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Identification of paraoxonase 3 in rat liver microsomes: purification and biochemical properties.

机译:大鼠肝微粒体中对氧磷酶3的鉴定:纯化和生化特性。

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摘要

Three paraoxonase genes (PON1, PON2 and PON3) have been described so far in mammals. Although considerable information is available regarding PON1, little is known about PON2 and PON3. PON3 has been isolated recently from rabbit serum [Draganov, Stetson, Watson, Billecke and La Du (2000) J. Biol. Chem. 275, 33435-33442] and liver [Ozols (1999) Biochem. J. 338, 265-275]. In the present study, we have identified the presence of PON3 in rat liver microsomes and a method for the purification to homogeneity is presented. PON3 has been purified 177-fold to apparent homogeneity with a final specific activity of 461 units/mg using a method consisting of seven steps: solubilization of the microsomal fraction, hydroxyapatite adsorption, chromatography on DEAE-Sepharose CL-6B, non-specific affinity chromatography on Cibacron Blue 3GA, two DEAE-cellulose steps and a final affinity chromatography on concanavalin A-Sepharose. SDS/PAGE of the final preparation indicated a single protein-staining band with an apparent molecular mass of 43 kDa. The isolated protein was identified by nanoelectrospray MS. Internal amino acid sequences of several peptides were determined and compared with those of human, rabbit and mouse PON3, showing a high similarity. Some biochemical properties of PON3 were also studied, including optimum pH, K(m) and heat and pH stability.
机译:到目前为止,已经在哺乳动物中描述了三种对氧磷酶基因(PON1,PON2和PON3)。尽管可以获得有关PON1的大量信息,但对PON2和PON3知之甚少。最近已从兔血清中分离出PON3 [Draganov,Sterson,Watson,Billecke和La Du(2000)J.化学275、33435-33442]和肝脏[Ozols(1999)Biochem。 J. 338,265-275]。在本研究中,我们已经鉴定出大鼠肝微粒体中存在PON3,并提出了纯化至均质的方法。使用以下七个步骤组成的方法,将PON3纯化177倍,达到表观同质性,最终比活性为461个单位/ mg:微粒体部分的溶解,羟基磷灰石吸附,DEAE-Sepharose CL-6B层析,非特异性亲和力Cibacron Blue 3GA色谱,两个DEAE-纤维素步骤和伴刀豆球蛋白A-Sepharose的最终亲和色谱。最终制剂的SDS / PAGE表明具有表观分子量为43kDa的单一蛋白染色带。分离的蛋白质通过纳米电喷雾MS鉴定。确定了几种肽的内部氨基酸序列,并将其与人,兔和小鼠PON3的氨基酸序列进行了比较,显示出很高的相似性。还研究了PON3的一些生化特性,包括最佳pH,K(m)以及热和pH稳定性。

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