Schleich T, Wickstrom E, Twombly K, Schmidt B, Tyson R W
Biochemistry. 1980 Sep 16;19(19):4486-92. doi: 10.1021/bi00560a016.
The circular dichroic spectral features of (A)10-20, (C)10-20, A8UGU6, poly(A), and poly(C), at both neutral and acidic pH values and in the presence and absence of Mg2+, are significantly altered by Escherichia coli initiation factor 3 (IF3), implying the occurrence of protein-induced changes in nucleic acid secondary structure. Similarly, the circular dichroic spectral characteristics of helical poly(U), poly-(A)-poly(U), and poly(I)-poly(C) are modified by IF3. However, no structural perturbation of poly(A)-poly(U) occurs in the absence of Mg2+ by IF3. The oligonucleotides (A)10-20 and (C)10-20 at both pH 7.5 and 5.5 titrate to end point of 26 +/- 4 nucleotide residues per IF3 [except (C) 10-20 at pH 5.5 which titrates to 17 +/- 1 nucleotide residues per IF3], whereas the hairpin A8UGU6 under similar conditions at neutral pH and in the presence of Mg2+ titrates to an end point of 56 +/- 3 nucleotide residues per IF3, thereby suggesting the presence of multiple binding sites on the protein. By contrast, poly(A) and poly(C) at neutral pH and in the absence of Mg2+ titrate to an end point of 13 +/- 1 nucleotide residues per IF3. The occurrence of significant light-scattering artifacts precluded a determination of the end point stoichiometry in most other cases. The circular dichroic spectra of E. coli tRNA, MS2 RNA, phiX174 DNA, and sonicated calf thymus DNA were unaffected by IF3 at physiological concentrations. Addition of an equimolar mixture of IF3 and ribosomal protein S1 titrates the circular dichroism of poly(C) at acid pH as did S1 alone. However, addition of IF3 to mixture of poly(A) and S1 at neutral pH did not result in significant titration of the optical activity until IF3 was in excess over S1, even though filter binding assays indicate normal IF3 binding to the polynucleotide. The possible relation of these observations to the biological function of IF3 is briefly considered.
在中性和酸性pH值条件下,以及存在和不存在Mg2+的情况下,大肠杆菌起始因子3(IF3)会显著改变(A)10 - 20、(C)10 - 20、A8UGU6、聚腺苷酸(poly(A))和聚胞苷酸(poly(C))的圆二色光谱特征,这意味着蛋白质诱导了核酸二级结构的变化。同样,IF3会改变螺旋状聚尿苷酸(poly(U))、聚腺苷酸 - 聚尿苷酸(poly(A)-poly(U))和聚肌苷酸 - 聚胞苷酸(poly(I)-poly(C))的圆二色光谱特征。然而,在不存在Mg2+的情况下,IF3不会对聚腺苷酸 - 聚尿苷酸造成结构扰动。在pH 7.5和5.5时,寡核苷酸(A)10 - 20和(C)10 - 20滴定至每个IF3对应26±4个核苷酸残基的终点[pH 5.5时的(C)10 - 20除外,其滴定至每个IF3对应17±1个核苷酸残基],而在中性pH且存在Mg +的类似条件下,发夹结构A8UGU6滴定至每个IF3对应56±3个核苷酸残基的终点,这表明该蛋白质上存在多个结合位点。相比之下,在中性pH且不存在Mg2+的情况下,聚腺苷酸和聚胞苷酸滴定至每个IF3对应13±1个核苷酸残基的终点。在大多数其他情况下,显著的光散射伪像使得无法确定终点化学计量比。在生理浓度下,IF3不会影响大肠杆菌转运RNA(tRNA)、MS2 RNA、φX17 DNA和超声处理的小牛胸腺DNA的圆二色光谱。在酸性pH条件下,加入等摩尔的IF3和核糖体蛋白S1混合物,对聚胞苷酸圆二色性的滴定效果与单独加入S1相同。然而,在中性pH条件下,向聚腺苷酸和S1的混合物中加入IF3,直到IF3过量于S1时,才会导致光学活性的显著滴定,尽管滤膜结合试验表明IF3能正常结合到多核苷酸上。本文简要探讨了这些观察结果与IF3生物学功能之间可能的关系。