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1.
Angew Chem Int Ed Engl ; 56(38): 11471-11474, 2017 09 11.
Artigo em Inglês | MEDLINE | ID: mdl-28719004

RESUMO

Most alignment media for the residual dipolar coupling (RDC) based molecular structure determination of small organic compounds consist of rod-like polymers dissolved in organic solvents or of swollen cross-linked polymer gels. Thus far, the synthesis of polymer-based alignment media has been a challenging process, which is often followed by a time-consuming sample preparation. We herein propose the use of non-polymeric alignment media based on benzenetricarboxamides (BTAs), which self-assemble into rod-like supramolecules. Our newly found supramolecular lyotropic liquid crystals (LLCs) are studied in terms of their LLC properties and their suitability as alignment media in NMR spectroscopy. Scalable enantiodifferentiating properties are introduced through a sergeant-and-soldier principle by blending achiral with chiral substituted BTAs.

2.
J Biol Chem ; 285(6): 3896-3904, 2010 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-19917608

RESUMO

COX-2 (cyclooxygenase-2) is a pivotal player in inflammatory processes, and ultraviolet radiation is a known stimulus for COX-2 expression in skin cells. Here, an induction of COX-2 expression in HaCaT human keratinocytes was observed only upon exposure of cells to UVB (280-320 nm) but not to UVA radiation (320-400 nm), as demonstrated by reverse transcription-PCR and Western blotting. Prostaglandin E(2) levels were elevated in cell culture supernatants of HaCaT cells exposed to UVB. COX-2 mRNA stability was dramatically increased by UVB irradiation. Both the stabilization of COX-2 mRNA and the enhancement of COX-2 steady-state mRNA and protein levels caused by UVB were prevented both by inhibition and small interfering RNA-induced depletion of p38(MAPK), a kinase strongly activated upon exposure to UVB, suggesting p38(MAPK)-dependent mRNA stabilization as a mechanism of UVB-induced COX-2 expression. A dramatic decrease in COX-2 expression induced by UVB was elicited by small interfering RNA-based depletion of a stress-responsive mRNA stabilizing protein regulated by p38(MAPK), i.e. HuR; UVB-induced elevation of COX-2 mRNA and protein levels coincided with an accumulation of HuR in the cytoplasm and was attenuated in cells depleted of HuR. Moreover, UVB-induced generation of prostaglandin E(2) by HaCaT cells was blunted by HuR depletion, suggesting that stress kinases (such as p38(MAPK)) as well as HuR are excellent targets for approaches aiming at interfering with induction of COX-2 expression by UVB.


Assuntos
Antígenos de Superfície/metabolismo , Ciclo-Oxigenase 2/genética , Queratinócitos/efeitos da radiação , Proteínas de Ligação a RNA/metabolismo , Raios Ultravioleta , Proteínas Quinases p38 Ativadas por Mitógeno/metabolismo , Antígenos de Superfície/genética , Western Blotting , Linhagem Celular , Sobrevivência Celular/efeitos da radiação , Ciclo-Oxigenase 2/metabolismo , Citoplasma/metabolismo , Citoplasma/efeitos da radiação , Dinoprostona/metabolismo , Relação Dose-Resposta à Radiação , Proteínas ELAV , Proteína Semelhante a ELAV 1 , Regulação da Expressão Gênica/efeitos da radiação , Regulação Enzimológica da Expressão Gênica/efeitos da radiação , Humanos , Indóis/farmacologia , Queratinócitos/citologia , Queratinócitos/metabolismo , Maleimidas/farmacologia , Proteína Quinase C/antagonistas & inibidores , Proteína Quinase C/metabolismo , Interferência de RNA , Estabilidade de RNA/efeitos da radiação , Proteínas de Ligação a RNA/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Proteínas Quinases p38 Ativadas por Mitógeno/genética
3.
Chem Commun (Camb) ; 52(84): 12506-12509, 2016 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-27722553

RESUMO

Photochromic compounds like azobenzenes are widely used for the production of stimuli responsive materials. To analyse cascaded azobenzene switching inside a benzene-tricarboxamide (BTA) with three azobenzene moieties in a site-specific fashion, we used in situ irradiation NMR spectroscopy. Four photoisomers can be distinguished by their chemical shifts. Analysis of 1H, 13C and 15N shifts reveals that the configuration of one sidechain has an influence on the chemical shifts of both the other sidechains. Interconversion kinetics upon irradiation with ultraviolet (UV) light as well as molar fractions in photostationary states (PSS) were examined. Analysis of thermal fading of the different photoisomers into the ground state shows that thermal relaxation rates of all three azobenzene moieties behave as if they were independent of each other.

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