimal ratio of 1:2 w/w of protein to APol (A8-35) was required for trapping the single transmembrane helices of CYP79A1, CYP71E1, and the electron partner cytochrome P450 oxidoreductase (POR). CYP79A1 and POR retained their individual activity upon A8-35 trapping, whereas a direct interaction between CYP79A1 and POR was hampered, probably due to electrostatic repulsion caused by the negatively charged APol molecules. Upon substitution of POR with NADPH-ferredoxin oxidoreductase and ferredoxin as an electron donor system, the CYPs were shown to be catalytically active. The use of APol surfactants in functional and structural studies of membrane proteins is discussed.

AB - In plants, some enzymes of the cytochrome P450 (CYP) superfamily are thought to organize into transient dynamic metabolons to optimize the biosynthesis of bioactive natural products. Metabolon formation may facilitate efficient turnover of labile and toxic intermediates and prevent undesired metabolic cross talk. Two CYPs, CYP79A1 and CYP71E1 involved in the synthesis of dhurrin, were used to assess the possibility to use amphipols (APols) to trap these membrane-bound enzymes in a soluble form in a detergent-free environment. APol surfactants are short polymers composed of a hydrophilic backbone randomly grafted with hydrophobic side chains. An optimal ratio of 1:2 w/w of protein to APol (A8-35) was required for trapping the single transmembrane helices of CYP79A1, CYP71E1, and the electron partner cytochrome P450 oxidoreductase (POR). CYP79A1 and POR retained their individual activity upon A8-35 trapping, whereas a direct interaction between CYP79A1 and POR was hampered, probably due to electrostatic repulsion caused by the negatively charged APol molecules. Upon substitution of POR with NADPH-ferredoxin oxidoreductase and ferredoxin as an electron donor system, the CYPs were shown to be catalytically active. The use of APol surfactants in functional and structural studies of membrane proteins is discussed.

U2 - 10.1002/bab.1092

DO - 10.1002/bab.1092

M3 - Journal article

C2 - 23586999

SN - 0885-4513

VL - 60

SP - 119

EP - 127

JO - Biotechnology and Applied Biochemistry

JF - Biotechnology and Applied Biochemistry

IS - 1

ER -