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1.
Pharmaceuticals (Basel) ; 17(6)2024 Jun 16.
Artículo en Inglés | MEDLINE | ID: mdl-38931455

RESUMEN

The COVID-19 pandemic, caused by infection with the SARS-CoV-2 virus, is associated with cognitive impairment and Alzheimer's disease (AD) progression. Once it enters the brain, the SARS-CoV-2 virus stimulates accumulation of amyloids in the brain that are highly toxic to neural cells. These amyloids may trigger neurological symptoms in COVID-19. The meningeal lymphatic vessels (MLVs) play an important role in removal of toxins and mediate viral drainage from the brain. MLVs are considered a promising target to prevent COVID-19-exacerbated dementia. However, there are limited methods for augmentation of MLV function. This review highlights new discoveries in the field of COVID-19-mediated amyloid accumulation in the brain associated with the neurological symptoms and the development of promising strategies to stimulate clearance of amyloids from the brain through lymphatic and other pathways. These strategies are based on innovative methods of treating brain dysfunction induced by COVID-19 infection, including the use of photobiomodulation, plasmalogens, and medicinal herbs, which offer hope for addressing the challenges posed by the SARS-CoV-2 virus.

2.
Methods Mol Biol ; 2118: 213-225, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32152982

RESUMEN

Direct immobilization of functional proteins on gold nanoparticles (AuNPs) affects their structure and function. Changes may vary widely and range from strong inhibition to the enhancement of protein function. More often though the outcome of direct protein immobilization results in protein misfolding and the loss of protein activity. Additional complications arise when the protein being immobilized is a zymogen which requires and relies on additional protein-protein interactions to exert its function. Here we describe molecular design of a glutathione-S-transferase-Staphylokinase fusion protein (GST-SAK) and its conjugation to AuNPs. The multivalent AuNP-(GST-SAK)n complexes generated show plasminogen activation activity in vitro. The methods described are transferable and could be adapted for conjugation and functional analysis of other plasminogen activators, thrombolytic preparations or other functional enzymes.


Asunto(s)
Glutatión Transferasa/genética , Oro/química , Metaloendopeptidasas/genética , Activadores Plasminogénicos/farmacología , Proteínas Recombinantes/farmacología , Enzimas Inmovilizadas/química , Enzimas Inmovilizadas/farmacología , Fibrinógeno/metabolismo , Glutatión Transferasa/química , Humanos , Nanopartículas del Metal , Metaloendopeptidasas/química , Modelos Moleculares , Activadores Plasminogénicos/química , Conformación Proteica , Pliegue de Proteína , Proteínas Recombinantes/química
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