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Title 

Single-protein molecular interactions on polymer-modified glass substrates for nanoarray chip application using dual-color TIRFM

Authors 

D KimHee Gu LeeH JungS H Kang

Publisher 

The Korean Chemical Society

Issue Date 

2007

Citation 

Bulletin of the Korean Chemical Society, vol. 28, no. 5, pp. 783-790

Keywords 

dual-color TIRFMnanoarray protein chippolymer-modified glasssingle-molecule detectionbiochipspolymeric glassnanoarray protein chipssingle molecule detectionproteins

Abstract 

The immobilization of proteins and their molecular interactions on various polymer-modified glass substrates [i.e. 3-aminopropyltriethoxysilane (APTS), 3-glycidoxypropyltrimethoxysilane (GPTS), poly (ethylene glycol) diacrylate (PEG-DA), chitosan (CHI), glutaraldehyde (GA), 3-(trichlorosilyl)propyl methacrylate (TPM), 3'-mercaptopropyltrimethoxysilane (MPTMS), glycidyl methacrylate (GMA) and poly-l-lysine (PL).] for potential applications in a nanoarray protein chip at the single-molecule level was evaluated using prism-type dual-color total internal reflection fluorescence microscopy (dual-color TIRFM). A dual-color TIRF microscope, which contained two individual laser beams and a single high-sensitivity camera, was used for the rapid and simultaneous dual-color detection of the interactions and colocalization of different proteins labeled with different fluorescent dyes such as Alexa Fluor® 488, Qdot® 525 and Alexa Fluor® 633. Most of the polymer-modified glass substrates showed good stability and a relative high signal-to-noise (S/N) ratio over a 40-day period after making the substrates. The GPTS/CHI/GA-modified glass substrate showed a 13.5-56.3% higher relative S/N ratio than the other substrates. 1% Top-Block in 10 mM phosphate buffered saline (pH 7.4) showed a 99.2% increase in the blocking effect of non-specific adsorption. These results show that dual-color TIRFM is a powerful methodology for detecting proteins at the single-molecule level with potential applications in nanoarray chips or nano-biosensors.

ISSN 

0253-2964

Link 

http://dx.doi.org/10.5012/bkcs.2007.28.5.783

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2019-05-02


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