Di Matteo G, Durand P, Gatti R, Maresca A, Orfeo M, Urbano F, Romeo G
Biochim Biophys Acta. 1976 Apr 8;429(2):538-45. doi: 10.1016/0005-2744(76)90301-6.
Four major forms of alpha-fucosidase (EC 3.2.1.51) activity were separated by isoelectrofocusing from sera of normal control individuals. All forms shifted towards less acidic pI values after neuraminidase treatment. In two patients affected with fucosidosis, only a single major acidic peak was observed and this was affected to a lesser degree by neuraminidase treatment. The kinetics of heat inactivation of the residual activity found in these two patients showed two decay rates while the controls showed only one rate. These data are considered in relation to the hypothesis of the existence of interconvertible thermolabile and thermostable forms of the enzyme which has been discussed in the preceeding paper. The residual alpha-fucosidase found in patients could be structurally altered so that its ability to form the thermostable higher molecular weight aggregates is impaired.
通过等电聚焦从正常对照个体的血清中分离出四种主要形式的α-岩藻糖苷酶(EC 3.2.1.51)活性。经神经氨酸酶处理后,所有形式均向酸性较弱的pI值移动。在两名患有岩藻糖苷贮积症的患者中,仅观察到一个单一的主要酸性峰,并且该峰受神经氨酸酶处理的影响较小。这两名患者中残留活性的热失活动力学显示出两种衰减速率,而对照仅显示一种速率。结合前文讨论的关于该酶存在可相互转化的热不稳定和热稳定形式的假说对这些数据进行了考量。患者体内发现的残留α-岩藻糖苷酶可能在结构上发生了改变,从而损害了其形成热稳定的高分子量聚集体的能力。