Antibody detection in human serum using a versatile protein chip platform constructed by applying nanoscale self-assembled architectures on gold

被引:42
作者
Pavlickova, P
Lensen, NM
Paul, H
Schaeferling, M
Giammasi, C
Kruschina, M
Du, WD
Theisen, M
Ibba, M
Ortigao, F
Kambhampati, D
机构
[1] ThermoHybaid, D-89077 Ulm, Germany
[2] Statens Serum Inst, Dept Tuberculosis Immunol, DK-2300 Copenhagen, Denmark
[3] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen, Denmark
关键词
protein chip; antibody; self-assembled monolayer; microarray; gold; Lyme borreliosis;
D O I
10.1021/pr0200036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report a novel high-throughput (HTP) protein chip platform, constructed on gold using self-assembly techniques, for conducting high quality antigen-antibody interactions. Biotinylated monolayers were used to immobilize a streptavidin surface with high packing density. This biocompatible platform was then used for detection of serum IgM antibodies. Serum samples of patients suspected to suffer from Lyme borreliosis were used to validate the protein chip platform using biotinylated peptide AAOspC8 molecules as the test probes. Various experimental parameters such as the effect of concentration of probes, targets, temperature of incubation, and their effect on the resulting signal-to-noise ratio are described in detail. Highly specific protein interaction data with a high signal-to-noise ratio were obtained with serum sample solutions as low as 1 muL/spot (1/10 diluted).
引用
收藏
页码:227 / 231
页数:5
相关论文
共 22 条
[11]   Sensitive and specific serodiagnosis of Lyme disease by enzyme-linked immunosorbent assay with a peptide based on an immunodominant conserved region of Borrelia burgdorferi VlsE [J].
Liang, FT ;
Steere, AC ;
Marques, AR ;
Johnson, BJB ;
Miller, JN ;
Philipp, MT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (12) :3990-3996
[12]  
MacBeath G, 2000, SCIENCE, V289, P1760
[13]   Analysis of the human antibody response to outer surface protein C (OspC) of Borrelia burgdorferi sensu stricto, B-garinii, and B-afzelii [J].
Mathiesen, MJ ;
Hansen, K ;
Axelsen, N ;
HalkierSorensen, L ;
Theisen, M .
MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 1996, 185 (03) :121-129
[14]   Peptide-based OspC enzyme-linked immunosorbent assay for serodiagnosis of Lyme borreliosis [J].
Mathiesen, MJ ;
Christiansen, M ;
Hansen, K ;
Holm, A ;
Åsbrink, E ;
Theisen, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (12) :3474-3479
[15]  
Mathiesen MJ, 1998, INFECT IMMUN, V66, P4073
[16]   Laboratory diagnostic techniques for patients with early Lyme disease associated with erythema migrans: A comparison of different techniques [J].
Nowakowski, J ;
Schwartz, I ;
Liveris, D ;
Wang, GQ ;
Aguero-Rosenfeld, ME ;
Girao, G ;
McKenna, D ;
Nadelman, RB ;
Cavaliere, LF ;
Wormser, GP .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (12) :2023-2027
[17]   QUANTITATIVE MONITORING OF GENE-EXPRESSION PATTERNS WITH A COMPLEMENTARY-DNA MICROARRAY [J].
SCHENA, M ;
SHALON, D ;
DAVIS, RW ;
BROWN, PO .
SCIENCE, 1995, 270 (5235) :467-470
[18]   Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes [J].
Schena, M ;
Shalon, D ;
Heller, R ;
Chai, A ;
Brown, PO ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10614-10619
[19]   A comprehensive analysis of protein-protein interactions in Saccharomyces cerevisiae [J].
Uetz, P ;
Giot, L ;
Cagney, G ;
Mansfield, TA ;
Judson, RS ;
Knight, JR ;
Lockshon, D ;
Narayan, V ;
Srinivasan, M ;
Pochart, P ;
Qureshi-Emili, A ;
Li, Y ;
Godwin, B ;
Conover, D ;
Kalbfleisch, T ;
Vijayadamodar, G ;
Yang, MJ ;
Johnston, M ;
Fields, S ;
Rothberg, JM .
NATURE, 2000, 403 (6770) :623-627
[20]   Genome-wide expression monitoring in Saccharomyces cerevisiae [J].
Wodicka, L ;
Dong, HL ;
Mittmann, M ;
Ho, MH ;
Lockhart, DJ .
NATURE BIOTECHNOLOGY, 1997, 15 (13) :1359-1367