Schütte C G, Lemm T, Glombitza G J, Sandhoff K
Kekulé-Institut für Organische Chemie und Biochemie der Universität Bonn, Germany.
Protein Sci. 1998 Apr;7(4):1039-45. doi: 10.1002/pro.5560070421.
Lysosomal degradation of ganglioside GM2 by hexosaminidase A requires the presence of a small, non-enzymatic cofactor, the GM2-activator protein (GM2AP). Lack of functional protein leads to the AB variant of GM2-gangliosidosis, a fatal lysosomal storage disease. Although its possible mode of action and functional domains have been discussed frequently in the past, no structural information about GM2AP is available so far. Here, we determine the complete disulfide bond pattern of the protein. Two of the four disulfide bonds present in the protein were open to classical determination by enzymatic cleavage and mass spectrometry. The direct localization of the remaining two bonds was impeded by the close vicinity of cysteines 136 and 138. We determined the arrangement of these disulfide bonds by MALDI-PSD analysis of disulfide linked peptides and by partial reduction, cyanylation and fragmentation in basic solution, as described recently (Wu F, Watson JT, 1997, Protein Sci 6:391-398).
己糖胺酶A对神经节苷脂GM2的溶酶体降解需要一种小的非酶辅因子,即GM2激活蛋白(GM2AP)的存在。缺乏功能性蛋白会导致GM2神经节苷脂贮积症的AB变异型,这是一种致命的溶酶体贮积病。尽管过去人们经常讨论其可能的作用方式和功能结构域,但迄今为止尚无关于GM2AP的结构信息。在此,我们确定了该蛋白完整的二硫键模式。该蛋白中存在的四个二硫键中的两个可通过酶切和质谱进行经典测定。由于半胱氨酸136和138位置相近,阻碍了其余两个二硫键的直接定位。我们通过对二硫键连接的肽段进行基质辅助激光解吸电离-碰撞诱导解离(MALDI-PSD)分析以及如最近所述(Wu F,Watson JT,1997,Protein Sci 6:391-398)在碱性溶液中进行部分还原、氰化和片段化来确定这些二硫键的排列。