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1.
Inflammopharmacology ; 30(5): 1479-1491, 2022 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-35635676

RESUMO

COVID-19 is one of the viral diseases that has caused many deaths and financial losses to humans. Using the available information, this virus appears to activate the host cell-death mechanism through Calpain activation. Calpain inhibition can stop its downstream cascade reactions that cause cell death. Given the main roles of Calpain in the entry and pathogenicity of the SARS-CoV-2, its inhibition can be effective in controlling the COVID-19. This review describes how the virus activates Calpain by altering calcium flow. When Calpain was activated, the virus can enter the target cell. Subsequently, many complications of the disease, such as inflammation, cytokine storm and pulmonary fibrosis, are caused by virus-activated Calpain function. Calpain inhibitors appear to be a potential drug to control the disease and prevent death from COVID-19.


Assuntos
Tratamento Farmacológico da COVID-19 , Cálcio , Calpaína/metabolismo , Síndrome da Liberação de Citocina , Humanos , SARS-CoV-2
2.
J Med Life ; 12(2): 184-191, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31406522

RESUMO

Hypoparathyroidism is a rare endocrine disease which is characterized by the deficiency of serum calcium levels. RhPTH is prescribed as a therapy for the management of refractory hypoparathyroidism. The aim of this study is to investigate 32 signal peptides of gram-negative bacterial origin and evaluate their potential for efficient secretion of recombinant human PTH (1-84)In E.coli to obtain higher expression of recombinant PTH in bacterial systems by using this fusion partner. SignalP and ProtParam servers were employed to predict the presence and location of signal peptide cleavage sites in protein sequence and computation of various physical and chemical parameters of protein respectively. Also, SOLpro server was applied for prediction of the protein solubility. Then ProtComp and SecretomeP online servers were employed to determine protein location. The evaluations showed that theoretically two signal peptides Lipopolysaccharide export system protein LptA (lptA) and Periplasmic pH-dependent serine endoprotease DegQ (degQ) are the most appropriate signal peptides examined. Due to the lack of post-translational modification in PTH, its periplasmic expression has preferences. Based on the results of this study, using bioinformatics and reliable servers signal peptides with appropriate secretory potential can be obtained which lead to the highest expression level.


Assuntos
Biologia Computacional/métodos , Escherichia coli/metabolismo , Hormônio Paratireóideo/metabolismo , Periplasma/metabolismo , Sinais Direcionadores de Proteínas , Sequência de Aminoácidos , Simulação por Computador , Proteínas de Escherichia coli/metabolismo , Humanos , Solubilidade
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