Article

Quantitative analysis of human serum leptin using a nanoarray protein chip based on single-molecule sandwich immunoassay.

Department of Chemistry and Research Institute of Physics and Chemistry (RINPAC), Chonbuk National University, 664-14, 1-Ga, Duckjin-Dong, Duckjin-Gu, Jeonju 561-756, South Korea.
Talanta (impact factor: 3.79). 05/2009; 78(2):608-12. DOI:10.1016/j.talanta.2008.12.018 pp.608-12
Source: PubMed

ABSTRACT We report a method for the quantitative analysis of human serum leptin, which is a protein hormone associated with obesity, using a nanoarray protein chip based on a single-molecule sandwich immunoassay. The nanoarray patterning of a biotin-probe with a spot diameter of 150 nm on a self-assembled monolayer functionalized by MPTMS on a glass substrate was successfully accomplished using atomic force microscopy (AFM)-based dip-pen nanolithography (DPN). Unlabeled leptin protein molecules in human serum were detected based on the sandwich fluorescence immunoassay by total internal reflection fluorescence microscopy (TIRFM). The linear regression equation for leptin in the range of 100 zM-400 aM was determined to be y=456.35 x+80,382 (R=0.9901). The accuracy and sensitivity of the chip assay were clinically validated by comparing the leptin level in adult serum obtained by this method with those measured using the enzyme-linked immunosorbent assay (ELISA) performed with the same leptin standards and serum samples. In contrast to conventional ELISA techniques, the proposed chip methodology exhibited the advantages of ultra-sensitivity, a smaller sample volume and faster analysis time.

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Keywords

adult serum
 
AFM)-based dip-pen nanolithography
 
chip assay
 
conventional ELISA techniques
 
enzyme-linked immunosorbent assay
 
glass substrate
 
human serum
 
human serum leptin
 
leptin level
 
nanoarray patterning
 
nanoarray protein chip
 
proposed chip methodology exhibited
 
quantitative analysis
 
sandwich fluorescence immunoassay
 
serum samples
 
single-molecule sandwich immunoassay
 
smaller sample volume
 
spot diameter
 
ultra-sensitivity
 
Unlabeled leptin protein molecules