Draper D E, von Hippel P H
Proc Natl Acad Sci U S A. 1979 Mar;76(3):1040-4. doi: 10.1073/pnas.76.3.1040.
The binding affinity of Escherichia coli ribosomal protein S1 for 30S ribosomal particles has been determined by a sucrose gradient band sedimentation technique; the association constant (K) for the binding of one S1 protein per active 30S ribosomal subunit is approximately 2 X 10(8) M-1. The involvement of the two polynucleotide binding sites of S1 protein (site I binding single-stranded DNA or RNA, and site II binding single-stranded RNA only) in the S1--ribosomal interaction have been examined by competition experiments with polynucleotides of known affinity for the two sites. We find that site I does not contribute to the interaction; site II binding appears to provide a major part of the binding free energy, presumably by interaction of S1 with the 16S rRNA of the 30S particle. The remaining binding free energy is probably derived from the interaction of S1 protein with other proteins of the 30S subunit. The affinity of S1 for 70S ribosomes is about the same as that for the 30S subunit; the affinity of S1 for 50S subunits is much less. Binding affinities and stoichiometries of S1 protein with "inactive" 30S ribosomal subunits have also been examined.
利用蔗糖梯度带沉降技术测定了大肠杆菌核糖体蛋白S1与30S核糖体颗粒的结合亲和力;每个活性30S核糖体亚基结合一个S1蛋白的缔合常数(K)约为2×10⁸ M⁻¹。通过与对这两个位点具有已知亲和力的多核苷酸进行竞争实验,研究了S1蛋白的两个多核苷酸结合位点(位点I结合单链DNA或RNA,位点II仅结合单链RNA)在S1与核糖体相互作用中的作用。我们发现位点I对这种相互作用没有贡献;位点II的结合似乎提供了大部分结合自由能,大概是通过S1与30S颗粒的16S rRNA相互作用实现的。其余的结合自由能可能来自S1蛋白与30S亚基其他蛋白质的相互作用。S1对70S核糖体的亲和力与对30S亚基的亲和力大致相同;S1对50S亚基的亲和力要小得多。还研究了S1蛋白与“无活性”30S核糖体亚基的结合亲和力和化学计量关系。