62 results match your criteria: "Chevron Science Center[Affiliation]"

Introduction: Blood-based biomarkers (BBMs) can enable early detection of brain amyloid beta (Aβ) pathology in cognitively unimpaired individuals. However, the extent to which common medical conditions affect biomarker performance remains unclear.

Methods: Participants (n = 348) included individuals without cognitive impairment.

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Article Synopsis
  • A specially designed anthracene-based monomer was found to crystallize in a favorable arrangement for Diels-Alder reactions, allowing for potential linear polymer formation, as shown by single-crystal X-ray diffraction.
  • When heated above 125°C, instead of forming a polymer, the monomer underwent an unexpected intramolecular Diels-Alder reaction, confirmed by various analytical techniques.
  • This study highlights that while Schmidt's criteria predict polymerization based on crystal structure, they can be misleading in heat-induced situations, as the molecular rotation led to a different reaction pathway.
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Two NAD(P)H-biosensing probes consisting of 1,3,3-trimethyl-3H-indolium and 3-quinolinium acceptors, linked by thiophene, , and 3,4-ethylenedioxythiophene, , bridges are detailed. We synthesized probes and , replacing the thiophene connection in probe with phenyl and 2,1,3-benzothiadiazole units, respectively. Probe was prepared by substituting probe 's 3-quinolinium unit with a 1-methylquinoxalin-1-ium unit.

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Salt Effects on the Phase Behavior and Cocrystallization Kinetics of POCB-Water Mixtures.

Langmuir

February 2024

Department of Chemical Engineering, University of Pittsburgh, 940 Benedum Hall, Pittsburgh 15261, Pennsylvania, USA.

Mixtures of water with polyoxacyclobutane (POCB) have a unique phase diagram which combines liquid-liquid equilibrium (LLE) at high temperatures and cocrystallization of a POCB-hydrate at low temperatures. Such cocrystal hydrate formation is extremely rare among polymers. We report on the effects of adding NaCl salt on the phase behavior of POCB-water mixtures and the kinetics of hydrate crystallization from such mixtures.

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A series of near-infrared fluorescent probes, labeled A to E, were developed by combining electron-rich thiophene and 3,4-ethylenedioxythiophene bridges with 3-quinolinium and various electron deficient groups, enabling the sensing of NAD(P)H. Probes A and B exhibit absorptions and emissions in the near-infrared range, offering advantages such as minimal interference from autofluorescence, negligible photo impairment in cells and tissues, and exceptional tissue penetration. These probes show negligible fluorescence when NADH is not present, and their absorption maxima are at 438 nm and 470 nm, respectively.

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Pulsed dipolar EPR spectroscopy (PDS) in combination with site-directed spin labeling is a powerful tool in structural biology. However, the commonly used spin labels are conjugated to biomolecules via rather long and flexible linkers, which hampers the translation of distance distributions into biomolecular conformations. In contrast, the spin label copper(II)-nitrilotriacetic acid [Cu (NTA)] bound to two histidines (dHis) is rigid and yields narrow distance distributions, which can be more easily translated into biomolecular conformations.

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Successive High-Resolution (HO)-GCIB and C-SIMS Imaging Integrates Multi-Omics in Different Cell Types in Breast Cancer Tissue.

Anal Chem

June 2021

Department of Chemistry, Pennsylvania State University, Chemistry Building, Shortlidge Rd, University Park, Pennsylvania 16802, United States.

The temporo-spatial organization of different cells in the tumor microenvironment (TME) is the key to understanding their complex communication networks and the immune landscape that exists within compromised tissues. Multi-omics profiling of single-interacting cells in the native TME is critical for providing further information regarding the reprograming mechanisms leading to immunosuppression and tumor progression. This requires new technologies for biomolecular profiling of phenotypically heterogeneous cells on the same tissue sample.

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The neurochemical transmitter dopamine (DA) is implicated in a number of diseases states, including Parkinson's disease, schizophrenia, and drug abuse. DA terminal fields in the dorsal striatum and core region of the nucleus accumbens in the rat brain are organized as heterogeneous domains exhibiting fast and slow kinetic of DA release. The rates of dopamine release are significantly and substantially faster in the fast domains relative to the slow domains.

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A crosslinked, low pH-stable, mixed-mode cation-exchange like stationary phase made using the thiol-yne click reaction.

J Chromatogr A

May 2020

Chevron Science Center, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, United States. Electronic address:

Mixed-mode cation-exchange stationary phases are useful for the separation of mixtures containing hydrophobic, acidic, and basic molecules. To ensure that weak organic bases are protonated and carboxylic acids are neutral low pH mobile phases are required. Mixed-mode stationary phases that are stable at pH < 3 are needed.

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Two-component systems allow bacteria to respond to changes in environmental or cytosolic conditions through autophosphorylation of a histidine kinase (HK) and subsequent transfer of the phosphate group to its downstream cognate response regulator (RR). The RR then elicits a cellular response, commonly through regulation of transcription. Engineering two-component system signaling networks provides a strategy to study bacterial signaling mechanisms related to bacterial cell survival, symbiosis, and virulence, and to develop sensory devices in synthetic biology.

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Poly(propylene fumarate) (PPF) is a biodegradable polymer that has been investigated extensively over the last three decades. It has led many scientists to synthesize and fabricate a variety of PPF-based materials for biomedical applications due to its controllable mechanical properties, tunable degradation and biocompatibility. This review provides a comprehensive overview of the progress made in improving PPF synthesis, resin formulation, crosslinking, device fabrication and post polymerization modification.

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A pH-stable, crosslinked stationary phase based on the thiol-yne reaction.

J Chromatogr A

August 2019

University of Pittsburgh, Chevron Science Center, 219 Parkman Avenue, Pittsburgh, PA 15260, United States. Electronic address:

Stationary phases that can withstand extremes of pH and temperature are needed to allow a single column to accommodate a wider set of solutes and separation criteria. We used a simple multi-step process using the thiol-yne reaction following the modification of the silica surface with a thiol-containing silane. The monomers 1,4-diethynylbenzene (DEB) and 1,6-hexanedithiol were used to create a crosslinked thiol-yne (CTY) stationary phase along the surface of the thiol functionalized silica.

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A liquid chromatographic charge transfer stationary phase based on the thiol-yne reaction.

J Chromatogr A

April 2019

University of Pittsburgh, Chevron Science Center, 219 Parkman Avenue, Pittsburgh, PA 15260, United States. Electronic address:

In the process of developing a pH-stable, highly crosslinked stationary phase using the thiol-yne reaction, a new charge transfer stationary phase was discovered. The first step in the preparation of the crosslinked phase is to attach 1,4-diethynylbenzene (DEB) to thiol functionalized silica particles using the thiol-yne reaction. Upon preparation of that phase, we noticed that the color of the particles was different when the modified particles were wet with aromatic solvents in comparison to wetting with nonaromatic or aqueous solvents.

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Multiplicative On-Column Solute Focusing Using Spatially Dependent Temperature Programming for Capillary HPLC.

Anal Chem

February 2019

Department of Chemistry, Chevron Science Center , University of Pittsburgh, Pittsburgh , Pennsylvania 15260 , United States.

The benefits of capillary liquid chromatography columns are truly realized when small, limited sample volumes require signal enhancement, but the available sample volume does not permit on-column focusing during injection onto a larger column. This dilemma is common when samples are naturally small or precious (such as in biological, forensic, art, and archeological investigations) and analyte concentrations are low. Signal enhancement by solvent-based focusing is effective with capillary columns, but it is limited to a single band-compression step and can only be achieved at the inlet.

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Predicting retention and enthalpy allows for the simulation and optimization of advanced chromatographic techniques including gradient separations, temperature-assisted solute focusing, multidimensional liquid chromatography, and solvent focusing. In this paper we explore the fits of three expressions for retention as a function of mobile phase composition and temperature to retention data of 101 small molecules in reversed phase liquid chromatography. The three retention equations investigated are those by Neue and Kuss (NK) and two different equations by Pappa-Louisi et al.

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Over-expression of the Hsp70 molecular chaperone prevents protein aggregation and ameliorates neurodegenerative disease phenotypes in model systems. We identified an Hsp70 activator, MAL1-271, that reduces α-synuclein aggregation in a Parkinson's Disease model. We now report that MAL1-271 directly increases the ATPase activity of a eukaryotic Hsp70.

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Electrokinetic infusions into hydrogels and brain tissue: Control of direction and magnitude of solute delivery.

J Neurosci Methods

January 2019

Department of Chemistry, 219 Parkman Avenue, Chevron Science Center, University of Pittsburgh, Pittsburgh, Pennsylvania 15213 USA. Electronic address:

Background: Delivering solutes to a particular region of the brain is currently achieved by iontophoresis for very small volumes and by diffusion from a microdialysis probe for larger volumes. There is a need to deliver solutes to particular areas with more control than is possible with existing methods.

New Method: Electrokinetic infusions of solutes were performed into hydrogels and organotypic hippocampal slice cultures.

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Polymer-Doped Molten Salt Mixtures as a New Concept for Electrolyte Systems in Dye-Sensitized Solar Cells.

ACS Omega

October 2017

Applied Physical Chemistry, Center for Molecular Devices, Department of Chemistry, School of Chemical Science and Engineering, KTH Royal Institute of Technology, SE-100 44 Stockholm, Sweden.

A conceptually new polymer electrolyte for dye-sensitized solar cells is reported and investigated. The benefits of using this type of electrolyte based on ionic liquid mixtures (ILMs) and room temperature ionic liquids are highlighted. Impedance spectroscopy and transient electron measurements have been used to elucidate the background of the photovoltaic performance.

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Specific Acetylation Patterns of H2A.Z Form Transient Interactions with the BPTF Bromodomain.

Biochemistry

September 2017

Department of Chemistry, University of Minnesota, 207 Pleasant Street Southeast, Minneapolis, Minnesota 55455, United States.

Post-translational lysine acetylation of histone tails affects both chromatin accessibility and recruitment of multifunctional bromodomain-containing proteins for modulating transcription. The bromodomain- and PHD finger-containing transcription factor (BPTF) regulates transcription but has also been implicated in high gene expression levels in a variety of cancers. In this report, the histone variant H2A.

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Direct Nanofabrication Using DNA Nanostructure.

Methods Mol Biol

January 2018

Department of Chemistry, University of Pittsburgh, 201 Eberly Hall, Chevron Science Center, 219 Parkman Avenue, Pittsburgh, PA, 15260, USA.

Recent advances in DNA nanotechnology make it possible to fabricate arbitrarily shaped 1D, 2D, and 3D DNA nanostructures through controlled folding and/or hierarchical assembly of up to several thousands of unique sequenced DNA strands. Both individual DNA nanostructures and their assembly can be made with almost arbitrarily shaped patterns at a theoretical resolution down to 2 nm. Furthermore, the deposition of DNA nanostructures on a substrate can be made with precise control of their location and orientation, making them ideal templates for bottom-up nanofabrication.

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DNA charge transfer: Hot holes break the speed limit.

Nat Chem

October 2016

Department of Chemistry, University of Pittsburgh, Dietrich School of Arts and Sciences, Chevron Science Center, 219 Parkman Avenue, Pittsburgh, Pennsylvania 15260, USA.

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Red-Shifting Azobenzene Photoswitches for in Vivo Use.

Acc Chem Res

October 2015

Department of Chemistry, University of Toronto, 80 St. George St., Toronto, ON M5S 3H6, Canada.

Recently, there has been a great deal of interest in using the photoisomerization of azobenzene compounds to control specific biological targets in vivo. These azo compounds can be used as research tools or, in principle, could act as optically controlled drugs. Such "photopharmaceuticals" offer the prospect of targeted drug action and an unprecedented degree of temporal control.

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Glutamine and Asparagine Side Chain Hyperconjugation-Induced Structurally Sensitive Vibrations.

J Phys Chem B

October 2015

Department of Chemistry, University of Pittsburgh , 219 Parkman Avenue, Chevron Science Center, Pittsburgh, Pennsylvania 15260, United States.

We identified vibrational spectral marker bands that sensitively report on the side chain structures of glutamine (Gln) and asparagine (Asn). Density functional theory (DFT) calculations indicate that the Amide III(P) (AmIII(P)) vibrations of Gln and Asn depend cosinusoidally on their side chain OCCC dihedral angles (the χ3 and χ2 angles of Gln and Asn, respectively). We use UV resonance Raman (UVRR) and visible Raman spectroscopy to experimentally correlate the AmIII(P) Raman band frequency to the primary amide OCCC dihedral angle.

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Raman hyperspectral imaging spectrometer utilizing crystalline colloidal array photonic crystal diffraction.

Appl Spectrosc

May 2015

University of Pittsburgh, Department of Chemistry, 219 Parkman Avenue, Chevron Science Center, Room 701, Pittsburgh, PA 15260 USA.

We fabricated a novel hyperspectral Raman imaging spectrometer that, for the first time, uses a photonic-crystal wavelength-selecting device to select a narrow-wavelength spectral interval. The photonic crystal consists of an array of highly charged, monodisperse polystyrene particles that self-assemble into a face-centered cubic crystal. The photonic crystal Bragg-diffracts a narrow spectral interval that can be tuned by altering the incident angle of collimated Raman scattered light.

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Fluorous mixture synthesis minimizes the effort to synthesize small-molecule libraries by labelling the molecules rather than the reaction vessels. Reactants are labelled with fluorinated tags and products can later be demixed based on the fluorine content. A limit in the number of available tags can be overcome by using binary encoding so that a total of four tags can label uniquely a library of 16 compounds.

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