Application of a novel protein biochip technology for detection and identification of rheumatoid arthritis biomarkers in synovial fluid

被引:87
作者
Uchida, T
Fukawa, A
Uchida, M
Fujita, K
Saito, K
机构
[1] Tohoku Univ, Dept Pathol, Inst Dev Aging & Canc, Sendai, Miyagi 9808575, Japan
[2] Ciphergen Biosyst Co, Kamakura, Kanagawa, Japan
[3] Hokkaido Univ, Sapporo, Hokkaido, Japan
关键词
ProteinChip system; rheumatoid arthritis; myeloid related protein 8; biomarkers;
D O I
10.1021/pr025531w
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We compared protein profiles of the synovial fluid of patients with rheumatoid arthritis and osteoarthritis by using surface-enhanced laser desorption/ionization mass spectrometry technology. With this approach, we identified a protein expressed specifically in the synovial fluid of the patients with rheumatoid arthritis. During the investigation, we found several reproducible and discriminatory biomarker candidates for distinction between rheumatoid arthritis and osteoarthritis. Among these candidates, a 10 850 Da protein peak was the clearest example of a single signal found specifically in the rheumatoid arthritis samples. This candidate was purified using a size-exclusion spin column followed by gel electrophoresis and subsequently identified by pepticle mapping and post-source decay (PSD) analysis. The results clearly indicate that the protein is myeloid-related protein 8, which was verified by the enzyme immunoassay. It is known that the myeloid-related protein 8 level in serum and synovial fluid is related to disease activity in juvenile rheumatoid arthritis. The results suggest that the ProteinChip platform is useful to detect and identify protein biomarkers expressed specifically in diseases or in some stage of diseases.
引用
收藏
页码:495 / 499
页数:5
相关论文
共 22 条
  • [1] THE CALCIUM-BINDING PROTEINS MRP8 AND MRP14 FORM A MEMBRANE-ASSOCIATED HETERODIMER IN A SUBSET OF MONOCYTES MACROPHAGES PRESENT IN ACUTE BUT ABSENT IN CHRONIC INFLAMMATORY LESIONS
    BHARDWAJ, RS
    ZOTZ, C
    ZWADLOKLARWASSER, G
    ROTH, J
    GOEBELER, M
    MAHNKE, K
    FALK, M
    MEINARDUSHAGER, G
    SORG, C
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (07) : 1891 - 1897
  • [2] Burkhardt K, 2001, J AM SOC NEPHROL, V12, P1947, DOI 10.1681/ASN.V1291947
  • [3] Cunnane Gaye, 1998, Archivum Immunologiae et Therapiae Experimentalis, V46, P1
  • [4] Transendothelial migration of 27E10+ human monocytes
    Eue, I
    Pietz, B
    Storck, J
    Klempt, M
    Sorg, C
    [J]. INTERNATIONAL IMMUNOLOGY, 2000, 12 (11) : 1593 - 1604
  • [5] Frosch M, 2000, ARTHRITIS RHEUM-US, V43, P628, DOI 10.1002/1529-0131(200003)43:3<628::AID-ANR20>3.0.CO
  • [6] 2-X
  • [7] Correlation between protein and mRNA abundance in yeast
    Gygi, SP
    Rochon, Y
    Franza, BR
    Aebersold, R
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1999, 19 (03) : 1720 - 1730
  • [8] MRP-8 AND MRP-14, 2 ABUNDANT CA-2+-BINDING PROTEINS OF NEUTROPHILS AND MONOCYTES
    HESSIAN, PA
    EDGEWORTH, J
    HOGG, N
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1993, 53 (02) : 197 - 204
  • [9] Integrated genomic and proteomic analyses of a systematically perturbed metabolic network
    Ideker, T
    Thorsson, V
    Ranish, JA
    Christmas, R
    Buhler, J
    Eng, JK
    Bumgarner, R
    Goodlett, DR
    Aebersold, R
    Hood, L
    [J]. SCIENCE, 2001, 292 (5518) : 929 - 934
  • [10] Jenkins RE, 2001, PROTEOMICS, V1, P13, DOI 10.1002/1615-9861(200101)1:1<13::AID-PROT13>3.3.CO