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1.
Microsc Microanal ; 29(Supplement_1): 1044-1045, 2023 Jul 22.
Artículo en Inglés | MEDLINE | ID: mdl-37613304
2.
Nat Commun ; 11(1): 2563, 2020 05 22.
Artículo en Inglés | MEDLINE | ID: mdl-32444637

RESUMEN

The increasing demand for cryo-electron microscopy (cryo-EM) reveals drawbacks in current sample preparation protocols, such as sample waste and lack of reproducibility. Here, we present several technical developments that provide efficient sample preparation for cryo-EM studies. Pin printing substantially reduces sample waste by depositing only a sub-nanoliter volume of sample on the carrier surface. Sample evaporation is mitigated by dewpoint control feedback loops. The deposited sample is vitrified by jets of cryogen followed by submersion into a cryogen bath. Because the cryogen jets cool the sample from the center, premounted autogrids can be used and loaded directly into automated cryo-EMs. We integrated these steps into a single device, named VitroJet. The device's performance was validated by resolving four standard proteins (apoferritin, GroEL, worm hemoglobin, beta-galactosidase) to ~3 Å resolution using a 200-kV electron microscope. The VitroJet offers a promising solution for improved automated sample preparation in cryo-EM studies.


Asunto(s)
Impresión Tridimensional , Proteínas/ultraestructura , Manejo de Especímenes/métodos , Microscopía por Crioelectrón , Impresión Tridimensional/instrumentación , Proteínas/química , Reproducibilidad de los Resultados , Imagen Individual de Molécula , Manejo de Especímenes/instrumentación
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