Application of sector protein microarrays to clinical samples

被引:0
|
作者
Virginia Espina
Emanuel F. Petricoin
Lance A. Liotta
David Geho
机构
[1] FDA-NCI Clinical Proteomics Program,Laboratory of Pathology, Center for Cancer Research, National Cancer Institute
[2] FDA-NCI Clinical Proteomics Program,Center for Biologics Evaluation and Research, Office of Tissue, Cell and Gene Therapy, Food and Drug Administration
关键词
Protein microarray; molecular profiling; individual targeted; sector arrays; clinical analysis;
D O I
10.1385/CP:1:1:091
中图分类号
学科分类号
摘要
Many protein functions are conferred by posttranslational modifications, which allow proteins to perform specific cellular tasks. Protein microarrays enable specific detection of posttranslational modifications not attainable by gene arrays. Reverse-phase protein microarrays have been widely adopted for use with clinical biopsy specimens because they have many advantages including highly reproducible printing of cellular lysates onto array surfaces, buit-in dilution curves, and direct detection using one antibody per analyte. This results in high-sensitivity, broad dynamic range, and favorable precision. Reverse-phase arrays have been restricted to a one slide/one antibody format. Although this is suitable for analyzing treatment effects over populations of samples, it is not well suited to individual patient assessments. One means of reaching this goal is the sector array format. Through the sector array, multiple antibody probes can be multiplexed on a single slide containing replicate immobilized aliquots from one patient. Thus, on one slide, a complete set of analytes can be characterized and used to support a therapy decision. This article describes a method for constructing sector arrays and demonstrates feasibility and adequate sensitivity applied to apoptosis related pathways.
引用
收藏
页码:91 / 99
页数:8
相关论文
共 50 条
  • [21] APPLICATION OF MICRO HPLC FOR THE DETERMINATION OF METHOTREXATE IN CLINICAL-SAMPLES
    BRANDSTETEROVA, E
    CHOVANCOVA, V
    HALKO, J
    HRC-JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY, 1992, 15 (01): : 49 - 51
  • [22] Protein microarrays as a discovery tool for studying protein-protein interactions
    Korf, U
    Wiemann, S
    EXPERT REVIEW OF PROTEOMICS, 2005, 2 (01) : 13 - 26
  • [23] Peptidomics: A new approach to affinity protein microarrays
    Scrivener, E
    Barry, R
    Platt, A
    Calvert, R
    Masih, G
    Hextall, P
    Soloviev, M
    Terrett, J
    PROTEOMICS, 2003, 3 (02) : 122 - 128
  • [24] Polyshrink™ based microfluidic chips and protein microarrays
    Mandon, Celine A.
    Heyries, Kevin A.
    Blum, Loic J.
    Marquette, Christophe A.
    BIOSENSORS & BIOELECTRONICS, 2010, 26 (04) : 1218 - 1224
  • [25] DNA and protein microarrays and their contributions to proteomics and genomics
    Ehrat, M
    Kresbach, GM
    CHIMIA, 2001, 55 (1-2) : 35 - 39
  • [26] proMAD: semiquantitative densitometric measurement of protein microarrays
    Anna Jaeschke
    Hagen Eckert
    Laura J. Bray
    BMC Bioinformatics, 21
  • [27] Protein microarrays: A powerful tool to study cancer
    Sreekumar, A
    Chinnaiyan, AM
    CURRENT OPINION IN MOLECULAR THERAPEUTICS, 2002, 4 (06) : 587 - 593
  • [28] proMAD: semiquantitative densitometric measurement of protein microarrays
    Jaeschke, Anna
    Eckert, Hagen
    Bray, Laura J.
    BMC BIOINFORMATICS, 2020, 21 (01)
  • [29] Protein microarrays: Reduced autofluorescence and improved LOD
    Walter, Johanna-Gabriela
    Stahl, Frank
    Reck, Michael
    Praulich, Inka
    Nataf, Yakir
    Hollas, Markus
    Pflanz, Karl
    Melzner, Dieter
    Shoham, Yuval
    Scheper, Thomas
    ENGINEERING IN LIFE SCIENCES, 2010, 10 (02): : 103 - 108
  • [30] Exploiting fluorescence for multiplex immunoassays on protein microarrays
    Herbath, Melinda
    Papp, Krisztian
    Balogh, Andrea
    Matko, Janos
    Prechl, Jozsef
    METHODS AND APPLICATIONS IN FLUORESCENCE, 2014, 2 (03):