Beswick H T, Harding J J
Nuffield Laboratory of Ophthalmology, University of Oxford, U.K.
Biochem J. 1987 Sep 15;246(3):761-9. doi: 10.1042/bj2460761.
There is good evidence that the non-enzymic chemical modification of proteins plays a role in the aetiology of cataract and diabetic sequelae. This paper presents new evidence that glycosylation of two major lens structural crystallins, alpha- and gamma-crystallins, by glucose 6-phosphate (G6P) induces conformational changes in the proteins. In addition the surface charge on the molecules is altered. These changes would affect protein-protein and protein-water interactions within the lens and could lead to disruption of the short-range order of the lens proteins which is essential for lens transparency. Conformational changes to lens proteins are known to occur in human cataractous lenses but their cause in vivo is not established. Cumulative chemical modification of proteins, over a period of decades, is a strong candidate as a causal agent.
有充分证据表明蛋白质的非酶化学修饰在白内障和糖尿病后遗症的病因学中起作用。本文提出了新的证据,即6-磷酸葡萄糖(G6P)对晶状体的两种主要结构晶体蛋白α-晶体蛋白和γ-晶体蛋白进行糖基化会诱导蛋白质的构象变化。此外,分子表面电荷也会改变。这些变化会影响晶状体内蛋白质-蛋白质和蛋白质-水的相互作用,并可能导致晶状体蛋白短程有序结构的破坏,而这种结构对于晶状体的透明度至关重要。已知晶状体蛋白的构象变化会发生在人类白内障晶状体中,但它们在体内的成因尚未确定。在几十年的时间里,蛋白质的累积化学修饰是一个很有可能的致病因素。