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IDENTIFICATION OF 2 NOVEL AMYLOID-A PROTEIN SUBSETS COEXISTING IN AN INDIVIDUAL PATIENT OF AA-AMYLOIDOSIS
被引:34
作者:
BABA, S
TAKAHASHI, T
KASAMA, T
SHIRASAWA, H
机构:
[1] UNIV TOKYO, FAC MED, DEPT BIOCHEM, BUNKYO KU, TOKYO 113, JAPAN
[2] TOKYO MED & DENT UNIV, BIOMED ANAL LAB, BUNKYO KU, TOKYO 113, JAPAN
关键词:
AMYLOID-A PROTEIN;
SERUM AMYLOID-A PROTEIN;
RHEUMATOID ARTHRITIS;
AMINO ACID SEQUENCE;
MASS SPECTROMETRY;
D O I:
10.1016/0925-4439(92)90068-X
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 SAA2alpha and the other corresponded to positions 2-76 (or 75) of known SAA1 subsets, except for position 52 or 57, where SAA1alpha has valine and alanine and SAA1beta 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., SAA1(52,57)Ala.
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页码:195 / 200
页数:6
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