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Nanoliter Dispensing Method by Degassed Poly(dimethylsiloxane) Microchannels and Its Application in Protein Crystallization

机译:脱气聚二甲基硅氧烷微通道的纳升分配方法及其在蛋白质结晶中的应用

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This paper describes a method of dispensing a nanolitervolume of liquid into arrays of microwells through degassed poly(dimethylsiloxane) (PDMS) microchannels. In this method, the PDMS microchannels were reversibly bound to arrays of microwells. The PDMS elastomer was predegassed and served as an internal vacuum pumping source. Various aqueous solutions were infused into arrays of microwells through the reversibly sealed PDMS microchannels. Microwells fabricated in PDMS, poly(methyl methacrylate) (PMMA), and glass were all compatible with this dispensing method. By removing the PDMS microchannels, arrays of droplets confined in the microwells were obtained. Multiplex reaction and screening at the nanoliter scale were carried out by binding two such arrays of microwells to form microchambers. We applied this method to screening the crystallization conditions of four known proteins. Long-term incubation of over 2 months was achieved by employing glass microwells. An unknown protein was then crystallized using the screening method in microwells. The crystals with sufficient size were harvested from the reversibly bound microwells. X-ray diffraction with a resolution of 3.1 A was obtained.
机译:本文介绍了一种通过脱气的聚二甲基硅氧烷(PDMS)微通道将纳升体积的液体分配到微孔阵列中的方法。在这种方法中,PDMS微通道可逆地绑定到微孔阵列。 PDMS弹性体已预脱气并用作内部真空泵送源。通过可逆密封的PDMS微通道将各种水溶液注入微孔阵列中。用PDMS,聚甲基丙烯酸甲酯(PMMA)和玻璃制成的微孔都与这种分配方法兼容。通过去除PDMS微通道,获得了限制在微孔中的液滴阵列。通过结合两个这样的微孔阵列以形成微腔室,进行纳升级的多重反应和筛选。我们将这种方法应用于筛选四种已知蛋白质的结晶条件。通过使用玻璃微孔可实现2个月以上的长期孵育。然后使用微孔中的筛选方法将未知蛋白质结晶。从可逆结合的微孔中收获具有足够大小的晶体。获得分辨率为3.1 A的X射线衍射。

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