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Literature DB >> 21534617

Enantioselective recognition in biomimetic single artificial nanochannels.

Cuiping Han¹, Xu Hou, Huacheng Zhang, Wei Guo, Haibing Li, Lei Jiang.

Abstract

Efficient enantiomer discrimination with a convenient system remains a challenge in the fields of biochemistry, medical science, and pharmaceutics. Here we report a simple enantioselective sensing device based on a single artificial β-cyclodextrin-modified nanochannel system. This nanodevice shows highly selective recognition of histidine enantiomers through monitoring of ionic current signatures.

Entities: Chemical

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Year: 2011 PMID： 21534617 DOI： 10.1021/ja2004939

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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Cited

14 in total

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Enantioselective recognition in biomimetic single artificial nanochannels.

1. Stochastic sensing of proteins with receptor-modified solid-state nanopores.

2. Binomial distribution for quantification of protein subunits in biological nanoassemblies and functional nanomachines.

3. Simple and Versatile Detection of Viruses Using Anodized Alumina Membranes.

4. Incorporation of a viral DNA-packaging motor channel in lipid bilayers for real-time, single-molecule sensing of chemicals and double-stranded DNA.

5. Solid-State and Biological Nanopore for Real-Time Sensing of Single Chemical and Sequencing of DNA.

6. Selectively Sized Graphene-Based Nanopores for in Situ Single Molecule Sensing.

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Review 8. Nanopore-based analysis of biochemical species.

9. A light-regulated host-guest-based nanochannel system inspired by channelrhodopsins protein.

10. Fluoride responsive single nanochannel: click fabrication and highly selective sensing in aqueous solution.