Detection of novel truncated forms of human serum amyloid A protein in human plasma

被引:60
作者
Kiernan, UA [1 ]
Tubbs, KA [1 ]
Nedelkov, D [1 ]
Niederkofler, EE [1 ]
Nelson, RW [1 ]
机构
[1] Intrinsic Bioprobes Inc, Tempe, AZ 85281 USA
关键词
mass spectrometry; immunoassay; human plasma; serum amyloid A protein; truncation;
D O I
10.1016/S0014-5793(03)00097-8
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
Serum amyloid A protein (SAA) is a human plasma protein that has been recognized as potential biomarker of multiple ailments including myocardial infarction, inflammatory disease and amyloiosis. Presented here is the application of a novel immunoassay technique, termed mass spectrometric immunoassay for the detection and identification of SAA present in human plasma. Results demonstrate the ability to readily detect known SAA isotypes, and to identify novel truncated forms of SAA, in the plasma of healthy individuals and those suffering from acute and chronic inflammation. The approach represents a rapid and sensitive means for the routine structural characterization of known SAA isotypes and the discovery of associated post-translational modifications. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:166 / 170
页数:5
相关论文
共 25 条
[1]   A NOVEL ALLELIC VARIANT OF SERUM AMYLOID-A, SAA1-GAMMA - GENOMIC EVIDENCE, EVOLUTION, FREQUENCY, AND IMPLICATION AS A RISK FACTOR FOR REACTIVE SYSTEMIC AA-AMYLOIDOSIS [J].
BABA, S ;
MASAGO, SA ;
TAKAHASHI, T ;
KASAMA, T ;
SUGIMURA, H ;
TSUGANE, S ;
TSUTSUI, Y ;
SHIRASAWA, H .
HUMAN MOLECULAR GENETICS, 1995, 4 (06) :1083-1087
[2]   A NOVEL POLYMORPHISM OF HUMAN SERUM AMYLOID-A PROTEIN, SAA1-GAMMA, IS CHARACTERIZED BY ALANINES AT BOTH RESIDUE-52 AND RESIDUE-57 [J].
BABA, S ;
TAKAHASHI, T ;
KASAMA, T ;
FUJIE, M ;
SHIRASAWA, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 303 (02) :361-366
[3]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[4]   THE HUMAN ACUTE-PHASE SERUM AMYLOID-A GENE FAMILY - STRUCTURE, EVOLUTION AND EXPRESSION IN HEPATOMA-CELLS [J].
BETTS, JC ;
EDBROOKE, MR ;
THAKKER, RV ;
WOO, P .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1991, 34 (04) :471-482
[5]  
CABANA VG, 1989, J LIPID RES, V30, P39
[6]   Serum amyloid A in Alzheimer's disease brain is predominantly localized to myelin sheaths and axonal membrane [J].
Chung, TF ;
Sipe, JD ;
McKee, A ;
Fine, RE ;
Schreiber, BM ;
Liang, JS ;
Johnson, RJ .
AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION, 2000, 7 (02) :105-110
[7]   Amyloid precursors and amyloidosis in inflammatory arthritis [J].
Cunnane, G .
CURRENT OPINION IN RHEUMATOLOGY, 2001, 13 (01) :67-73
[8]   SERUM AMYLOID-A PROTEIN AND C-REACTIVE PROTEIN-LEVELS IN PULMONARY TUBERCULOSIS - RELATIONSHIP TO AMYLOIDOSIS [J].
DEBEER, FC ;
NEL, AE ;
GIE, RP ;
DONALD, PR ;
STRACHAN, AF .
THORAX, 1984, 39 (03) :196-200
[9]   Characterization of human serum amyloid A protein isoforms separated by two-dimensional electrophoresis by liquid chromatography electrospray ionization tandem mass spectrometry [J].
Ducret, A ;
Bruun, CF ;
Bures, EJ ;
Marhaug, G ;
Husby, G ;
Aebersold, R .
ELECTROPHORESIS, 1996, 17 (05) :866-876
[10]  
Elliott-Bryant R, 1998, SCAND J IMMUNOL, V48, P241