Manchester K L
Biochim Biophys Acta. 1984 Apr 5;781(3):279-85. doi: 10.1016/0167-4781(84)90094-0.
The sedimentation characteristics on sucrose gradients of derived 40-S subunits from rat liver depend on the ionic conditions used in their preparation. Following the procedure of Wettenhall, R.E.H., Wool, I.G. and Sherton, C.C. (Biochemistry 12 (1973) 2403-2411) in which 12.5 mM Mg2+ is present throughout the preparation of the subunits, sucrose gradients of the 40-S fraction show two peaks consistent with the presence of a mixed and non-interchanging population of monomers and dimers. By contrast, when ribosomes and subunits are prepared in 2 mM Mg2+ it is shown here that 40-S subunits sediment as a single peak at a rate intermediate between that of monomers and dimers as established by prior fixation with glutaraldehyde or formaldehyde - a phenomenon observed by Spirin, A.S., Belitsina, N.V. and Lishnevskaya, E.B. (FEBS Lett. 24 (1972) 219-224) for the Escherichia coli 30-S--50-S couple but not previously shown for subunits of eukaryotic origin. Under conditions of low [Mg2+] it is suggested that the subunits are of a uniform population capable of dimerization and that equilibrium can continue during sedimentation. In the present experiments it was not possible to find tRNA in 40-S subunits as shown by Wettenhall et al. By fixation before sedimentation the relative proportions of monomers and dimers of 40 S incubated under a variety of conditions was determined. Warming from 0 to 37 degrees C increased the proportion of monomers markedly, but variation of [Mg2+] had little effect. Incubation with albumin or tRNA or spermine also had little effect, but addition of ribosomal salt-wash increased the proportion of monomers. It seems most likely that many of the 40-S subunits prepared in 12.5 mM Mg2+ have initiation factors or other proteins bound to them which prevent dimerization, but that subunits prepared at any stage with buffer containing only 2 mM Mg2+ have lost these proteins and therefore are able to dimerize to a degree depending on concentration. Different relative proportions of monomers and dimers were observed depending on whether glutaraldehyde or formaldehyde was used as fixative. Reasons are suggested for believing that formaldehyde is to be preferred to glutaraldehyde for fixation in experiments of this nature.
从大鼠肝脏中提取的40-S亚基在蔗糖梯度中的沉降特性取决于其制备过程中所使用的离子条件。按照韦滕霍尔、R.E.H.、伍尔、I.G.和谢尔顿、C.C.(《生物化学》12卷(1973年)2403 - 2411页)的方法,在整个亚基制备过程中存在12.5 mM的Mg2+,40-S组分的蔗糖梯度显示出两个峰,这与单体和二聚体的混合且不相互交换的群体的存在一致。相比之下,当核糖体和亚基在2 mM Mg2+中制备时,本文表明40-S亚基以单峰形式沉降,沉降速率介于用戊二醛或甲醛预先固定所确定的单体和二聚体的沉降速率之间——这一现象曾被斯皮林、A.S.、贝利齐娜、N.V.和利什涅夫斯卡娅、E.B.(《欧洲生物化学学会联合会快报》24卷(1972年)219 - 224页)观察到适用于大肠杆菌30-S - 50-S对,但此前未在真核生物来源的亚基中显示。在低[Mg2+]条件下,表明亚基是能够二聚化的均匀群体,并且在沉降过程中平衡可以持续。在本实验中,如韦滕霍尔等人所示,在40-S亚基中未能找到tRNA。通过在沉降前固定,确定了在各种条件下孵育的40 S单体和二聚体的相对比例。从0℃升温至37℃显著增加了单体的比例,但[Mg2+]的变化影响很小。与白蛋白、tRNA或精胺一起孵育也影响很小,但添加核糖体盐洗增加了单体的比例。看起来最有可能的是,在12.5 mM Mg2+中制备的许多40-S亚基都结合有起始因子或其他蛋白质,这些蛋白质阻止了二聚化,但在任何阶段用仅含2 mM Mg2+的缓冲液制备的亚基已经失去了这些蛋白质,因此能够根据浓度进行一定程度的二聚化。根据使用戊二醛还是甲醛作为固定剂,观察到了单体和二聚体的不同相对比例。提出了一些理由,认为在这种性质的实验中,甲醛比戊二醛更适合用于固定。