Abstract

Carbon nanotubes (CNTs) have already been considered for medical applications due to their small diameter and ability to penetrate cells and tissues. However, since CNTs are chemically inert and non-dispersible in water, they have to be chemically functionalized or coated with biomolecules to carry payloads or interact with the environment. Proteins, although often only randomly bound to the CNT surface, are preferred because they provide a better biocompatibility and present functional groups for binding additional molecules. A new approach to functionalize CNTs with a closed and precisely ordered protein layer is offered by bacterial surface layer (S-layer) proteins, which have already attracted much attention in the functionalization of surfaces. We could demonstrate that bacterial S-layer proteins (SbpA of Lysinibacillus sphaericus CCM 2177 and the recombinant fusion protein rSbpA31-1068GG comprising the S-layer protein and two copies of the IgG binding region of Protein G) can be used to disperse and functionalize oxidized multi walled CNTs. Following a simple protocol, a complete surface coverage with a long-range crystalline S-layer lattice can be obtained. When rSbpA31-1068GG was used for coating, the introduced functionality could be confirmed by binding gold labeled antibodies via the IgG binding domain of the fusion protein. Since a great variety of functional S-layer fusion proteins has already been described, our new technology has the potential for a broad spectrum of functionalized CNTs.

Highlights

  • Since their discovery, carbon nanotubes (CNTs) have already been intensively investigated and characterized in material sciences due to their outstanding mechanical, electrical, and thermal properties [1,2,3,4]

  • We could demonstrate that bacterial surface layer (S-layer) proteins (SbpA of Lysinibacillus sphaericus CCM 2177 and the recombinant fusion protein rSbpA31-1068 GG comprising the S-layer protein and two copies of the IgG binding region of Protein G) can be used to disperse and functionalize oxidized multi walled Carbon nanotubes (CNTs)

  • silicon have shown that the S-layer did not resemble the silicon crystal structure experiments gold surfaces nanoparticles were not found on wild type SbpA (wtSbpA)

Read more

Summary

Introduction

Carbon nanotubes (CNTs) have already been intensively investigated and characterized in material sciences due to their outstanding mechanical, electrical, and thermal properties [1,2,3,4]. The formation of monolayers on technologically important substrates, as or glass,orwas always major concern the development of affinity matrices, biosensing or the silicon glass, wasaalways a majorfor concern for the development of affinity matrices,layers biosensing development of organic-inorganic hybrid architectures. In this context, as a further layers or the development of organic-inorganic hybrid[24,27]. (p4) lattice lattice symmetry on CNTs. 13.1 nm, we decided to symmetry on CNTs. With respect to the unit cell size of SbpA with 13.1 × 13.1 nm, we decided work with multiwalled nanotubes (MWNTs) with diameters ranging from.

Schematic
Production of Wild Type and Recombinant S-Layer Fusion Protein Solutions
Lwas water
Coating of -COOH Functionalized MWNTs with S-Layer Proteins
Immuno Gold Labeling of rSbpA31-1068 GG Coated -COOH Functionalized MWNTs
Preparation of Bucky Paper and Scanning Electron Microscopy
Results
Coating of -COOH Functionalized MWNTs with wtSbpA S-Layer Protein
Coating of -COOH Functionalized MWNTs with rSbpA31-1068 GG Fusion Protein
Dispersiongold of -COOH
Dispersion of -COOH Functionalized MWNTs by Addition of Triton-X 100
Discussion
Summary
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call