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肝微粒体中存在的肝胆固醇生物合成抑制剂的特性研究

Characterization of an inhibitor of hepatic cholesterogenesis present in hepatic microsomes.

作者信息

Haven G T, Krzemien J R

出版信息

Prep Biochem. 1979;9(1):43-59. doi: 10.1080/00327487908061671.

Abstract

An inhibitor of hepatic cholesterol synthesis present in hepatic microsomes can be solubilized either by an acetone or an ethanol powder preparation. Other methods such as methanol and chloroform:methanol powder preparations and treatment with EDTA do not solubilize the factor. The factor appears to be proteinaceous since its activity is lost after exposure to proteolytic enzymes and heat treatment. In addition, the inhibitor does not require a phospholipid for activity. 3this inhibitor is stable for long periods (60 hrs.) at room temperature and can be isolated in good yield from liver maintained at 4 degrees C for 8 hours postmortem.

摘要

肝微粒体中存在的一种肝胆固醇合成抑制剂可通过丙酮或乙醇粉末制剂溶解。其他方法,如甲醇和氯仿:甲醇粉末制剂以及用乙二胺四乙酸(EDTA)处理,均不能溶解该因子。该因子似乎是蛋白质类的,因为其活性在暴露于蛋白水解酶和热处理后会丧失。此外,该抑制剂的活性不需要磷脂。这种抑制剂在室温下可长期(60小时)保持稳定,并且可以从死后在4摄氏度下保存8小时的肝脏中以较高产率分离得到。

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