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1.
Angew Chem Int Ed Engl ; 61(49): e202211570, 2022 Dec 05.
Artigo em Inglês | MEDLINE | ID: mdl-36216781

RESUMO

Lithium-sulfur batteries (LSBs) are still limited by the shuttle of lithium polysulfides (LiPS) and the slow Li-S reaction. Herein, we demonstrate that when using cobalt sulfide as a catalytic additive, an external magnetic field generated by a permanent magnet can significantly improve the LiPS adsorption ability and the Li-S reaction kinetics. More specifically, the results show both experimentally and theoretically how an electron spin polarization of Co ions reduces electron repulsion and enhances the degree of orbital hybridization, thus resulting in LSBs with unprecedented performance and stability. Under an external magnetic field, LSBs with 0.0084 % per cycle decay rate at 2 C during 8150 cycles are produced. Overall, this work not only demonstrates an effective strategy to promote LiPS adsorption and electrochemical conversion in LSBs at no additional energy cost but also enriches the application of the spin effect in the electrocatalysis fields.

4.
Huan Jing Ke Xue ; 39(9): 4026-4033, 2018 Sep 08.
Artigo em Chinês | MEDLINE | ID: mdl-30188042

RESUMO

Heavy pollution events frequently occur during fall and winter seasons in northern areas. In order to understand the characteristics and chemical composition of PM2.5 during heavy pollution in winter in Liaocheng City, ambient PM2.5 samples were collected between January 7-11,2016. Mass concentration, water-soluble ions, carbonaceous species, and elements were analyzed, as well as the causes of pollution. Results showed that PM2.5 mass concentration was 238.3 µg·m-3 with the trend clearly that of an inverted V; this concentration represents exceedance of the National Ambient Air Quality Standard (GB 3095-2012) by more than 2.2 times. NO3-, SO42-, and NH4+(SNA)were the main water-soluble ions. As pollution increased or decreased, NH4+, SO42-, NO3-, and Cl- exhibited the same trend, which contrasted with that of Ca2+. During the peak of pollution, NH4+, NO3-, and SO42- concentrations were 48.96, 68.45, and 80.55 µg·m-3, with these representing levels 6.29, 7.31, and 7.84 times those of the initial stage, respectively. During the pollution event, OC and EC concentration variation ranges were 20.8-60.2 µg·m-3, and 3.0-7.5 µg·m-3, respectively. The concentration of OC was significantly higher than that of EC and the variation amplitude was significantly larger. During the event, the mass concentrations of 27 inorganic elements on each day were 10.2, 22.4, 16.0, 19.6, and 8.2 µg·m-3, respectively. Enrichment factors (EF) of all elements were less than 10, indicating lack of enrichment and showing that sources were mainly natural. PM2.5 mass concentration reconstruction results showed that organic matter (OM), SO42-, and NO3- were major components, followed by NH4+, crustal material, and other ions. EC and trace element content was relatively low. As PM2.5 pollution worsened, secondary inorganic salt (NH4+, SO42-, NO3-) concentrations and proportions increased, OM concentration increased but its proportion decreased, while crustal material concentration and proportion both decreased, showing that secondary inorganic conversion was the main cause of this pollution event, mainly driven by coal and motor vehicle emissions.

5.
FEBS Lett ; 589(13): 1437-43, 2015 Jun 04.
Artigo em Inglês | MEDLINE | ID: mdl-25935522

RESUMO

PTPRZ1-MET (ZM) proteins are a group of fusion proteins identified in human gliomas by high-throughput transcriptome sequencing. ZM fusions are associated with poor prognosis in afflicted glioma patients and mediate oncogenic effects in assays. In this study, we show that ZM-carrying patients have increased hepatocyte growth factor receptor (MET) mRNA expression levels induced by fusion with receptor-type tyrosine-protein phosphatase zeta (PTPRZ1). Furthermore, ZM fusions preserve fundamental properties of wild-type MET with respect to processing and dimerization, and enhance phosphorylation in an hepatocyte growth factor (HGF)-dependent and independent manner. Our findings suggest that ZM induces gliomas through elevated expression and phosphorylation of the MET oncoprotein.


Assuntos
Regulação Neoplásica da Expressão Gênica , Proteínas de Fusão Oncogênica/genética , Proteínas Proto-Oncogênicas c-met/genética , Proteínas Tirosina Fosfatases Classe 5 Semelhantes a Receptores/genética , Western Blotting , Células HEK293 , Fator de Crescimento de Hepatócito/farmacologia , Humanos , Proteínas de Fusão Oncogênica/química , Proteínas de Fusão Oncogênica/metabolismo , Fosforilação/efeitos dos fármacos , Multimerização Proteica , Proteínas Proto-Oncogênicas c-met/química , Proteínas Proto-Oncogênicas c-met/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Proteínas Tirosina Fosfatases Classe 5 Semelhantes a Receptores/química , Proteínas Tirosina Fosfatases Classe 5 Semelhantes a Receptores/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa
6.
Genome Res ; 24(11): 1765-73, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25135958

RESUMO

Studies of gene rearrangements and the consequent oncogenic fusion proteins have laid the foundation for targeted cancer therapy. To identify oncogenic fusions associated with glioma progression, we catalogued fusion transcripts by RNA-seq of 272 gliomas. Fusion transcripts were more frequently found in high-grade gliomas, in the classical subtype of gliomas, and in gliomas treated with radiation/temozolomide. Sixty-seven in-frame fusion transcripts were identified, including three recurrent fusion transcripts: FGFR3-TACC3, RNF213-SLC26A11, and PTPRZ1-MET (ZM). Interestingly, the ZM fusion was found only in grade III astrocytomas (1/13; 7.7%) or secondary GBMs (sGBMs, 3/20; 15.0%). In an independent cohort of sGBMs, the ZM fusion was found in three of 20 (15%) specimens. Genomic analysis revealed that the fusion arose from translocation events involving introns 3 or 8 of PTPRZ and intron 1 of MET. ZM fusion transcripts were found in GBMs irrespective of isocitrate dehydrogenase 1 (IDH1) mutation status. sGBMs harboring ZM fusion showed higher expression of genes required for PIK3CA signaling and lowered expression of genes that suppressed RB1 or TP53 function. Expression of the ZM fusion was mutually exclusive with EGFR overexpression in sGBMs. Exogenous expression of the ZM fusion in the U87MG glioblastoma line enhanced cell migration and invasion. Clinically, patients afflicted with ZM fusion harboring glioblastomas survived poorly relative to those afflicted with non-ZM-harboring sGBMs (P < 0.001). Our study profiles the shifting RNA landscape of gliomas during progression and reveled ZM as a novel, recurrent fusion transcript in sGBMs.


Assuntos
Neoplasias Encefálicas/genética , Glioblastoma/genética , Glioma/genética , Proteínas de Fusão Oncogênica/genética , Proteínas Proto-Oncogênicas c-met/genética , Proteínas Tirosina Fosfatases Classe 5 Semelhantes a Receptores/genética , Adolescente , Adulto , Idoso , Antineoplásicos Alquilantes , Western Blotting , Neoplasias Encefálicas/patologia , Neoplasias Encefálicas/secundário , Linhagem Celular Tumoral , Quimiorradioterapia , Dacarbazina/análogos & derivados , Dacarbazina/uso terapêutico , Feminino , Regulação Neoplásica da Expressão Gênica , Glioblastoma/secundário , Glioma/patologia , Glioma/terapia , Células HEK293 , Humanos , Íntrons/genética , Masculino , Pessoa de Meia-Idade , Proteínas de Fusão Oncogênica/metabolismo , Proteínas Proto-Oncogênicas c-met/metabolismo , Proteínas Tirosina Fosfatases Classe 5 Semelhantes a Receptores/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Análise de Sequência de RNA , Temozolomida , Translocação Genética , Adulto Jovem
7.
Acta Crystallogr Sect E Struct Rep Online ; 68(Pt 7): o2109, 2012 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-22798786

RESUMO

The title compound, C(13)H(13)ClN(2)O(3), was synthesized in the course of the search for novel bioactive pyrimidine derivatives. The C-O-C angle at the phen-oxy O atom is widened to 119.87 (18)°. The dihedral angle between the pyrimidine and benzene rings is 64.2 (3)°.

8.
Opt Lett ; 36(5): 648-50, 2011 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-21368936

RESUMO

Using numerical simulation, we have studied in detail vacuum electron acceleration driven by two crossed Airy beams with identical characteristics except for opposite accelerating directions. An electron injected along the longitudinal central axis is only affected by the combined longitudinal electric field. In addition, a suitable crossed Airy beams scheme is more beneficial to the energy gain of an electron than the single Airy beam acceleration scheme [Opt. Lett. 35, 3258 (2010)]. Meanwhile, the cross angle, the injection energy of the electron, and the initial phase of the Airy beams play significant roles in the energy gain of the electron.

9.
J Virol ; 81(2): 954-63, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17079302

RESUMO

Most adenoviruses bind to the coxsackie- and adenovirus receptor (CAR). Surprisingly, CAR is not expressed apically on polarized cells and is thus not easily available to viruses. Consequently, alternative mechanisms for entry of coxsackievirus and adenovirus into cells have been suggested. We have found that tear fluid promotes adenovirus infection, and we have identified human lactoferrin (HLf) as the tear fluid component responsible for this effect. HLf alone was found to promote binding of adenovirus to epithelial cells in a dose-dependent manner and also infection of epithelial cells by adenovirus. HLf was also found to promote gene delivery from an adenovirus-based vector. The mechanism takes place at the binding stage and functions independently of CAR. Thus, we have identified a novel binding mechanism whereby adenovirus hijacks HLf, a component of the innate immune system, and uses it as a bridge for attachment to host cells.


Assuntos
Adenovírus Humanos/patogenicidade , Células Epiteliais/virologia , Lactoferrina/metabolismo , Receptores Virais/metabolismo , Lágrimas/química , Adenovírus Humanos/classificação , Adenovírus Humanos/metabolismo , Linhagem Celular Tumoral , Proteína de Membrana Semelhante a Receptor de Coxsackie e Adenovirus , Humanos , Especificidade da Espécie
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