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在一个希腊裔家族的家族性淀粉样多神经病中存在血浆转甲状腺素蛋白(前白蛋白)变体。

Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.

作者信息

Saraiva M J, Sherman W, Goodman D S

出版信息

J Lab Clin Med. 1986 Jul;108(1):17-22.

PMID:3011930
Abstract

Human plasma transthyretin (TTR, a protein formerly called prealbumin) is known to be associated with familial amyloidotic polyneuropathy (FAP) of autosomal inheritance. A variant TTR with a methionine-for-valine substitution at position 30 has been described as the major protein component of amyloid in Portuguese and Japanese patients with FAP and in patients of Swedish ancestry with FAP. In these patients, TTR(Met30) also circulates in relatively low concentration in the plasma. TTR variants having substitutions in other positions have also been reported in a patient of Jewish origin with FAP. We now report studies on TTR from an FAP kindred of Greek ancestry. By peptide mapping analysis, plasma TTR from the propositus was compared with TTR from a Portuguese patient with FAP. TTR(Met30) was found to circulate in the blood plasma of the Greek propositus. By use of a recently developed immunoblotting technique, this variant TTR was also detected in some of the relatives of the propositus. Future studies of this mutant gene among ethnically different FAP populations might contribute to an understanding of selection and persistence of the mutation.

摘要

已知人血浆甲状腺素运载蛋白(TTR,一种以前称为前白蛋白的蛋白质)与常染色体显性遗传的家族性淀粉样多神经病(FAP)相关。在患有FAP的葡萄牙和日本患者以及具有瑞典血统的FAP患者中,已将在第30位缬氨酸被蛋氨酸取代的变异型TTR描述为淀粉样蛋白的主要蛋白质成分。在这些患者中,TTR(Met30)在血浆中的循环浓度也相对较低。在一名患有FAP的犹太裔患者中也报道了在其他位置有取代的TTR变异体。我们现在报告对来自希腊血统FAP家族的TTR的研究。通过肽图分析,将先证者的血浆TTR与一名患有FAP的葡萄牙患者的TTR进行了比较。发现TTR(Met30)在希腊先证者的血浆中循环。通过使用最近开发的免疫印迹技术,在一些先证者的亲属中也检测到了这种变异型TTR。在不同种族的FAP人群中对这种突变基因的进一步研究可能有助于理解该突变的选择和持续性。

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