Programmable high voltage CMOS chips for particle-based high-density combinatorial peptide synthesis

Abstract We built high voltage complementary metal oxide semiconductor (CMOS) chips that generate electrical fields on their surface, such that electrically charged microparticles (diameter 10–20 μm on average) can be addressed on distinct pixel electrodes according to arbitrary field patterns. Each pixel contains a memory cell in canonical low-voltage CMOS-technology controlling a high voltage (30–100 V) potential area on the top metal layer. Particle transfer with minimal contaminations in less than 10 s for a complete chip was observed for pixels of 100 μm × 100 μm down to 65 μm × 65 μm. This allows a new way to create surface modifications on top of CMOS chips without need for additional masks or stamps. Using suitable particles, a chemically modified chip surface, and compatible chemistry, this method can be utilized for self-aligned high-density biopolymer arrays, e.g., peptide arrays. Transfer of microparticles loaded with amino acids for combinatorial peptide synthesis is demonstrated. Successful synthesis of different peptides (octamers) was proven by immunostaining. Based on results obtained by a chip containing pixel areas of different characteristics, a chip for biological applications with 16,384 pixels (10,000 pixel/cm 2 ) was built. Good homogeneity of peptide synthesis over the chip area was verified by immunostaining.

[1]  Hussein Ballan,et al.  High Voltage Devices and Circuits in Standard CMOS Technologies , 1998 .

[2]  F. Bischoff,et al.  Precise selective deposition of microparticles on electrodes of microelectronic chips. , 2008, The Review of scientific instruments.

[3]  Volker Stadler,et al.  High-density peptide arrays. , 2009, Molecular bioSystems.

[4]  Volker Stadler,et al.  Multifunctional CMOS microchip coatings for protein and peptide arrays. , 2007, Journal of proteome research.

[5]  Volker Stadler,et al.  Combinatorial Synthesis of Peptide Arrays onto a Microchip , 2007, Science.

[6]  H. Baltes Enabling technology for MEMS and nanodevices , 2004 .

[7]  Heiko O. Jacobs,et al.  Approaching nanoxerography: The use of electrostatic forces to position nanoparticles with 100 nm scale resolution , 2002 .

[8]  Christian Paulus,et al.  CMOS-based DNA Sensor Arrays , 2004 .

[9]  C. Kim,et al.  Electrostatic funneling for precise nanoparticle placement: a route to wafer-scale integration. , 2007, Nano letters.

[10]  F. Bischoff,et al.  Particle‐Based Synthesis of Peptide Arrays , 2009, Chembiochem : a European journal of chemical biology.

[11]  H. Baltes,et al.  CMOS MEMS , 1997, Proceedings of 1997 IEEE International Symposium on Circuits and Systems. Circuits and Systems in the Information Age ISCAS '97.

[12]  A. Poustka,et al.  Combinatorial synthesis of peptide arrays with a laser printer. , 2008, Angewandte Chemie.

[13]  F. Breitling,et al.  A novel glass slide-based peptide array support with high functionality resisting non-specific protein adsorption. , 2006, Biomaterials.

[14]  T. Ludwig,et al.  PEGMA/MMA copolymer graftings: generation, protein resistance, and a hydrophobic domain. , 2008, Langmuir : the ACS journal of surfaces and colloids.