Dynamic inking of large-scale stamps for multiplexed microcontact printing and fabrication of cell microarrays

PLoS One. 2018 Aug 23;13(8):e0202531. doi: 10.1371/journal.pone.0202531. eCollection 2018.

Abstract

Microcontact printing has become a versatile soft lithography technique used to produce molecular micro- and nano-patterns consisting of a large range of different biomolecules. Despite intensive research over the last decade and numerous applications in the fields of biosensors, microarrays and biomedical applications, the large-scale implementation of microcontact printing is still an issue. It is hindered by the stamp-inking step that is critical to ensure a reproducible and uniform transfer of inked molecules over large areas. This is particularly important when addressing application such as cell microarray manufacturing, which are currently used for a wide range of analytical and pharmaceutical applications. In this paper, we present a large-scale and multiplexed microcontact printing process of extracellular matrix proteins for the fabrication of cell microarrays. We have developed a microfluidic inking approach combined with a magnetic clamping technology that can be adapted to most standard substrates used in biology. We have demonstrated a significant improvement of homogeneity of printed protein patterns on surfaces larger than 1 cm2 through the control of both the flow rate and the wetting mechanism of the stamp surface during microfluidic inking. Thanks to the reproducibility and integration capabilities provided by microfluidics, we have achieved the printing of three different adhesion proteins in one-step transfer. Selective cell adhesion and cell shape adaptation on the produced patterns were observed, showing the suitability of this approach for producing on-demand large-scale cell microarrays.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques
  • Cell Adhesion / genetics
  • Cell Shape / genetics
  • Extracellular Matrix Proteins / chemistry
  • Extracellular Matrix Proteins / isolation & purification*
  • Microfluidic Analytical Techniques / methods*
  • Printing / instrumentation*
  • Tissue Array Analysis / instrumentation*

Substances

  • Extracellular Matrix Proteins

Grants and funding

Agence nationale pour la recherche (ANR) www.agence-nationale-recherche.fr LABCOM program: ANR-13-LAB2-0009-01