The use of nanoarrays for highly sensitive and selective detection of human immunodeficiency virus type 1 in plasma

被引:192
作者
Lee, KB
Kim, EY
Mirkin, CA
Wolinsky, SM
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL USA
[2] Northwestern Univ, Inst Nanotechnol, Evanston, IL USA
[3] Northwestern Univ, Feinberg Sch Med, Div Infect Dis, Chicago, IL 60611 USA
关键词
D O I
10.1021/nl049002y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Arrays of antibodies with well-defined feature size and spacing are necessary for developing highly sensitive and selective immunoassays to detect macromolecules in complex solutions. Here we report the application of nanometer-scale antibody array-based analysis to determine the presence of the human immunodeficiency virus type 1 (HIV-1) in blood samples. Dip-pen nanolithography (DPN) was used to generate nanoscale patterns of antibodies against the HIV-1 p24 antigen on a gold surface. Feature sizes were less than 100-nanometers, and the activity of the antibody was preserved. HIV-1 p24 antigen in plasma obtained directly from HIV-1-infected patients was hybridized to the antibody array in situ, and the bound protein was hybridized to a gold antibody-functionalized nanoparticle probe for signal enhancement. The nanoarray features in the three-component sandwich assay were confirmed by atomic force microscopy (AFM). Demonstration of measurable amounts of HIV-1 p24 antigen in plasma obtained from men with less than 50 copies of RNA per ml of plasma (corresponding to 0.025 pg per ml) illustrates that the nanoarray-based assay can exceed the limit of detection of conventional enzyme-linked immunosorbent assay (ELISA)based immunoassays (5 pg per ml of plasma) by more than 1000-fold.
引用
收藏
页码:1869 / 1872
页数:4
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