A force-based protein biochip

被引:51
|
作者
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
机构
[1] Lehrstuhl Angew Phys, D-08799 Munich, Germany
[2] Ctr NanoSci, D-08799 Munich, Germany
[3] Nanotype, D-82166 Grafelfing, Germany
[4] Drug Discovery Johnson & Johnson Pharmaceut Res &, Raritan, NJ 08869 USA
[5] Orthoclin Diagnost, Raritan, NJ 08869 USA
关键词
D O I
10.1073/pnas.1934928100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A parallel assay for the quantification of single-molecule binding forces was developed based on differential unbinding force measurements where ligand-receptor interactions are compared with the unzipping forces of DNA hybrids. Using the DNA zippers as molecular force sensors, the efficient discrimination between specific and nonspecific interactions was demonstrated for small molecules binding to specific receptors, as well as for protein-protein interactions on protein arrays. Finally, an antibody sandwich assay with different capture antibodies on one chip surface and with the detection antibodies linked to a congruent surface via the DNA zippers was used to capture and quantify a recombinant hepatitis C antigen from solution. In this case, the DNA zippers enable not only discrimination between specific and nonspecific binding, but also allow for the local application of detection antibodies, thereby eliminating false-positive results caused by cross-reactive antibodies and nonspecific binding.
引用
收藏
页码:11356 / 11360
页数:5
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