Cell-Directed Assembly of Lipid-Silica Nanostructures Providing Extended Cell Viability

Author:

Baca Helen K.12345,Ashley Carlee12345,Carnes Eric12345,Lopez Deanna12345,Flemming Jeb12345,Dunphy Darren12345,Singh Seema12345,Chen Zhu12345,Liu Nanguo12345,Fan Hongyou12345,López Gabriel P.12345,Brozik Susan M.12345,Werner-Washburne Margaret12345,Brinker C. Jeffrey12345

Affiliation:

1. Department of Chemical and Nuclear Engineering, University of New Mexico, Albuquerque, NM 87185, USA.

2. Sandia National Laboratories, Albuquerque, NM 87185, USA.

3. Los Alamos National Laboratory, Chemistry Division, Los Alamos, NM 87545, USA.

4. Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.

5. Department of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque, NM 87131, USA.

Abstract

Amphiphilic phospholipids were used to direct the formation of biocompatible, uniform silica nanostructures in the presence of Saccharomyces cerevisiae and bacterial cell lines. The cell surfaces organize multilayered phospholipid vesicles that interface coherently with the silica host and help relieve drying stresses that develop with conventional templates. These host structures maintain cell accessibility, addressability, and viability in the absence of buffer or an external fluidic architecture. The cell surfaces are accessible and can be used to localize added proteins, plasmids, and nanocrystals. Prolonged cell viability combined with reporter protein expression enabled stand-alone cell-based sensing.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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