Wilm M, Mann M
Protein & Peptide Group, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Anal Chem. 1996 Jan 1;68(1):1-8. doi: 10.1021/ac9509519.
The nanoelectrospray ion source (nanoES) has recently been developed and described theoretically. It is different from conventional electrospray sources and from other miniaturized electrospray sources by (i) its 1-2 microns spraying orifice achieved by pulling the spraying capillary to a fine tip, (ii) its very low flow rate of approximately 20 nL/min and the small size of droplets it generates, and (iii) the absence of solvent pumps and inlet valves. The fabrication and operation of nanoES needles is described in detail. Solutions with up to 0.1 M salt contents could be sprayed without sheath flow or pneumatic assist. Improved desolvation in nanoES led to instrument-limited resolution of the signals of a glycoprotein and the ability to signal average extensively allowed the C-terminal sequencing of a 40 kDa protein. Extensive mass spectrometric and tandem mass spectrometric investigation of the components of an unseparated peptide mixture was demonstrated by verification of 93% of the sequence of carbonic anhydrase. A rapid and robust desalting/concentration step coupled to the nanoES procedure allows the direct analysis of impure samples such as peptide mixtures extracted after in-gel digestion.
纳米电喷雾离子源(nanoES)最近已被开发并进行了理论描述。它与传统电喷雾源以及其他小型化电喷雾源的不同之处在于:(i)通过将喷雾毛细管拉成细尖端实现1-2微米的喷雾孔;(ii)其极低的流速约为20纳升/分钟以及所产生的小液滴尺寸;(iii)不存在溶剂泵和进样阀。详细描述了nanoES针的制作和操作。盐含量高达0.1M的溶液无需鞘流或气动辅助即可喷雾。nanoES中改进的去溶剂化导致糖蛋白信号的仪器极限分辨率,并且广泛的信号平均能力使得能够对40kDa的蛋白质进行C端测序。通过验证碳酸酐酶93%的序列,证明了对未分离肽混合物的成分进行广泛的质谱和串联质谱研究。与nanoES程序相结合的快速且强大的脱盐/浓缩步骤允许直接分析不纯样品,例如凝胶内消化后提取的肽混合物。