Sakai T T, Torget R, I J, Freda C E, Cohen S S
Nucleic Acids Res. 1975 Jul;2(7):1005-22. doi: 10.1093/nar/2.7.1005.
The binding of spermidine and ethidium bromide to mixed tRNA and phenylalanine tRNA has been studied under equilibrium conditions. The numbers and classes of binding sites obtained have been compared to those found in complexes isolated by gel filtration a low ionic strength. The latter complexes contain 10-11 moles of either spermidine or ethidium per mole of tRNA; either cation is completely displaceable by the other. In ethidium complexes, the first 2-3 moles are bound in fluorescent binding sites; the remaining 7-8 molecules bind in non-fluorescent form. At least one of the binding sites for spermidine appears similar to a binding site for fluorescent ethidium. Similar results are found with E. coli formylmethionine tRNA. Spermine, in excess of 18-20 moles per mole tRNA, causes precipitation of the complex. Putrescine does not form isolable complexes with yeast tRNA and displaces ethidium less readily from preformed ethidium-tRNA complexes. Under equilibrium conditions, in the absence of Mg++, there are 16-17 moles of spermidine bound per mole of tRNA as determined by equilibrium dialysis. Of these, 2-3 bind with a Ksence of 9 mM Mg++, the total number of binding sites is decreased slightly and there appears to be only one class of sites with a Ka = 600 M(-1). Quantitatively similar results are obtained for the binding of spermidine to yeast phenylalanine tRNA. When the interaction between ethidium bromide and mixed tRNA is studied by equilibrium dialysis or spectrophotometric titration, two classes of binding sites are obtained: 2-3 molecules bind with an average Ka = 6.6 x 10(5) M(-1) and 14-15 molecules bind with an average Ka = 4.1 x 10(4) M(-1). Spermidine, spermine, and Mg++ compete effectively for both classes of ethidium sites and have the effect of reducing the apparent binding constants for ethidium. When the binding of ethidium is studied by fluorometry, there are 3-4 highly fluorescent sites per tRNA. These sites are also affected by spermidine, spermine and Mg++. Putrescine has little effect on any of the classes of binding sites. These data are consistent with those found under non-equilibrium conditions. They suggest that polyamines bind to fairly specific regions of tRNA and may be involved in the maintenance of certain structural features of tRNA.
在平衡条件下研究了亚精胺和溴化乙锭与混合tRNA及苯丙氨酸tRNA的结合情况。将所获得的结合位点的数量和类别与在低离子强度下通过凝胶过滤分离得到的复合物中的情况进行了比较。后一种复合物每摩尔tRNA含有10 - 11摩尔亚精胺或溴化乙锭;两种阳离子均可被另一种完全取代。在溴化乙锭复合物中,最初的2 - 3摩尔结合在荧光结合位点;其余7 - 8个分子以非荧光形式结合。亚精胺的至少一个结合位点似乎与荧光溴化乙锭的结合位点相似。用大肠杆菌甲酰甲硫氨酸tRNA也得到了类似结果。每摩尔tRNA中超过18 - 20摩尔的精胺会导致复合物沉淀。腐胺不能与酵母tRNA形成可分离的复合物,并且从预先形成的溴化乙锭 - tRNA复合物中取代溴化乙锭的能力较弱。在平衡条件下,通过平衡透析测定,在没有Mg++时,每摩尔tRNA结合16 - 17摩尔亚精胺。其中,2 - 3摩尔在没有9 mM Mg++的情况下结合,结合位点总数略有减少,似乎只有一类位点,其Ka = 600 M(-1)。对于亚精胺与酵母苯丙氨酸tRNA的结合,获得了定量相似的结果。当通过平衡透析或分光光度滴定研究溴化乙锭与混合tRNA的相互作用时,得到两类结合位点:2 - 3个分子以平均Ka = 6.6×10(5) M(-1)结合,14 - 15个分子以平均Ka = 4.1×10(4) M(-1)结合。亚精胺、精胺和Mg++对两类溴化乙锭位点都有有效的竞争作用,并具有降低溴化乙锭表观结合常数的效果。当通过荧光法研究溴化乙锭的结合时,每个tRNA有3 - 4个高荧光位点。这些位点也受到亚精胺, 精胺和Mg++的影响。腐胺对任何一类结合位点几乎没有影响。这些数据与在非平衡条件下得到的数据一致。它们表明多胺与tRNA的相当特定的区域结合,并且可能参与tRNA某些结构特征的维持。