期刊
LANGMUIR
卷 35, 期 5, 页码 1266-1272出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.8b00810
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资金
- Australian Research Council [CE140100036]
- Australian Research Council [CE140100036] Funding Source: Australian Research Council
Development of antifouling films which selectively capture or target proteins of interest is essential for controlling interactions at the bio/nano interface. However, in order to synthesize biofunctional films from synthetic polymers that incorporate chemical motifs for surface immobilization, antifouling, and oriented biomolecule attachment, multiple reaction steps need to be carried out at the solid/liquid interface. EKx is a zwitterionic peptide that has previously been shown to have excellent antifouling properties. In this study, we recombinantly expressed EKx peptides and genetically encoded both surface attachment and antibody-binding motifs, before characterizing the resultant biopolymers by traditional methods. These peptides were then immobilized to organosilica nanoparticles for binding IgG, and subsequently capturing dengue NS1 as a model antigen from serum-containing solution. We found that a mixed layer of a short peptide (4.9 kDa) backfilled with a longer peptide terminated with an IgG-binding Z-domain (18 kDa) demonstrated selective capture of dengue NS1 protein down to similar to 10 ng mL(-1) in either PBS or 20% serum.
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