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1.
Anal Chem ; 93(31): 10850-10861, 2021 08 10.
Artículo en Inglés | MEDLINE | ID: mdl-34320311

RESUMEN

We describe a mass spectrometry (MS) analytical platform resulting from the novel integration of acoustic droplet ejection (ADE) technology, an open-port interface (OPI), and electrospray ionization (ESI)-MS that creates a transformative system enabling high-speed sampling and label-free analysis. The ADE technology delivers nanoliter droplets in a touchless manner with high speed, precision, and accuracy. Subsequent sample dilution within the OPI, in concert with the capabilities of modern ESI-MS, eliminates the laborious sample preparation and method development required in current approaches. This platform is applied to a variety of experiments, including high-throughput (HT) pharmacology screening, label-free in situ enzyme kinetics, in vitro absorption, distribution, metabolism, elimination, pharmacokinetic and biomarker analysis, and HT parallel medicinal chemistry.


Asunto(s)
Ensayos Analíticos de Alto Rendimiento , Espectrometría de Masa por Ionización de Electrospray , Acústica
2.
Structure ; 24(4): 631-640, 2016 Apr 05.
Artículo en Inglés | MEDLINE | ID: mdl-26996959

RESUMEN

X-ray free-electron lasers (XFELs) provide very intense X-ray pulses suitable for macromolecular crystallography. Each X-ray pulse typically lasts for tens of femtoseconds and the interval between pulses is many orders of magnitude longer. Here we describe two novel acoustic injection systems that use focused sound waves to eject picoliter to nanoliter crystal-containing droplets out of microplates and into the X-ray pulse from which diffraction data are collected. The on-demand droplet delivery is synchronized to the XFEL pulse scheme, resulting in X-ray pulses intersecting up to 88% of the droplets. We tested several types of samples in a range of crystallization conditions, wherein the overall crystal hit ratio (e.g., fraction of images with observable diffraction patterns) is a function of the microcrystal slurry concentration. We report crystal structures from lysozyme, thermolysin, and stachydrine demethylase (Stc2). Additional samples were screened to demonstrate that these methods can be applied to rare samples.


Asunto(s)
Cristalografía por Rayos X/instrumentación , Enzimas/química , Acústica , Cristalografía por Rayos X/métodos , Modelos Moleculares , Muramidasa/química , Conformación Proteica , Termolisina/química
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