ZOBEL C R, BEER M
J Biophys Biochem Cytol. 1961 Jul;10(3):335-46. doi: 10.1083/jcb.10.3.335.
Chemical studies have been carried out on the interaction of DNA with uranyl salts. The effect of variations in pH, salt concentration, and structural integrity of the DNA on the stoichiometry of the salt-substrate complex have been investigated. At pH 3.5 DNA interacts with uranyl ions in low concentration yielding a substrate metal ion complex with a UO(2) (++)/P mole ratio of about (1/2) and having a large association constant. At low pH's (about 2.3) the mole ratio decreases to about (1/3). Destruction of the structural integrity of the DNA by heating in HCHO solutions leads to a similar drop in the amount of metal ion bound. Raising the pH above 3.5 leads to an apparent increase in binding as does increasing the concentration of the salt solution. This additional binding has a lower association constant. Under similar conditions DNA binds about seven times more uranyl ion than bovine serum albumin, indicating useful selectivity in staining for electron microscopy.
已经对DNA与铀酰盐的相互作用进行了化学研究。研究了pH值、盐浓度和DNA结构完整性的变化对盐-底物复合物化学计量的影响。在pH 3.5时,DNA与低浓度的铀酰离子相互作用,产生一种底物-金属离子复合物,其UO(2) (++)/P摩尔比约为(1/2),且具有较大的缔合常数。在低pH值(约2.3)时,摩尔比降至约(1/3)。在HCHO溶液中加热破坏DNA的结构完整性会导致结合的金属离子量出现类似下降。将pH值提高到3.5以上会导致结合明显增加,增加盐溶液浓度时也是如此。这种额外的结合具有较低的缔合常数。在相似条件下,DNA结合的铀酰离子比牛血清白蛋白多约7倍,这表明在电子显微镜染色中具有有用的选择性。