We have generated mesoscopic patterns of viable Escherichia coli on Si(1 1
1), glass, and nutrient agar plates by using a novel laser-based transfer p
rocess termed matrix assisted pulsed laser evaporation direct write (MAPLE
DW). We observe no alterations to the E. coli induced by the laser-material
interaction or the shear forces during the transfer. Transferred E. coli p
atterns were observed by optical and electron microscopes, and cell viabili
ty was shown through green fluorescent protein (GFP) expression and cell cu
lturing experiments. The transfer mechanism for our approach appears remark
ably gentle and suggests that active biomaterials such as proteins, DNA and
antibodies could be serially deposited adjacent to viable cells. Furthermo
re, this technique is a direct write technology and therefore does not invo
lve the use of masks, etching, or other lithographic tools. (C) 2001 Elsevi
er Science Ltd. All rights reserved.