TY - JOUR
T1 - Programmable microbial ink for 3D printing of living materials produced from genetically engineered protein nanofibers
AU - Duraj-Thatte, Anna M.
AU - Manjula-Basavanna, Avinash
AU - Rutledge, Jarod
AU - Xia, Jing
AU - Hassan, Shabir
AU - Sourlis, Arjirios
AU - Rubio, Andrés G.
AU - Lesha, Ami
AU - Zenkl, Michael
AU - Kan, Anton
AU - Weitz, David A.
AU - Zhang, Yu Shrike
AU - Joshi, Neel S.
N1 - Funding Information:
Work was performed in part at the Center for Nanoscale Systems at Harvard. Work in the N.S.J. laboratory is supported by the National Institutes of Health (1R01DK110770), the National Science Foundation (DMR 2004875), and the Wyss Institute for Biologically Inspired Engineering at Harvard University. Work in the D.A.W. laboratory is supported by the Harvard University Materials Research Science and Engineering Center (NSF Grants DMR-1420570 and DMR-2011754). Work in the Y.S.Z. laboratory was supported by the Lush Prize and the Brigham Research Institute. Parts of the schematics were adapted from BioRender.com.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Living cells have the capability to synthesize molecular components and precisely assemble them from the nanoscale to build macroscopic living functional architectures under ambient conditions. The emerging field of living materials has leveraged microbial engineering to produce materials for various applications but building 3D structures in arbitrary patterns and shapes has been a major challenge. Here we set out to develop a bioink, termed as “microbial ink” that is produced entirely from genetically engineered microbial cells, programmed to perform a bottom-up, hierarchical self-assembly of protein monomers into nanofibers, and further into nanofiber networks that comprise extrudable hydrogels. We further demonstrate the 3D printing of functional living materials by embedding programmed Escherichia coli (E. coli) cells and nanofibers into microbial ink, which can sequester toxic moieties, release biologics, and regulate its own cell growth through the chemical induction of rationally designed genetic circuits. In this work, we present the advanced capabilities of nanobiotechnology and living materials technology to 3D-print functional living architectures.
AB - Living cells have the capability to synthesize molecular components and precisely assemble them from the nanoscale to build macroscopic living functional architectures under ambient conditions. The emerging field of living materials has leveraged microbial engineering to produce materials for various applications but building 3D structures in arbitrary patterns and shapes has been a major challenge. Here we set out to develop a bioink, termed as “microbial ink” that is produced entirely from genetically engineered microbial cells, programmed to perform a bottom-up, hierarchical self-assembly of protein monomers into nanofibers, and further into nanofiber networks that comprise extrudable hydrogels. We further demonstrate the 3D printing of functional living materials by embedding programmed Escherichia coli (E. coli) cells and nanofibers into microbial ink, which can sequester toxic moieties, release biologics, and regulate its own cell growth through the chemical induction of rationally designed genetic circuits. In this work, we present the advanced capabilities of nanobiotechnology and living materials technology to 3D-print functional living architectures.
UR - http://www.scopus.com/inward/record.url?scp=85119821751&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-26791-x
DO - 10.1038/s41467-021-26791-x
M3 - Article
C2 - 34815411
AN - SCOPUS:85119821751
SN - 2041-1723
VL - 12
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6600
ER -