Blagoĭ Iu P, Sorokin V A, Bozhko G Kh, Valeev V A
Mol Biol (Mosk). 1975 Nov-Dec;9(6):812-9.
Using an Cphi-4A spectrophotometer (USSR), denaturation of DNA containing approximately 2% residual protein has been studied in the presence of catecholamines and their precursors: epinephrine, beta-3,4-dioxyphenylalanine, norepinephrine, 3,4-dimethoxyphenylethylamine, tyrosine, and phenylalanine. All these substances, excluding phenylalanine, induce positive excessive hyperchromicity (as compared to initial DNA). The correlation between this effect and molecular structures of the substances studied has been shown to exist. An increase of DNA hyperchromicity in the presence of catecholamines has been found to result from the oxygen presence in the aromatic rings of the catecholamines molecules. It is assumed that the interaction between the negative O-atoms in catecholamines and bivalent metal cations in the nucleoprotein complex weakens the DNA-protein binding. This leads to an additional disorientation due to the heat of nucleic acid bases, which were previously bound by the residual protein.
使用一台Cphi - 4A分光光度计(苏联),在儿茶酚胺及其前体存在的情况下,研究了含有约2%残留蛋白质的DNA的变性情况,这些儿茶酚胺及其前体包括:肾上腺素、β - 3,4 - 二羟基苯丙氨酸、去甲肾上腺素、3,4 - 二甲氧基苯乙胺、酪氨酸和苯丙氨酸。除苯丙氨酸外,所有这些物质都会诱导正向过度增色效应(与初始DNA相比)。研究表明,这种效应与所研究物质的分子结构之间存在相关性。已发现儿茶酚胺存在时DNA增色效应的增加是由于儿茶酚胺分子芳香环中存在氧。据推测,儿茶酚胺中的负氧原子与核蛋白复合物中的二价金属阳离子之间的相互作用会削弱DNA - 蛋白质的结合。这会由于先前被残留蛋白质结合的核酸碱基的热而导致额外的解取向。