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

Authors
Lee, SeungahLee, ShinaeKo, Young-HoJung, HyungilKim, Jung DongSong, Joon MyongChoo, JaebumEo, Seong KugKang, Seong Ho
Issue Date
Apr-2009
Publisher
Elsevier
Keywords
Human leptin; Nanoarray protein chip; Single-molecule sandwich immunoassay; Total internal reflection fluorescence microscopy (TIRFM)
Citation
Talanta, v.78, no.2, pp 608 - 612
Pages
5
Journal Title
Talanta
Volume
78
Number
2
Start Page
608
End Page
612
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/46917
DOI
10.1016/j.talanta.2008.12.018
ISSN
0039-9140
1873-3573
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 = 456.35x + 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. © 2009 Elsevier B.V. All rights reserved.
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