Lipecky R, Kohlschein J, Gassen H G
Nucleic Acids Res. 1977 Oct;4(10):3627-42. doi: 10.1093/nar/4.10.3627.
In order to examine the nature of the complex formation between the ribosomal protein S1 and nucleic acids three methods were used: Inhibition of the reaction of n-ethyl[2.3 14C]-maleimide with S1 by the addition of oligonucleotides; adsorption of the complexes to nitrocellulose filters; and equilibrium dialysis. The complex formation is Mg2+ dependent at low salt concentrations and becomes Mg2+ independent at an ionic strength greater than 90 mM. Oligouridylates of increasing chain length reach an optimal KA of 3-3-10(7) M-1 at a chain length of n=13-14. Protein S1 contains one binding site for long chain oligouridylates, such as U12, and the standard-free-energy change on binding caused by one Pu increment is 0.41 kcal/mol, when n varies between five and fourteen. Complex formation is insensitive to the capacity of the homopolynucleotide bases to form hydrogen bonds. Homopolynuceotides, however, showing a Tm less than 250 in the buffer system used show an increased affinity for S1 compared to poly(A) and poly(C) (Tm greater than 40 degrees). The data are discussed with respect to the proposed binding of protein S1 to the 3-terminal end of the 16S RNA.
为了研究核糖体蛋白S1与核酸之间复合物形成的性质,使用了三种方法:通过添加寡核苷酸抑制N-乙基[2,3-¹⁴C]马来酰亚胺与S1的反应;将复合物吸附到硝酸纤维素滤膜上;以及平衡透析。在低盐浓度下,复合物的形成依赖于Mg²⁺,而在离子强度大于90 mM时则变得不依赖于Mg²⁺。链长增加的寡聚尿苷酸在链长n = 13 - 14时达到最佳的KA值3.3×10⁷ M⁻¹。蛋白S1含有一个用于长链寡聚尿苷酸(如U12)的结合位点,当n在5到14之间变化时,由一个嘌呤增加引起的结合时的标准自由能变化为0.41 kcal/mol。复合物的形成对同聚核苷酸碱基形成氢键的能力不敏感。然而,在所使用的缓冲系统中,熔解温度(Tm)小于25℃的同聚核苷酸与聚(A)和聚(C)(Tm大于40℃)相比,对S1表现出更高的亲和力。结合蛋白质S1与16S RNA 3'末端的拟议结合来讨论这些数据。