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脱氧核糖核酸酶I释放的雌激素受体的物理化学性质

Physical-chemical properties of the estrogen receptor released by deoxyribonuclease I.

作者信息

Geier A, Beery R, Haimsohn M, Kessler E, Lunenfeld B

出版信息

J Steroid Biochem. 1986 May;24(5):971-6. doi: 10.1016/0022-4731(86)90348-1.

Abstract

The physical-chemical properties of the nuclear estrogen receptor released by DNase I were characterized. Nuclei were isolated from MCF-7 cells previously exposed to 10-nM-[3H]estradiol. The parameters determined were: sedimentation coefficients (S) on a sucrose gradient, Stokes radii (Rs) by gel filtration on a Sephadex G-200 column and the binding ability to a DNA-cellulose column. The molecular weights (Mr) and frictional ratios (f/fo) were calculated from the S and Rs values. The properties of the receptor released by DNase I obtained from Worthington were compared to the properties of the receptor released by DNase I obtained from Sigma. Digestion with DNase I (Worthington) excised a receptor form which could be solubilized from nuclei by EDTA. This form sedimented at 5.2S with a Rs = 7.08 nm and a calculated Mr = 152.000. About 40% of this receptor form bound to a DNA-cellulose column. 0.4 M KCl dissociated this receptor form into a smaller form sedimenting at 4.2S with Rs = 4.64 nm and a calculated Mr = 80.000. The properties of the receptor solubilized by micrococcal nuclease followed by DNase I (Worthington) digestion were identical to the properties of the DNase I (Worthington) released receptor. Digestion with DNase I (Sigma) released a 3.2S receptor form, which diffused through the nuclear membrane and a 4-5S form which could be extracted from nuclei by EDTA. The 3.2S receptor had a Rs = 2.41 nm, a calculated Mr = 32.000 and less than 5% of it bound to a DNA-cellulose column. Digestion with micrococcal nuclease followed by DNase I (Sigma) solubilized a receptor form with identical properties to the 3.2S receptor. These results suggest that DNase I (Worthington) released a receptor form still associated with some molecules, probably chromatin proteins, which complexed it to DNA, while DNase I (Sigma) released the estradiol binding fragment of the receptor (meroreceptor) as a result of a proteolytic activity present in this preparation.

摘要

对脱氧核糖核酸酶I释放的核雌激素受体的物理化学性质进行了表征。从先前暴露于10 nM [3H]雌二醇的MCF-7细胞中分离细胞核。测定的参数包括:在蔗糖梯度上的沉降系数(S)、在Sephadex G-200柱上通过凝胶过滤测定的斯托克斯半径(Rs)以及与DNA纤维素柱的结合能力。根据S和Rs值计算分子量(Mr)和摩擦比(f/fo)。将从沃辛顿公司获得的脱氧核糖核酸酶I释放的受体的性质与从西格玛公司获得的脱氧核糖核酸酶I释放的受体的性质进行了比较。用脱氧核糖核酸酶I(沃辛顿公司)消化可切除一种受体形式,该形式可通过EDTA从细胞核中溶解出来。这种形式在5.2S沉降,Rs = 7.08 nm,计算出的Mr = 152,000。这种受体形式约40%与DNA纤维素柱结合。0.4 M KCl将这种受体形式解离成一种较小的形式,在4.2S沉降,Rs = 4.64 nm,计算出的Mr = 80,000。经微球菌核酸酶处理后再用脱氧核糖核酸酶I(沃辛顿公司)消化溶解的受体的性质与脱氧核糖核酸酶I(沃辛顿公司)释放的受体的性质相同。用脱氧核糖核酸酶I(西格玛公司)消化释放出一种3.2S的受体形式,它可扩散穿过核膜,还有一种4 - 5S的形式可通过EDTA从细胞核中提取出来。3.2S的受体Rs = 2.41 nm,计算出的Mr = 32,000,且不到5%与DNA纤维素柱结合。经微球菌核酸酶处理后再用脱氧核糖核酸酶I(西格玛公司)消化溶解的一种受体形式与3.2S受体具有相同的性质。这些结果表明,脱氧核糖核酸酶I(沃辛顿公司)释放出一种仍与一些分子(可能是染色质蛋白)相关的受体形式,这些分子使其与DNA结合,而脱氧核糖核酸酶I(西格玛公司)由于该制剂中存在的蛋白水解活性释放出受体的雌二醇结合片段(部分受体)。

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