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1.
J Am Chem Soc ; 138(3): 746-9, 2016 Jan 27.
Article in English | MEDLINE | ID: mdl-26694542

ABSTRACT

The direct incorporation of macrocyclic cyclidene complexes into DNA via automated synthesis results in a new family of metal-functionalized DNA derivatives that readily demonstrate their utility through the ability of one redox-active copper(II)-containing strand to distinguish electrochemically between all four canonical DNA nucleobases at a single site within a target sequence of DNA.


Subject(s)
DNA/chemistry , Electrochemical Techniques , Macrocyclic Compounds/chemistry , Nucleotides/analysis , Organometallic Compounds/chemistry , Molecular Structure
2.
ACS Synth Biol ; 4(12): 1316-25, 2015 Dec 18.
Article in English | MEDLINE | ID: mdl-26046486

ABSTRACT

The field of synthetic biology includes studies that aim to develop new materials and devices from biomolecules. In recent years, much work has been carried out using a range of biomolecular chassis including α-helical coiled coils, ß-sheet amyloids and even viral particles. In this work, we show how hybrid bionanoparticles can be produced from a viral M13 bacteriophage scaffold through conjugation with DNA primers that can template a polymerase chain reaction (PCR). This unprecedented example of a PCR on a virus particle has been studied by flow aligned linear dichroism spectroscopy, which gives information on the structure of the product as well as a new protototype methodology for DNA detection. We propose that this demonstration of PCR on the surface of a bionanoparticle is a useful addition to ways in which hybrid assemblies may be constructed using synthetic biology.


Subject(s)
Bacteriophage M13/chemistry , DNA Primers/chemistry , Nanoparticles/chemistry , Polymerase Chain Reaction/methods
3.
Dalton Trans ; 44(16): 7268-75, 2015 Apr 28.
Article in English | MEDLINE | ID: mdl-25791522

ABSTRACT

A new series of chiral ureas containing one or two redox-active ferrocene units was synthesised and studied in order to investigate the effect of planar chirality and central chirality on electrochemical chiral sensing. Binding of chiral carboxylate anions in organic solvents through H-bond formation caused a negative shift in the potentials of the ferrocene/ferrocenium (Fc/Fc(+)) couples of the receptors, demonstrating their use as electrochemical sensors in solution. While the presence of two ferrocene units gave no marked improvement in the chiral sensing capabilities of these systems, the introduction of planar chirality, in addition to central chirality, switched the enantiomeric binding preference of the system and also caused an interesting change in the appearance of some voltammograms, with unusual two-wave behaviour observed upon binding a protected prolinate guest.

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