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Ferritin and bovine serum albumin (BSA) proteins are chemically bonded to nitrogen-doped multi-walled carbon nanotubes (CNx MWNTs) through a two-step process of diimide-activated amidation. First, carboxylated CNx MWNTs were activated by N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDAC), forming a stable active ester in the presence of N-hydroxysuccinimide (NHS). Second, the active ester was reacted with the amine groups on the proteins of ferritin or BSA, forming an amide bond between the CNx MWNTs and proteins. This two-step process avoids the intermolecular conjugation of proteins, and guarantees the uniform attachment of proteins on carbon nanotubes. TEM and AFM measurements clearly confirmed the successful attachment. This approach provides a universal and efficient method to attach biomolecules to carbon nanotubes at ambient conditions.
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Kuiyang Jiang
Novarials (United States)
Linda S. Schadler
University of Vermont
Richard W. Siegel
Novartis (Switzerland)
Journal of Materials Chemistry
Washington State University
Pacific Northwest National Laboratory
Rensselaer Polytechnic Institute
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Jiang et al. (Tue,) studied this question.
synapsesocial.com/papers/6a1593675347fbb1739ffce2 — DOI: https://doi.org/10.1039/b310359e
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