Si nanocolumns as novel nanostructured supports for enzyme immobilization

被引:20
作者
Yim, TJ
Kim, DY
Karajanagi, SS
Lu, TM
Kane, R [1 ]
Dordick, JS
机构
[1] Rensselaer Polytech Inst, Dept Biol & Chem Engn, Troy, NY 12180 USA
[2] Rensselaer Polytech Inst, Dept Phys, Troy, NY 12180 USA
[3] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
关键词
glancing angle deposition; nanocolumns; soybean peroxidase; biocatalysis; enzyme immobilization; nanotechnology;
D O I
10.1166/jnn.2003.240
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silicon nanocolumns have been used as novel supports for the high-density immobilization of enzymes. Silicon nanocolumns with diameters of ca. 50-100 nm and a height of 1 mum were constructed using glancing angle deposition. The surfaces were successively treated with 3-amino-propyltriethoxysilane (APTES) and then with an amine reactive polymer, poly(ethylene-alt-maleic anhydride), to attach soybean peroxidase (SBP) to the support. Optimal coverage of APTES, polymer, and SBP was obtained for incorporation of enzyme onto the sidewalls of the nanocolumns. SBP immobilized on the silicon nanocolumns demonstrated an enhancement in biocatalytic activity of 160% over that of the enzyme immobilized on flat silicon wafers with the same projected area. The enzymatic activity decreased with progressive washes for both supports. This decrease in the activity of enzyme was found to be primarily due to the intrinsic deactivation of immobilized enzyme on the silicon surface. Designing nanocolumns with optimal dimensions, spacing, and surface chemistry may lead to the development of high-density arrays of proteins for applications in biotechnology.
引用
收藏
页码:479 / 482
页数:4
相关论文
共 23 条
[1]   PEROXIDASE-CATALYZED POLYMERIZATION AND DEPOLYMERIZATION OF COAL IN ORGANIC-SOLVENTS [J].
BLINKOVSKY, AM ;
MCELDOON, JP ;
ARNOLD, JM ;
DORDICK, JS .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1994, 49 (02) :153-164
[2]  
CONNOLLY S, 1999, ADV MATER, V1202, P449
[3]  
Engasser J.-M., 1976, APPLIED BIOCHEMISTRY, V1, P127
[4]   A WATER-INSOLUBLE POLYANIONIC DERIVATIVE OF TRYPSIN .2. EFFECT OF POLYELECTROLYTE CARRIER ON KINETIC BEHAVIOR OF BOUND TRYPSIN [J].
GOLDSTEIN, L ;
LEVIN, Y ;
KATCHALSKI, E .
BIOCHEMISTRY, 1964, 3 (12) :1913-+
[5]   Activity, stability and conformational flexibility of seed coat soybean peroxidase [J].
Kamal, JKA ;
Behere, DV .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2003, 94 (03) :236-242
[6]   Multienzyme catalysis in microfluidic biochips [J].
Lee, MY ;
Srinivasan, A ;
Ku, B ;
Dordick, JS .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 83 (01) :20-28
[7]   Protein-resistant coatings for glass and metal oxide surfaces derived from oligo(ethylene glycol)-terminated alkyltrichlorosilanes [J].
Lee, SW ;
Laibinis, PE .
BIOMATERIALS, 1998, 19 (18) :1669-1675
[8]   A WATER-INSOLUBLE POLYANIONIC DERIVATIVE OF TRYPSIN .I. PREPARATION AND PROPERTIES [J].
LEVIN, Y ;
PECHT, M ;
GOLDSTEIN, L ;
KATCHALSKI, E .
BIOCHEMISTRY, 1964, 3 (12) :1905-+
[9]  
Ma PX, 1999, J BIOMED MATER RES, V46, P60, DOI 10.1002/(SICI)1097-4636(199907)46:1<60::AID-JBM7>3.0.CO
[10]  
2-H