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1.
J Proteomics ; 301: 105191, 2024 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-38697285

RESUMO

Cystic echinococcosis is a zoonotic disease resulting from infection caused by the larval stage of Echinococcus granulosus. This study aimed to assess the specific proteins that are potential candidates for the development of a vaccine against E. granulosus. The data-independent acquisition approach was employed to identify differentially expressed proteins (DEPs) in E. granulosus samples. The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis was employed to identify several noteworthy proteins. Results: The DEPs in E. granulosus samples were identified (245 pericystic wall vs. parasite-free yellowish granuloma (PYG, 1725 PY vs. PYG, 2274 PN vs. PYG). Further examination of these distinct proteins revealed their predominant enrichment in metabolic pathways, amyotrophic lateral sclerosis, and neurodegeneration-associated pathways. Notably, among these DEPs, SH3BGRL, MST1, TAGLN2, FABP5, UBE2V2, and RARRES2 exhibited significantly higher expression levels in the PYG group compared with the PY group (P < 0.05). The findings may contribute to the understanding of the pathological mechanisms underlying echinococcosis, providing valuable insights into the development of more effective diagnostic tools, treatment modalities, and preventive strategies. SIGNIFICANCE: CE is a major public health hazard in the western regions of China, Central Asia, South America, the Mediterranean countries, and eastern Africa. Echinococcus granulosus is responsible for zoonotic disease through infection Our analysis focuses on the proteins in various samples by data-dependent acquisition (DIA) for proteomic analysis. The importance of this research is to develop new strategies and targets to protect against E. granulosus infections in humans.


Assuntos
Echinococcus granulosus , Proteômica , Proteômica/métodos , Humanos , Echinococcus granulosus/metabolismo , Animais , Proteínas de Helminto/metabolismo , Proteínas de Helminto/análise , Equinococose Hepática/metabolismo , Equinococose Hepática/parasitologia , Proteoma/análise , Proteoma/metabolismo
2.
J Zhejiang Univ Sci ; 5(1): 81-5, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-14663857

RESUMO

This paper presents a method for robust tolerance design in terms of Process Capability Indices (PCI). The component tolerance and the suitable manufacturing processes can be selected based on the real manufacturing context. The robustness of design feasibility under the effect of uncertainties is also discussed. A comparison between the results obtained by the proposed model and other methods indicates that robust and reliable tolerance can be obtained.


Assuntos
Algoritmos , Desenho Assistido por Computador , Desenho de Equipamento/métodos , Análise de Falha de Equipamento/métodos , Modelos Estatísticos , Benchmarking/métodos , Simulação por Computador , Controle de Qualidade
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