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1.
Biochim Biophys Acta Biomembr ; 1866(5): 184331, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38718958

RESUMEN

The causative genes for neurodegenerative polyglutamine (polyQ) diseases produce homopolymeric polyglutamine (polyQ), polyserine (polyS), polyalanine (polyA), polycysteine (polyC), and polyleucine (polyL) sequences by repeat-associated non-AUG (RAN) translation. The cytotoxicity of the intracellular polyQ and RAN products has been extensively investigated. However, little is known about the toxicity of the extracellular polyQ and RAN products on the membranes of viable cells. Because polyQ aggregates induce a deflated morphology of a model membrane, we hypothesized that extracellular polyQ and RAN products might affect the membrane properties of viable cells. In this study, we demonstrated that exogenous polyS fibrils but not polyS or polyQ non-fibril aggregates altered the thermal phase transition behavior of a model membrane composed of a phosphatidylcholine bilayer using differential scanning calorimetry. PolyS fibrils induced morphological changes in viable red blood cells (RBCs). However, both polyS and polyQ non-fibril aggregates had no effects on RBCs. These results highlight the possibility that extracellular fibrils generated from RAN products may alter the properties of neuronal cell membranes, which may contribute to changes in the brain pathology.


Asunto(s)
Eritrocitos , Liposomas , Péptidos , Fosfatidilcolinas , Eritrocitos/efectos de los fármacos , Eritrocitos/metabolismo , Fosfatidilcolinas/química , Humanos , Liposomas/química , Péptidos/química , Péptidos/farmacología , Membrana Celular/metabolismo , Membrana Celular/efectos de los fármacos , Membrana Celular/química , Transición de Fase , Membrana Dobles de Lípidos/química , Membrana Dobles de Lípidos/metabolismo
2.
Biochem Cell Biol ; 102(3): 238-251, 2024 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-38408323

RESUMEN

Insects are the largest group of animals when it comes to the number and diversity of species. Yet, with the exception of Drosophila, no information is currently available on the primary structure of their sperm nuclear basic proteins (SNBPs). This paper represents the first attempt in this regard and provides information about six species of Neoptera: Poecillimon thessalicus, Graptosaltria nigrofuscata, Apis mellifera, Nasonia vitripennis, Parachauliodes continentalis, and Tribolium castaneum. The SNBPs of these species were characterized by acetic acid urea gel electrophoresis (AU-PAGE) and high-performance liquid chromatography fractionated. Protein sequencing was obtained using a combination of mass spectrometry sequencing, Edman N-terminal degradation sequencing and genome mining. While the SNBPs of several of these species exhibit a canonical arginine-rich protamine nature, a few of them exhibit a protamine-like composition. They appear to be the products of extensive cleavage processing from a precursor protein which are sometimes further processed by other post-translational modifications that are likely involved in the chromatin transitions observed during spermiogenesis in these organisms.


Asunto(s)
Secuencia de Aminoácidos , Protaminas , Animales , Masculino , Protaminas/metabolismo , Protaminas/química , Proteínas Nucleares/metabolismo , Proteínas Nucleares/genética , Proteínas de Insectos/metabolismo , Proteínas de Insectos/química , Proteínas de Insectos/genética , Insectos/metabolismo , Datos de Secuencia Molecular , Espermatozoides/metabolismo
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