Submonolayer measurements of adsorbed proteins in microfluidic channels

被引:0
作者
Henry, David [2 ]
Lenghaus, Keith [1 ,2 ]
Wilson, Kerry A. [1 ,2 ]
Hirsch-Kuchma, Melissa [1 ]
Jenkins, Jerry [3 ]
Sundaram, Shankar [3 ]
Hickman, James J. [1 ,2 ]
机构
[1] Univ Cent Florida, 12424 Res Pkwy,Suite 400, Orlando, FL 32826 USA
[2] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
[3] CFD Res Corp, Huntsville, AL 35805 USA
来源
BIONANOTECHNOLOGY: PROTEINS TO NANODEVICES | 2006年
关键词
microfluidics; protein adsorption; CFD; XPS; simulation; flow;
D O I
10.1007/978-1-4020-4375-8_13
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microelectromechanical systems (MEMS), and soon nanoelectromechanical systems (NEMS), are projected to have a major impact in systems for toxin detection, proteomics and biomedical applications. This chapter describes experimental systems that were developed in our labs, as well as those being developed elsewhere, that are being used to understand protein deposition at sub-monolayer coverages in these devices. Modeling tools, used in conjunction with experimental results, can also be utilized for predicting the interactions of proteins with these microsystems, under static and flow conditions, with the goal of creating biocompatible MEMS devices that can be easily integrated with biologically based assay systems. The long-term combination and integration of biological and electronic components requires a thorough understanding of surface/biomolecule interactions in these devices. The use of surface modification techniques has allowed the tailoring of the interface between biological/nonbiological materials, independent of the bulk composition of the nonbiological material, to enable reproducible experimental design. Our results to date have indicated we can measure protein adsorption down to less that 1% of a monolayer and that static results are very different than those observed under flow conditions, and this has been supported by the modeling results. Thus, data obtained under static conditions cannot be used as a predictor for behavior under flow conditions, which should be the predominant situation in most biological assay systems.
引用
收藏
页码:257 / 274
页数:18
相关论文
共 52 条
[1]  
BRIGGS MP, 1992, PRACTICAL SURFACE AN
[2]   Protein adsorption onto polystyrene surfaces studied by XPS and AFM [J].
Browne, MM ;
Lubarsky, GV ;
Davidson, MR ;
Bradley, RH .
SURFACE SCIENCE, 2004, 553 (1-3) :155-167
[3]  
Butler J. E., 1993, Molecular Immunology, V30, P1165, DOI 10.1016/0161-5890(93)90135-X
[4]   Adsorption-induced antigenic changes and their significance in ELISA and immunological disorders [J].
Butler, JE ;
Navarro, P ;
Sun, J .
IMMUNOLOGICAL INVESTIGATIONS, 1997, 26 (1-2) :39-54
[5]  
BUTLER JE, 1981, METHOD ENZYMOL, P482
[6]   Raman dye-labeled nanoparticle probes for proteins [J].
Cao, YC ;
Jin, RC ;
Nam, JM ;
Thaxton, CS ;
Mirkin, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14676-14677
[7]  
CHAKRABORTY A, 2004, P SIMBIOSYS PI M PAL
[8]   Molecular monolayers and interfacial electron transfer of Pseudomonas aeruginosa azurin on Au(111) [J].
Chi, QJ ;
Zhang, JD ;
Nielsen, JU ;
Friis, EP ;
Chorkendorff, I ;
Canters, GW ;
Andersen, JET ;
Ulstrup, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (17) :4047-4055
[9]   Adsorption and bioactivity of protein A on silicon surfaces studied by AFM and XPS [J].
Coen, MC ;
Lehmann, R ;
Gröning, P ;
Bielmann, M ;
Galli, C ;
Schlapbach, L .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 233 (02) :180-189
[10]   Metal-polymer nanocomposites for integrated microfluidic separations and surface enhanced Raman spectroscopic detection [J].
Connatser, RM ;
Riddle, LA ;
Sepaniak, MJ .
JOURNAL OF SEPARATION SCIENCE, 2004, 27 (17-18) :1545-1550