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GM2神经节苷脂贮积症0型婴儿和青少年型的诊断。对天然和不同合成底物的残留活性。

Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0. Residual activities toward natural and different synthetic substrates.

作者信息

Kytzia H J, Hinrichs U, Sandhoff K

出版信息

Hum Genet. 1984;67(4):414-8. doi: 10.1007/BF00291402.

Abstract

p-Nitrophenyl-6-sulfo-2-acetamido-2-deoxy-beta-D-glucopyranoside, which is known to be a specific substrate for human hexosaminidase A, has recently been used successfully for diagnosis of variants B and B1 of GM2-gangliosidosis (Fuchs et al. 1983; Kytzia et al. 1983; Li et al. 1983). However, it is hydrolyzed by hexosaminidase S as well and is therefore not suitable for detection of patients with variant 0, who reach the normal range of activity toward this substrate. Assay of ganglioside GM2 cleaving activity in fibroblast extracts in the presence of the natural GM2 activator protein reveals residual hexosaminidase A activities of less than 2% of normal controls in two infantile and up to 7.5% in two juvenile patients with variant 0.

摘要

对硝基苯基-6-磺基-2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖苷是已知的人己糖胺酶A的特异性底物,最近已成功用于诊断GM2神经节苷脂沉积症的B型和B1型变体(Fuchs等人,1983年;Kytzia等人,1983年;Li等人,1983年)。然而,它也会被己糖胺酶S水解,因此不适用于检测0型变体患者,这类患者对该底物的活性在正常范围内。在天然GM2激活蛋白存在的情况下,对成纤维细胞提取物中神经节苷脂GM2裂解活性的测定显示,两名婴儿型0型变体患者的残余己糖胺酶A活性低于正常对照的2%,两名青少年患者的残余己糖胺酶A活性高达7.5%。

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