Double chip protein arrays using recombinant single-chain Fv antibody fragments

被引:12
作者
Gilbert, L
Schiffmann, S
Rubenwolf, S
Jensen, K
Mail, T
Albrecht, C
Lankenau, A
Beste, G
Blank, K
Gaub, HE
Clausen-Schaumann, H
机构
[1] Nanotype, Grafelfing, Germany
[2] LMV, Lehrstuhl Angew Phys, Munich, Germany
[3] LMV, Ctr NanoSci, Munich, Germany
关键词
multiplexing; protein array; recombinant antibody; sandwich immunoassay;
D O I
10.1002/pmic.200300736
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein arrays permit the parallel analysis of many different markers in a small sample volume. However, the problem of cross-reactivity limits the degree of multiplexing in parallel sandwich immunoassays (using monoclonal antibodies (mAbs)), meaning antibodies must be pre-screened in order to reduce false positives. In contrast, we use a second chip surface for the local application of detection antibodies, thereby efficiently eliminating antibody cross-reactions. Here, we illustrate the potential advantages of using single-chain Fv fragments rather than mAbs as capture and detection molecules with this double chip technology.
引用
收藏
页码:1417 / 1420
页数:4
相关论文
共 13 条
[1]   DNA:: A programmable force sensor [J].
Albrecht, C ;
Blank, K ;
Lalic-Mülthaler, M ;
Hirler, S ;
Mai, T ;
Gilbert, I ;
Schiffmann, S ;
Bayer, T ;
Clausen-Schaumann, H ;
Gaub, HE .
SCIENCE, 2003, 301 (5631) :367-370
[2]   A force-based protein biochip [J].
Blank, K ;
Mai, T ;
Gilbert, I ;
Schiffmann, S ;
Rankl, J ;
Zivin, R ;
Tackney, C ;
Nicolaus, T ;
Spinnler, K ;
Oesterhelt, F ;
Benoit, M ;
Clausen-Schaumann, H ;
Gaub, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11356-11360
[3]   Antibodies in diagnostics - from immunoassays to protein chips [J].
Borrebaeck, CAK .
IMMUNOLOGY TODAY, 2000, 21 (08) :379-382
[4]  
Härmä H, 2000, CLIN CHEM, V46, P1755
[5]   Natural and designer binding sites made by phage display technology [J].
Hoogenboom, HR ;
Chames, P .
IMMUNOLOGY TODAY, 2000, 21 (08) :371-378
[6]   Single-chain Fv fusion proteins suitable as coating and detecting reagents in a double antibody sandwich enzyme-linked immunosorbent assay [J].
Kerschbaumer, RJ ;
Hirschl, S ;
Kaufmann, A ;
Ibl, M ;
Koenig, R ;
Himmler, G .
ANALYTICAL BIOCHEMISTRY, 1997, 249 (02) :219-227
[7]   Use of an albumin-binding domain for the selective immobilisation of recombinant capture antibody fragments on ELISA plates [J].
König, T ;
Skerra, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 218 (1-2) :73-83
[8]  
Kusnezow W, 2002, BIOTECHNIQUES, P14
[9]   High-throughput microarray-based enzyme-linked immunosorbent assay (ELISA) [J].
Mendoza, LG ;
McQuary, P ;
Mongan, A ;
Gangadharan, R ;
Brignac, S ;
Eggers, M .
BIOTECHNIQUES, 1999, 27 (04) :778-+
[10]   A perspective on protein microarrays [J].
Mitchell, P .
NATURE BIOTECHNOLOGY, 2002, 20 (03) :225-229