Methods for fabricating microarrays of motile bacteria

被引:61
作者
Rozhok, S
Shen, CKF
Littler, PLH
Fan, ZF
Liu, C
Mirkin, CA
Holz, RC
机构
[1] Univ Illinois, Microelect Lab 313, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Northwestern Univ, Inst Nanotechnol, Evanston, IL 60208 USA
[4] Utah State Univ, Dept Chem & Biochem, Logan, UT 84322 USA
关键词
arrays; atomic force microscopy; bacterial adhesion; dip-pen nanolithography; microcontact printing;
D O I
10.1002/smll.200400072
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Motile bacterial cell microarrays were fabricated by attaching Escherichia coli K-12 cells onto predesigned 16-mercaptohexadecanoic acid patterned microarrays, which were covalently functionalized with E. coli antibodies Or poly-L-lysine. By utilizing 11-mercaptoundecyl-penta-(ethylene glycol) or 11-mercapto-1-undecanol as passivating molecules, nonspecific binding of E. coli was significantly reduced. Microcontact printing and dip-pen nanolithography were used to prepare microarrays for bacterial adhesion, which was studied by optical fluorescence and atomic force microscopy. These data indicate that single motile E. coli can be attached to predesigned line or dot features and binding can occur via the cell body or the flagella of bacteria. Adherent bacteria are viable (remain alive and motile after adhesion to patterned surface features) for more than four hours. Individual motile bacterial cells can be placed onto predesigned surface features that are at least 1.3 mu m in diameter or larger. The importance of controlling the adhesion of single bacterial cell to a surface is discussed with regard to biomotor design.
引用
收藏
页码:445 / 451
页数:7
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