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1.
Structure ; 7(5): R91-7, 1999 May.
Artículo en Inglés | MEDLINE | ID: mdl-10378263

RESUMEN

The recently determined crystal structure of the PR65/A subunit of protein phosphatase 2A reveals the architecture of proteins containing HEAT repeats. The structural properties of this solenoid protein explain many functional characteristics and account for the involvement of solenoids as scaffold, anchoring and adaptor proteins.


Asunto(s)
Fosfoproteínas Fosfatasas/química , Conformación Proteica , Proteína Fosfatasa 2
2.
Sci Rep ; 6: 32837, 2016 09 06.
Artículo en Inglés | MEDLINE | ID: mdl-27596612

RESUMEN

The isolation and analysis of single prokaryotic cells down to 1 µm and less in size poses a special challenge and requires micro-engineered devices to handle volumes in the picoliter to nanoliter range. Here, an advanced Single-Cell Printer (SCP) was applied for automated and label-free isolation and deposition of bacterial cells encapsulated in 35 pl droplets by inkjet-like printing. To achieve this, dispenser chips to generate micro droplets have been fabricated with nozzles 20 µm in size. Further, the magnification of the optical system used for cell detection was increased. Redesign of the optical path allows for collision-free addressing of any flat substrate since no compartment protrudes below the nozzle of the dispenser chip anymore. The improved system allows for deterministic isolation of individual bacterial cells. A single-cell printing efficiency of 93% was obtained as shown by printing fluorescent labeled E. coli. A 96-well plate filled with growth medium is inoculated with single bacteria cells on average within about 8 min. Finally, individual bacterial cells from a heterogeneous sample of E. coli and E. faecalis were isolated for clonal culturing directly on agar plates in user-defined array geometry.


Asunto(s)
Técnicas de Cultivo de Célula/instrumentación , Técnicas de Cultivo de Célula/métodos , Fenómenos Fisiológicos Celulares , Separación Celular/métodos , Escherichia coli/citología , Análisis de la Célula Individual/instrumentación , Análisis de la Célula Individual/métodos , Separación Celular/instrumentación , Supervivencia Celular , Escherichia coli/fisiología , Impresión
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