Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
Tipo de estudio
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
STAR Protoc ; 5(1): 102930, 2024 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-38430520

RESUMEN

RNA-DNA covalent hybrids (RDHs) are widely employed in biology. Although RDHs can be manufactured, the synthesis of molecules longer than 120 nucleotides is challenging. Here, we present a protocol for the generation and purification of high-grade purified high-molecular-weight 5'-RNA-DNA-3' hybrids. We describe steps for preparing oligos and buffers, ligation reaction, and high-performance liquid chromatography-based RDH purification. This protocol is executable in standard molecular biology laboratories.


Asunto(s)
ADN , ARN , ADN/genética , ARN Ligasa (ATP)
2.
ACS Chem Biol ; 15(1): 179-188, 2020 01 17.
Artículo en Inglés | MEDLINE | ID: mdl-31874027

RESUMEN

Lactose intolerance is a common digestive disorder that affects a large proportion of the adult human population. The severity of the symptoms is highly variable, depending on the susceptibility to the sugar and the amount digested. For that reason, enzymes that can be used for the production of lactose-free milk and milk derivatives have acquired singular biotechnological importance. One such case is Thermotoga maritima ß-galactosidase (TmLac). Here, we report the cryo-EM structure of TmLac at 2.0 Å resolution. The protein features a newly solved domain at its C-terminus, characteristic of the genus Thermotoga, which promotes a peculiar octameric arrangement. We have assessed the constraints imposed by the quaternary protein structure on the construction of hybrid versions of this GH2 enzyme. Carbohydrate binding modules (CBM) from the CBM2 and CBM9 families have been added at either the amino or carboxy terminus, and the structural and functional effects of such modifications have been analyzed. The results provide a basis for the rational design of hybrid enzymes that can be efficiently attached to different solid supports.


Asunto(s)
Proteínas Bacterianas/química , Microscopía por Crioelectrón/métodos , Estructura Cuaternaria de Proteína , Thermotoga maritima/enzimología , beta-Galactosidasa/química , Aminas/química , Secuencia de Aminoácidos , Proteínas Bacterianas/metabolismo , Carbohidratos/química , Ácidos Carboxílicos/química , Dominio Catalítico , Cristalografía por Rayos X , Enzimas Inmovilizadas/química , Enzimas Inmovilizadas/metabolismo , Humanos , Modelos Moleculares , Ingeniería de Proteínas/métodos , Estabilidad Proteica , Solventes/química , Relación Estructura-Actividad , Especificidad por Sustrato , beta-Galactosidasa/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA