Tibavinsky Ivan A, Kottke Peter A, Fedorov Andrei G
George W. Woodruff School of Mechanical Engineering and ‡Parker H. Petit Institute for Bioengineering & Biosciences, Georgia Institute of Technology , Atlanta, Georgia 30332, United States.
Anal Chem. 2015 Jan 6;87(1):351-6. doi: 10.1021/ac5040083. Epub 2014 Dec 11.
Salt removal is a prerequisite for electrospray ionization mass spectrometry (ESI-MS) analysis of biological samples. Rapid desalting and a low volume connection to an electrospray tip are required for time-resolved measurements. We have developed a microfabricated desalting device that meets both requirements, thus providing the foundational technology piece for transient ESI-MS measurements of complex biological liquid specimens. In the microfabricated device, the sample flows in a channel separated from a higher flow rate, salt-free counter solution by a monolithically integrated nanoporous alumina membrane, which can support pressure differences between the flow channels of over 600 kPa. Salt is removed by exploiting the large difference in diffusivities between salts and the typical ESI-MS target bioanalytes, e.g., peptides and proteins. We demonstrate the capability to remove 95% of salt from a sample solution in ∼1 s while retaining sufficiently high concentration of a relatively low molecular weight protein, cytochrome-c, for ESI-MS detection.
去除盐分是对生物样品进行电喷雾电离质谱(ESI-MS)分析的前提条件。对于时间分辨测量而言,需要快速脱盐并以小体积连接至电喷雾尖端。我们开发了一种微制造脱盐装置,该装置满足了这两个要求,从而为复杂生物液体样本的瞬态ESI-MS测量提供了基础技术部件。在该微制造装置中,样品在一个通道中流动,该通道通过整体集成的纳米多孔氧化铝膜与流速更高的无盐反溶液分隔开,该膜能够承受超过600 kPa的流道间压力差。通过利用盐与典型的ESI-MS目标生物分析物(例如肽和蛋白质)之间扩散率的巨大差异来去除盐分。我们展示了在约1秒内从样品溶液中去除95%盐分的能力,同时保留足够高浓度的相对低分子量蛋白质细胞色素c用于ESI-MS检测。