A new two-color Fab labeling method for autoantigen protein microarrays

被引:0
|
作者
Michael G Kattah
Golnaz R Alemi
Donna L Thibault
Imelda Balboni
Paul J Utz
机构
[1] Stanford University School of Medicine,Department of Medicine, Division of Immunology and Rheumatology
[2] Stanford University School of Medicine,Department of Pediatrics, Division of Rheumatology
来源
Nature Methods | 2006年 / 3卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Antigen microarrays hold great promise for profiling the humoral immune response in the settings of autoimmunity, allergy and cancer. This approach involves immobilizing antigens on a slide surface and then exposing the array to biological fluids containing immunoglobulins. Although these arrays have proven extremely useful as research tools, they suffer from several sources of variability. To address these issues, we have developed a new two-color Fab labeling method that allows two samples to be applied simultaneously to the same array. This straightforward labeling approach improves reproducibility and reliably detects changes in autoantibody concentrations. Using this technique we profiled serum from a mouse model of systemic lupus erythematosus (SLE) and detected both expected and previously unrecognized reactivities. The improved labeling and detection method described here overcomes several problems that have hindered antigen microarrays and should facilitate translation to the clinical setting.
引用
收藏
页码:745 / 751
页数:6
相关论文
共 50 条
  • [1] A new two-color Fab labeling method for autoantigen protein microarrays
    Kattah, Michael G.
    Alemi, Golnaz R.
    Thibault, Donna L.
    Balboni, Imelda
    Utz, Paul J.
    [J]. NATURE METHODS, 2006, 3 (09) : 745 - 751
  • [2] A novel two-color Fab labeling method for autoantigen protein microarrays.
    Kattah, Michael
    Alemi, Golnaz
    Thibault, Donna
    Utz, Paul
    [J]. CLINICAL IMMUNOLOGY, 2006, 119 : S150 - S150
  • [3] Two-color labeling of temporally defined protein populations in mammalian cells
    Beatty, Kimberly E.
    Tirrell, David A.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (22) : 5995 - 5999
  • [4] Evaluation of experimental designs for two-color cDNA microarrays
    Yang, CW
    Hsiao, CF
    Chou, CK
    [J]. JOURNAL OF COMPUTATIONAL BIOLOGY, 2005, 12 (09) : 1202 - 1220
  • [5] Variance-stabilizing transformations for two-color microarrays
    Durbin, BP
    Rocke, DM
    [J]. BIOINFORMATICS, 2004, 20 (05) : 660 - U190
  • [6] Extended analysis of benchmark datasets for Agilent two-color microarrays
    Kathleen F Kerr
    [J]. BMC Bioinformatics, 8
  • [7] Extended analysis of benchmark datasets for Agilent two-color microarrays
    Kerr, Kathleen F.
    [J]. BMC BIOINFORMATICS, 2007, 8 (1)
  • [8] Biosynthetic Labeling and Two-Color Imaging of Phospholipids in Cells
    Jao, Cindy Y.
    Roth, Mary
    Welti, Ruth
    Salic, Adrian
    [J]. CHEMBIOCHEM, 2015, 16 (03) : 472 - 476
  • [9] Hybridization as an alternative experiment design to dye swap for two-color microarrays
    Fang, Hong
    Fan, Xiaohui
    Guo, Lei
    Shi, Leming
    Perkins, Roger
    Ge, Weigong
    Dragan, Yvonne P.
    Tong, Weida
    [J]. OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY, 2007, 11 (01) : 14 - 24
  • [10] Site-Specific Two-Color Protein Labeling for FRET Studies Using Split Inteins
    Yang, Jin-Yi
    Yang, Wei Yuan
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (33) : 11644 - +