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1.
Int J Mol Sci ; 14(5): 10570-81, 2013 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-23698779

RESUMO

In this paper, we investigated the intra-species bacterial quorum sensing at the single cell level using a double droplet trapping system. Escherichia coli transformed to express the quorum sensing receptor protein, LasR, were encapsulated in microdroplets that were positioned adjacent to microdroplets containing the autoinducer, N-(3-oxododecanoyl)-L-homoserine lactone (OdDHL). Functional activation of the LasR protein by diffusion of the OdDHL across the droplet interface was measured by monitoring the expression of green fluorescent protein (GFP) from a LasR-dependent promoter. A threshold concentration of OdDHL was found to induce production of quorum-sensing associated GFP by E. coli. Additionally, we demonstrated that LasR-dependent activation of GFP expression was also initiated when the adjacent droplets contained single E. coli transformed with the OdDHL synthase gene, LasI, representing a simple quorum sensing circuit between two droplets.


Assuntos
Proteínas de Bactérias/metabolismo , Escherichia coli/metabolismo , Técnicas Analíticas Microfluídicas/métodos , Percepção de Quorum , Análise de Célula Única/métodos , 4-Butirolactona/análogos & derivados , 4-Butirolactona/metabolismo , Proteínas de Bactérias/genética , Escherichia coli/citologia , Escherichia coli/genética , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Homosserina/análogos & derivados , Homosserina/metabolismo , Técnicas Analíticas Microfluídicas/instrumentação , Microscopia de Fluorescência , Regiões Promotoras Genéticas/genética , Análise de Célula Única/instrumentação , Transativadores/genética , Transativadores/metabolismo , Transformação Genética
2.
J Med Chem ; 65(2): 1171-1205, 2022 01 27.
Artigo em Inglês | MEDLINE | ID: mdl-34726055

RESUMO

The allosteric regulation of pyruvate kinase M2 (PKM2) affects the switching of the PKM2 protein between the high-activity and low-activity states that allow ATP and lactate production, respectively. PKM2, in its low catalytic state (dimeric form), is chiefly active in metabolically energetic cells, including cancer cells. More recently, PKM2 has emerged as an attractive target due to its role in metabolic dysfunction and other interrelated conditions. PKM2 (dimer) activity can be inhibited by modulating PKM2 dimer-tetramer dynamics using either PKM2 inhibitors that bind at the ATP binding active site of PKM2 (dimer) or PKM2 activators that bind at the allosteric site of PKM2, thus activating PKM2 from the dimer formation to the tetrameric formation. The present perspective focuses on medicinal chemistry approaches to design and discover PKM2 inhibitors and activators and further provides a scope for the future design of compounds targeting PKM2 with better efficacy and selectivity.


Assuntos
Proteínas de Transporte/antagonistas & inibidores , Química Farmacêutica , Glicólise , Proteínas de Membrana/antagonistas & inibidores , Inibidores de Proteínas Quinases/farmacologia , Regulação Alostérica , Sítio Alostérico , Humanos , Hormônios Tireóideos , Proteínas de Ligação a Hormônio da Tireoide
3.
Lab Chip ; 10(10): 1281-5, 2010 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-20445881

RESUMO

Here we present the design, fabrication and operation of a microfluidic device to trap droplets in a large array of droplet pairs in a controlled manner with the aim of studying the transport of small molecules across the resultant surfactant bilayers formed between the droplet pairs.


Assuntos
Técnicas Analíticas Microfluídicas , Microtecnologia/métodos , Movimento (Física) , Tensoativos/química , Difusão , Fluoresceína/química , Corantes Fluorescentes/química , Peróxido de Hidrogênio/química , Cinética
4.
Org Lett ; 9(2): 195-8, 2007 Jan 18.
Artigo em Inglês | MEDLINE | ID: mdl-17217263

RESUMO

A facile synthesis of beta-functionalized gamma-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereoselective. [reaction: see text].


Assuntos
4-Butirolactona/síntese química , Furanos/química , Oxigênio/química , 4-Butirolactona/análogos & derivados , 4-Butirolactona/química , Estrutura Molecular , Estereoisomerismo
5.
Lab Chip ; 11(6): 1132-7, 2011 Mar 21.
Artigo em Inglês | MEDLINE | ID: mdl-21298160

RESUMO

A microfluidic device capable of exploiting the permeability of small molecules through polydimethylsiloxane (PDMS) has been fabricated in order to control the contents of microdroplets stored in storage wells. We demonstrate that protein precipitation and crystallization can be triggered by delivery of ethanol from a reservoir channel, thus controlling the protein solubility in microdroplets. Likewise quorum sensing in bacteria was triggered by delivery of the auto-inducer N-(3-oxododecanoyl)-l-homoserine lactone (OdDHL) through the PDMS membrane of the device.


Assuntos
Dimetilpolisiloxanos/química , Técnicas Analíticas Microfluídicas/métodos , 4-Butirolactona/análogos & derivados , 4-Butirolactona/química , Cristalização , Escherichia coli/metabolismo , Proteínas de Fluorescência Verde/metabolismo , Homosserina/análogos & derivados , Homosserina/química , Técnicas Analíticas Microfluídicas/instrumentação , Microscopia de Fluorescência , Permeabilidade , Percepção de Quorum/efeitos dos fármacos
6.
J Org Chem ; 73(12): 4476-83, 2008 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-18489153

RESUMO

The scope and limitations of a regioselective synthesis of either alpha- or beta-substituted gamma-hydroxybutenolides from 3-furfural and enones are described. The sequence features a Baylis-Hillman reaction followed by singlet oxygen oxidation with use of either an amine base or TBAF as the regioselectivity switches. Structural studies in solution on some of the resulting gamma-hydroxybutenolides are also reported.


Assuntos
Butanóis/síntese química , Oxigênio/química , Butanóis/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Estereoisomerismo
7.
J Org Chem ; 72(16): 6305-8, 2007 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-17629339

RESUMO

A facile synthesis of alpha-substituted gamma-hydroxybutenolides from 3-furfural was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The regioselectivity of this conversion was controlled by using TBAF.


Assuntos
4-Butirolactona/análogos & derivados , Química Orgânica/métodos , Fluoretos/química , Furanos/química , Oxigênio Singlete , 4-Butirolactona/química , Catálise , Modelos Químicos , Oxigênio/química , Compostos de Amônio Quaternário/química , Oxigênio Singlete/química , Estereoisomerismo
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