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Biomedical subjects

James N Wilson

Publications and source records attributed to James N Wilson.

15 recordsLinked to original sources

Fluorescent DNA base replacements: Reporters and sensors for biological systems.

We describe the design, synthesis, and properties of nucleoside monomers in which the DNA base is replaced by fluorescent hydrocarbons and heterocycles, and the assembly of these monomers into DNA-like molecules in which the all bases are fluorescent. As monomers, such molecules have useful applications as reporters in the DNA context. The use of fluorescent DNA bases, rather than more traditional fluorophores tethered to the DNA strand, gives a more predictable location and orientation, and yields a more direct response to changes that occur within the helix. In addition to uses as monomers, such compounds can be assembled into polychromophoric oligomers ("oligodeoxyfluorosides" or ODFs). ODFs are water soluble, discrete molecules and are easily arranged into specific sequences by use of a DNA synthesizer. They have displayed a number of properties not readily available in commercial fluorophores, including large Stokes shifts, tunable excitation and emission wavelengths, and sensing responses to physical changes or molecular species in solution. We describe an approach to assembling and screening large sets of oligofluorosides for rapid identification of molecules with desirable properties. Such compounds show promise for applications in biochemistry, biology, environmental and materials applications.

Adenosine Monophosphate↗

Cruciforms as functional fluorophores: response to protons and selected metal ions.

The photophysics of dialkylamino- and/or pyridine-containing functional chromophores, 1,4-distyryl-2,5-bis(ethynylaryl)benzenes (cruciforms) was investigated; their fluorescence quantum yields and emissive lifetimes were determined. Depending upon their substituents, the frontier molecular orbitals (FMOs) of these cruciforms are either congruent, i.e., HOMO and LUMO occupy the same real space, or disjoint, i.e., the HOMO is located on one branch of the cruciform while the LUMO is located on the second one. Donor-acceptor substitution leads to a disjoint FMO pattern, while the parent 1,4-distyryl-2,5-bis(phenylethynyl)benzene shows congruent FMOs. The photophysics of the cruciforms was investigated upon addition of either an excess of trifluoroacetic acid or an excess of selected metal (Mg(2+), Ca(2+), Mn(2+), Zn(2+)) trifluoromethanesulfonate salts. Addition of either metal ions or protons led to analogous but not identical changes in the spectroscopic properties of the investigated cruciforms. The collected data suggest that the metals bind preferentially at the aniline nitrogen and not at the electron-rich arene. The spatially separated FMOs permit the independent manipulation of the HOMO and the LUMO of such cruciforms. If the branches contain metal-complexing moieties, metal binding leads to either a hypsochromic or a bathochromic shift in emission via interaction of the metal cations with either the HOMO or the LUMO.

Journal Article↗

Reduced fluorescence quenching of cyclodextrin-acetylene dye rotaxanes.

An acetylene dye rotaxane with alpha-CD has been synthesized using the Heck-Cassar-Sonogashira-Hagihara-type reaction in aqueous solution. Free dye with tetracarboxylic acids is found to be highly sensitive to various metal ions, showing high Stern-Volmer constants, KSV. As CD encapsulation protects and stabilizes the threaded chromophore against an outside quencher, metal-insensitive biological tags are an obvious application for this class of molecules.

Journal Article↗

Supramolecular cruciforms.

By self-assembling fluorescent pyridyl cruciforms with bis-Pd-pincer complexes, supramolecular assemblies with attractive optical properties were synthesized; these assemblies show potential as electro-optical materials.

Journal Article↗

New designs for DNA bases: expanded DNAs and oligofluorosides.

Properties and applications of two new classes of DNA base replacements are described. The first class is size-expanded DNA bases; these are benzo-homologous versions of A, C, T, G that yield base pairs 2.4 Angstroms larger than natural pairs. New studies have explored the ability of expanded DNA base pairs to be replicated by DNA polymerase enzymes. The second class of DNA-like molecules described here are "oligodeoxyfluorosides" (ODFs), which are deoxyribose-phosphate oligomers in which all nucleobases are replaced by hydrocarbon and heterocyclic fluorophores. These compounds have been prepared in large libraries and have been screened for unusual fluorescence and sensing properties.

Adenine↗

Switching of intramolecular charge transfer in cruciforms: metal ion sensing.

Three different cruciforms containing the 1,4-bis-4'-pyridylethynyl-2,5-distyrylbenzene or the 1,4-bis-phenylethynyl-2,5-distyrylbenzene unit were synthesized and investigated with respect to their metal sensing properties. Upon addition of metal cations to these cruciforms, either a bathochromic or hypsochromic shift in emission and absorption is observed. The shift depends on whether the metal coordinates preferentially to the pyridine or to the dibutylaniline branches of the cruciforms. The three cruciforms were exposed to a selection of metal cations in dichloromethane, and their emission was examined. The cruciforms show differential sensing of metal cations, that is, different metals can be specifically discerned upon exposure to three cruciforms but not when exposed to only one. The system can discern calcium from magnesium cations and silver from mercury or lithium cations.

Journal Article↗

Sugar-poly(para-phenylene ethynylene) conjugates as sensory materials: efficient quenching by Hg2+ and Pb2+ ions.

Three polar poly(para-phenylene ethynylene)s (PPE) were synthesized by utilizing the Heck-Sonogashira protocol. Two of the PPEs carry beta-glucopyranose substituents. Depending upon the linker used between the glycol units and the backbone, the fluorescence of these PPEs can be quenched by Hg2+ and Pb2+ to a varying degree. Monomeric model compounds that are substituted with only one glucose unit are not efficiently quenched. The presence of many glucose substituents in one PPE assembly led to a large increase in the binding constant to Hg2+ and quenching of the fluorescence was amplified.

Alkynes↗

Cruciform pi-systems: effect of aggregation on emission.

The solid state properties of cruciform pentamers are examined in thin film preparation, in the single crystalline state and in nanoparticle formulations; emission behavior was found to vary substantially with the solid state morphology. This type of behaviour is an excellent way to manipulate the emissive properties of conjugated [small pi]-systems.

Journal Article↗

Permanent bubble arrays from a cross-linked poly(para-phenyleneethynylene): picoliter holes without microfabrication.

An azide-substituted poly(para-phenyleneethynylene) (PPE) 4 was prepared by the Heck-Cassar-Sonogashira-Hagihara method. Thin films of 4 form self-assembled bubble arrays from carbon disulfide solution utilizing the breath figure method. The as-formed porous films of 4 are soluble in common solvents, and the air bubbles are interconnected. Upon heating to 300 degrees C, 4 cross-links and the thin film turn into insoluble matrix with isolated bubbles. The cross-linking process has transformed the bubble arrays of 4 into insoluble picoliter beakers or picoliter vials, whose diameters are approximately 3.0 and 1.5 mum at the top and bottom, respectively.

Journal Article↗

Chiroptical properties of poly(p-phenyleneethynylene) copolymers in thin films: large g-values.

A series of chirally substituted poly (p-phenyleneethynylene) copolymers was prepared by alkyne metathesis of mixtures of two different 2,5-dialkyl-1,4-dipropynylbenzenes. One of the monomers was the chiral bis-2,5-(S)-3,7-dimethyloctyl-1,4-dipropynylbenzene, and the second one was an achiral dipropynyl monomer. If the content of chiral monomer is 25-50 mol %, unusually large chiroptical effects, that is, optical dissymmetries, result in absorption (g = -0.38) and emission (g = -0.19) of these copolymers. The large dissymmetries can be explained by a supramolecular ordering of the PPEs into stranded features that are visualized by dark-field transmission electron microscopy. The strands of chirally substituted PPEs display a striated structure that suggests that the whole feature is a single chirally twisted crystallite.

Journal Article↗