Membrane topology of bovine adrenocortical cytochrome P-450C21: structural studies by trypsin digestion in vesicle membranes.
Membrane topology of bovine adrenocortical cytochrome P-450C21: structural studies by trypsin digestion in vesicle membranes.
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牛肾上腺皮质细胞色素 P-450C21 的膜拓扑:通过胰蛋白酶消化囊泡膜进行结构研究。
DOI:
10.1021/bi00210a048
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发表时间:
1993
期刊:
影响因子:
2.9
通讯作者:
S. Takemori
中科院分区:
文献类型:
--
作者:
S. Kominami;H. Tagashira;Y. Ohta;M. Yamada;S. Kawato;S. Takemori
Purified adrenocortical microsomal P-450C21 was incorporated into vesicle membranes composed of phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine at a molar ratio of 5:3:1. Trypsinolysis of the incorporated P-450C21 resulted in the formation of 30-, 25-, and 20-kDa fragments. Similar fragment formation was observed by trypsinolysis of bovine adrenocortical microsomes with Western blotting using anti-P-450C21 IgG. In the detergent-solubilized state, trypsin cleaved P-450C21 into very small peptides. Washing of the trypsin-treated vesicles with 500 mM Na2CO3 failed to cause these fragments to separate from membranes. N-Terminal amino acid sequencing of these fragments showed that trypsin cleaved the 267 Arg-268Val and 332Arg-333Val bonds of P-450C21. The time course of fragment formation indicated that trypsin cleaved the 267Arg-268Val bond first to produce 30- and 25-kDa fragments and subsequently the 332Arg-333Val bond in the 25-kDa fragment to produce the 20-kDa fragment. Neither 21-hydroxylase activity, the reduced CO difference spectrum, nor the EPR spectrum of digested P-450C21 differed from those of undigested P-450C21. Heat treatment at 50 degrees C for 20 min did not cause any decrease in activity of digested P-450C21, when the substrate progesterone was present. This high stability toward heat treatment was not observed in the solubilized state. Rotational diffusion experiments on P-450C21 showed that the size of the molecule holding the heme was not changed significantly after digestion. On the basis of these results, P-450C21 is concluded to be deeply embedded in the vesicle membranes.
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DOI:
--
发表时间:
1989
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Yanase,T;Kagimoto,M;Suzuki,S;Hashiba,K;Simpson,ER;Waterman,MR
通讯作者:
Waterman,MR
DOI:
10.1016/s0021-9258(18)89040-8
发表时间:
1985-05
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
J. Ozols;F. S. Heinemann;E. F. Johnson
通讯作者:
J. Ozols;F. S. Heinemann;E. F. Johnson
影响因子:
5.6
作者:
POULOS, TL;FINZEL, BC;HOWARD, AJ
通讯作者:
HOWARD, AJ
DOI:
10.1073/pnas.80.21.6552
发表时间:
1983
影响因子:
11.1
作者:
Tarr,GE;Black,SD;Fujita,VS;Coon,MJ
通讯作者:
Coon,MJ
DOI:
--
发表时间:
1985-12
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
T. Poulos;Barry C. FinzelSY;Irwin C. Gunsalusll;G. Wagner;J. Kraut
通讯作者:
T. Poulos;Barry C. FinzelSY;Irwin C. Gunsalusll;G. Wagner;J. Kraut