Currie R A, Budziak T E, Cidlowski J A
Arch Biochem Biophys. 1983 Sep;225(2):906-15. doi: 10.1016/0003-9861(83)90105-4.
A comparison of the physicochemical properties between pyridoxal 5'-phosphate- and 0.4 M KCl-extracted nuclear glucocorticoid receptors has been made utilizing HeLa S3 cells as a source of receptor. Both pyridoxal 5'-phosphate/NaBH4-reduced and 0.4 M KCl-extracted receptors sedimented as approximately 3.5-4.5 S species in 5-20% sucrose gradients containing 0, 0.15, and 0.4 M KCl. Under low-ionic-strength buffer conditions, pyridoxal 5'-phosphate-extracted receptor elutes close to the void volume of a Sephacryl S-300 gel-exclusion column. Increasing the [KCl] of the column to 0.4 M resulted in the elution of receptor with a Stokes radius of 58 A and calculated Mr = 96,000. Nuclear receptors extracted with 0.4 M KCl also formed a large-molecular-weight complex which eluted close to the void volume of the gel-exclusion column. Increasing the [KCl] to 0.4 M had the effect of shifting this receptor form to a species which had a Stokes radius of 62 A and calculated Mr = 89,700. Ion-exchange analysis of nuclear-extracted receptors revealed that 0.4 M KCl-extracted receptors exhibited considerable charge heterogeneity, whereas pyridoxal 5'-phosphate-extracted receptors did not. Pyridoxal 5'-phosphate-extracted receptors (approximately 86%) eluted from DEAE-cellulose at a [KCl] greater than 0.15 M; approximately 14% of the receptors had little affinity for DEAE-cellulose. Pyridoxal phosphate-treated receptors had little affinity for hydroxylapatite, phosphocellulose, and DNA-cellulose. The predominant form of 0.4 M KCl-extracted nuclear receptors (approximately 78%) eluted from DEAE-cellulose between 0.05 and 0.15 M KCl, a position coincident with "activated" glucocorticoid receptors. The remaining receptor fraction (approximately 22%) eluted from DEAE-cellulose at a [KCl] greater than 0.15 M, a position coincident with "unactivated" glucocorticoid receptors.(ABSTRACT TRUNCATED AT 400 WORDS)
以HeLa S3细胞作为受体来源,对磷酸吡哆醛和0.4M KCl提取的核糖皮质激素受体的理化性质进行了比较。在含有0、0.15和0.4M KCl的5 - 20%蔗糖梯度中,磷酸吡哆醛/硼氢化钠还原提取的受体和0.4M KCl提取的受体均以约3.5 - 4.5S的形式沉降。在低离子强度缓冲条件下,磷酸吡哆醛提取的受体在Sephacryl S - 300凝胶排阻柱的空体积附近洗脱。将柱中KCl浓度提高到0.4M,导致洗脱的受体斯托克斯半径为58 Å,计算得到的分子量为96,000。用0.4M KCl提取的核受体也形成了一种大分子复合物,在凝胶排阻柱的空体积附近洗脱。将KCl浓度提高到0.4M会使这种受体形式转变为斯托克斯半径为62 Å、计算得到的分子量为89,700的物种。对核提取受体的离子交换分析表明,0.4M KCl提取的受体表现出相当大的电荷异质性,而磷酸吡哆醛提取的受体则没有。磷酸吡哆醛提取的受体(约86%)在KCl浓度大于0.15M时从DEAE - 纤维素上洗脱;约14%的受体对DEAE - 纤维素几乎没有亲和力。磷酸吡哆醛处理的受体对羟基磷灰石、磷酸纤维素和DNA - 纤维素几乎没有亲和力。0.4M KCl提取的核受体的主要形式(约78%)在0.05至0.15M KCl之间从DEAE - 纤维素上洗脱,这一位置与“活化”的糖皮质激素受体一致。其余的受体部分(约22%)在KCl浓度大于0.15M时从DEAE - 纤维素上洗脱,这一位置与“未活化”的糖皮质激素受体一致。(摘要截于400字)