Department of Chemistry and The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
ColumnScientific Inc., Xiamen 361102, China.
J Chromatogr A. 2021 Jul 5;1648:462218. doi: 10.1016/j.chroma.2021.462218. Epub 2021 May 1.
Due to its unique structure, core-shell material has presented significantly improved chromatographic performance in comparison with conventional totally porous material. This has been well demonstrated in the analytical column format, e.g. 4.6 mm i.d. columns. In the proteomics field, there is always a demand for high resolution microseparation tools. In order to explore core-shell material's potential in proteomics-oriented microseparations, we investigated chromatographic performance of core-shell material in a nanoLC format, as well as its resolving power for protein digests. The results show core-shell nanoLC columns have similar van Deemter curves to the totally porous particle-packed nanoLC columns. For 100 µm i.d. capillary columns, the core-shell material does not have significantly better dynamics. However, both core-shell and totally porous particle-packed nanoLC columns have shown high efficiencies: plate heights of ~11 µm, equivalent to 90000 plates per meter, have been achieved with 5 µm particles. Using a 60 cm long core-shell nanoLC column, 72000 plates were realized in an isocratic separation of neutral compounds. For a 15 cm long nanoLC column, a maximum peak capacity of 220 has been achieved in a 5 hour gradient separation of protein digests, indicating the high resolving power of core-shell nanoLC columns. With a standard HeLa cell lysate as the sample, 2546 proteins were identified by using the core-shell nanoLC column, while 2916 proteins were identified by using the totally porous particle-packed nanoLC column. Comparing the two sets of proteomics data, it was found that 1830 proteins were identified by both columns, while 1086 and 716 proteins were uniquely identified by using totally porous and core-shell particle-packed nanoLC columns, respectively, suggesting their complementarity in nanoLC-MS based proteomics.
由于其独特的结构,核壳材料在色谱性能方面与传统的全多孔材料相比有显著提高。这在分析柱形式中得到了很好的证明,例如 4.6mmID 柱。在蛋白质组学领域,人们总是需要高分辨率的微分离工具。为了探索核壳材料在面向蛋白质组学的微分离中的潜力,我们研究了核壳材料在纳升液相色谱(nanoLC)形式中的色谱性能,以及其对蛋白质消化物的分辨能力。结果表明,核壳纳升液相色谱柱与全多孔颗粒填充纳升液相色谱柱具有相似的范德姆特曲线。对于 100µmID 的毛细管柱,核壳材料并没有明显更好的动力学性能。然而,核壳和全多孔颗粒填充的纳升液相色谱柱都表现出了很高的效率:使用 5µm 颗粒,达到了约 11µm 的板高,相当于每米 90000 块板。使用 60cm 长的核壳纳升液相色谱柱,在中性化合物的等度分离中实现了 72000 块板。在 15cm 长的纳升液相色谱柱上,在蛋白质消化物的 5 小时梯度分离中实现了最大峰容量 220,表明核壳纳升液相色谱柱具有很高的分辨能力。以标准的 HeLa 细胞裂解液作为样品,使用核壳纳升液相色谱柱鉴定到 2546 种蛋白质,而使用全多孔颗粒填充纳升液相色谱柱鉴定到 2916 种蛋白质。比较这两组蛋白质组学数据发现,有 1830 种蛋白质被两种柱子共同鉴定到,而分别有 1086 种和 716 种蛋白质被全多孔和核壳颗粒填充的纳升液相色谱柱所特有鉴定到,这表明它们在基于纳升液相色谱-质谱的蛋白质组学中具有互补性。