Probing Selective Self-Assembly of Putrescine Oxidase with Controlled Orientation Using a Genetically Engineered Peptide Tag

Langmuir ◽  
2021 ◽  
Author(s):  
Nilan J. B. Kamathewatta ◽  
Tyler M. Nguyen ◽  
Rachel Lietz ◽  
Talisa Hughes ◽  
Banu Taktak Karaca ◽  
...  
2004 ◽  
Vol 126 (41) ◽  
pp. 13212-13213 ◽  
Author(s):  
Javier Reguera ◽  
Amir Fahmi ◽  
Philip Moriarty ◽  
Alessandra Girotti ◽  
José Carlos Rodríguez-Cabello

2021 ◽  
Author(s):  
Anna M Duraj-Thatte ◽  
Avinash Manjula Basavanna ◽  
Jarod Rutledge ◽  
Jing Xia ◽  
Shabir Hassan ◽  
...  

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. We set out to develop a new 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. This report showcases the advanced capabilities of nanobiotechnology and living materials technology to 3D-print functional living architectures.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Anna M. Duraj-Thatte ◽  
Avinash Manjula-Basavanna ◽  
Jarod Rutledge ◽  
Jing Xia ◽  
Shabir Hassan ◽  
...  

AbstractLiving 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.


2011 ◽  
Vol 12 (11) ◽  
pp. 3844-3850 ◽  
Author(s):  
Xiao-Xia Xia ◽  
Qiaobing Xu ◽  
Xiao Hu ◽  
Guokui Qin ◽  
David L. Kaplan

2001 ◽  
Vol 7 (S2) ◽  
pp. 992-993
Author(s):  
Hanson Fong ◽  
Daniel Heidel ◽  
Mehmet Sarikaya ◽  
Michael Paine ◽  
Wen Lou ◽  
...  

Dental enamel is the most durable bioceramics produced by a vertebrate as it is designed to perform masticatory functions throughout its lifetime. The understanding of the mechanism of enamel formation and effects of proteins during the biomineralization process are fundamental issues, essential for both potential enamel regeneration and as a base for synthesis, via self-assembly, of biomimetic composites.The biomineralization process of enamel is carried out by ameloblast cells that line the inner enamel epithelium and secrete an extracellular protein matrix onto a mineralized dentin surface at the dentin-enamel junction (DEJ). A major matrix protein, amelogenin, is believed to regulate the mineralization of hydroxyapatite (HAP) in the enamel tissue. It has been shown to undergo self-assembly in vitro and in vivo to form nanospheres of ∼20nm in diameter. Previous TEM studies have shown that the nanospheres align along the length (c-axis) of hydroxyapatite (HA) crystals. There are two domains, namely A (residues 1-42) and B (residues 157-173), that control the self-assembly behavior of the nanospheres.


Author(s):  
Candan Tamerler ◽  
Mehmet Sarikaya

Nature provides inspiration for designing materials and systems that derive their functions from highly organized structures. Biological hard tissues are hybrid materials having inorganics within a complex organic matrix, the molecular scaffold controlling the inorganic structures. Biocomposites incorporate both biomacromolecules such as proteins, lipids and polysaccharides, and inorganic materials, such as hydroxyapatite, silica, magnetite and calcite. The ordered organization of hierarchical structures in organisms begins via the molecular recognition of inorganics by proteins that control interactions and is followed by the highly efficient self-assembly across scales. Following the molecular biological principle, proteins could also be used in controlling materials formation in practical engineering via self-assembled, hybrid, functional materials structures. In molecular biomimetics, material-specific peptides could be the key in the molecular engineering of biology-inspired materials. With the recent developments of nanoscale engineering in physical sciences and the advances in molecular biology, we now combine genetic tools with synthetic nanoscale constructs to create a novel methodology. We first genetically select and/or design peptides with specific binding to functional solids, tailor their binding and assembly characteristics, develop bifunctional peptide/protein genetic constructs with both material binding and biological activity, and use these as molecular synthesizers, erectors and assemblers. Here, we give an overview of solid-binding peptides as novel molecular agents coupling bio- and nanotechnology.


2005 ◽  
Vol 2 (4) ◽  
pp. 317-326 ◽  
Author(s):  
Kenneth H. Sandhage ◽  
Shawn M. Allan ◽  
Matthew B. Dickerson ◽  
Christopher S. Gaddis ◽  
Samuel Shian ◽  
...  

ACS Nano ◽  
2009 ◽  
Vol 3 (6) ◽  
pp. 1525-1531 ◽  
Author(s):  
Christopher R. So ◽  
John L. Kulp ◽  
Ersin Emre Oren ◽  
Hadi Zareie ◽  
Candan Tamerler ◽  
...  

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