Baba S, Takahashi T, Kasama T, Shirasawa H
Second Department of Pathology, Hamamatsu University School of Medicine, Shizuoka, Japan.
Biochim Biophys Acta. 1992 Dec 10;1180(2):195-200. doi: 10.1016/0925-4439(92)90068-x.
Amyloid A protein (AA), the major fibril protein in AA-amyloidosis, is an N-terminal cleavage product of the precursor protein, serum amyloid A (SAA). Using mass spectrometry and amino-acid sequencing, we identified and characterized two novel AA protein subsets co-deposited as amyloid fibrils in an patient having AA-amyloidosis associated with rheumatoid arthritis. One of the AA proteins corresponded to positions 2-76 (or 75) of SAA2 alpha and the other corresponded to positions 2-76 (or 75) of known SAA1 subsets, except for position 52 or 57, where SAA1 alpha has valine and alanine and SAA1 beta has alanine and valine in position 52 and 57, respectively, whereas the AA protein had alanine at the both positions. Our findings (1), demonstrate that not only one but two SAA subsets could be deposited together as an AA-amyloid in a single individual and (2), support the existence of a novel SAA1 allotype, i.e., SAA152,57Ala.
淀粉样蛋白A(AA)是AA型淀粉样变性中的主要纤维蛋白,是前体蛋白血清淀粉样蛋白A(SAA)的N端裂解产物。我们使用质谱和氨基酸测序,在一名患有类风湿性关节炎相关AA型淀粉样变性的患者中,鉴定并表征了两个作为淀粉样纤维共同沉积的新型AA蛋白亚群。其中一种AA蛋白对应于SAA2α的第2至76(或75)位,另一种对应于已知SAA1亚群的第2至76(或75)位,但第52或57位除外,在该位置SAA1α有缬氨酸和丙氨酸,SAA1β在第52和57位分别有丙氨酸和缬氨酸,而该AA蛋白在这两个位置均为丙氨酸。我们的研究结果(1)表明,在单个个体中,不仅一个而且两个SAA亚群可以作为AA淀粉样蛋白共同沉积,并且(2)支持存在一种新型SAA1同种异型,即SAA152,57Ala。