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1.
ACS Comb Sci ; 22(3): 156-164, 2020 03 09.
Artículo en Inglés | MEDLINE | ID: mdl-32027120

RESUMEN

On the basis of computational design, a focused one-bead one-compound library has been prepared on microparticle-encoded PEGA1900 beads consisting of small tripeptides with a triazole-capped N-terminal. The library was screened towards a double point-mutated version of the human FKBP12 protein, known as the destabilizing domain (DD). Inspired by the decoded library hits, unnatural peptide structures were screened in a novel on-bead assay, which was useful for a rapid structure evaluation prior to off-bead resynthesis. Subsequently, a series of 19 compounds were prepared and tested using a competitive fluorescence polarization assay, which led to the discovery of peptide ligands with low micromolar binding affinity towards the DD. The methodology represents a rapid approach for identification of a novel structure scaffold, where the screening and initial structure refinement was accomplished using small quantities of library building blocks.


Asunto(s)
Técnicas Químicas Combinatorias , Péptidos/química , Proteína 1A de Unión a Tacrolimus/química , Sitios de Unión , Humanos , Modelos Moleculares , Estructura Molecular
2.
Plant Cell ; 28(6): 1328-42, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27268428

RESUMEN

MAP kinase (MPK) cascades in Arabidopsis thaliana and other vascular plants are activated by developmental cues, abiotic stress, and pathogen infection. Much less is known of MPK functions in nonvascular land plants such as the moss Physcomitrella patens Here, we provide evidence for a signaling pathway in P. patens required for immunity triggered by pathogen associated molecular patterns (PAMPs). This pathway induces rapid growth inhibition, a novel fluorescence burst, cell wall depositions, and accumulation of defense-related transcripts. Two P. patens MPKs (MPK4a and MPK4b) are phosphorylated and activated in response to PAMPs. This activation in response to the fungal PAMP chitin requires a chitin receptor and one or more MAP kinase kinase kinases and MAP kinase kinases. Knockout lines of MPK4a appear wild type but have increased susceptibility to the pathogenic fungi Botrytis cinerea and Alternaria brassisicola Both PAMPs and osmotic stress activate some of the same MPKs in Arabidopsis. In contrast, abscisic acid treatment or osmotic stress of P. patens does not activate MPK4a or any other MPK, but activates at least one SnRK2 kinase. Signaling via MPK4a may therefore be specific to immunity, and the moss relies on other pathways to respond to osmotic stress.


Asunto(s)
Bryopsida/inmunología , Bryopsida/metabolismo , Regulación de la Expresión Génica de las Plantas/fisiología , Inmunidad Innata/fisiología , Alternaria/inmunología , Alternaria/patogenicidad , Arabidopsis/efectos de los fármacos , Arabidopsis/inmunología , Arabidopsis/metabolismo , Arabidopsis/microbiología , Botrytis/inmunología , Botrytis/patogenicidad , Bryopsida/efectos de los fármacos , Bryopsida/microbiología , Regulación de la Expresión Génica de las Plantas/efectos de los fármacos , Regulación de la Expresión Génica de las Plantas/genética , Inmunidad Innata/genética , Presión Osmótica/efectos de los fármacos , Moléculas de Patrón Molecular Asociado a Patógenos/farmacología , Fosforilación/efectos de los fármacos , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo
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