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作为一种固定相的毛细管通道聚合物 (C-CP) 纤维,用于基质辅助激光/解吸电离质谱法的蛋白质溶液的样品净化。

Capillary-channeled polymer (C-CP) fibers as a stationary phase for sample clean-up of protein solutions for matrix-assisted laser/desorption ionization mass spectrometry.

机构信息

Department of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC 29633, USA.

出版信息

J Am Soc Mass Spectrom. 2012 Aug;23(8):1419-23. doi: 10.1007/s13361-012-0399-6. Epub 2012 Jun 1.

Abstract

Capillary-channeled polymer (C-CP) fibers are employed in a micropipette tip format to affect a stationary phase for the solid phase extraction (SPE) of proteins from buffer solutions prior to MALDI-MS analysis. Proteins readily adsorb to the polypropylene (PP) C-CP fibers while buffer species are easily washed off the tips using DI-H(2)O. Elution of the solutes is achieved with an aliquot of 50:50 ACN:H(2)O, which is compatible with the subsequent spotting on the MALDI target with the matrix solution. Lysozyme and cytochrome c are used as test species, with a primary buffer composition of 100 mM Tris-HCl. In this case, direct MALDI-MS produces no discernible protein signals. SPE on the C-CP fibers yields high fidelity mass spectra for 1 μL sample volumes. Limits of detection for cytochrome c in 100 mM Tris-HCl are on the order of 40 nM. Extraction of cytochrome c from buffer concentrations of up to 1 M Tris-HCl, provides signal recoveries that are suppressed by only ~50% versus neat protein solutions. Finally, extraction of 3.1 μM cytochrome c from a synthetic urine matrix exhibits excellent recovery.

摘要

毛细管通道聚合物 (C-CP) 纤维被应用于微吸管尖端的形式,以影响蛋白质在 MALDI-MS 分析之前从缓冲溶液中的固相萃取 (SPE) 的固定相。蛋白质很容易吸附到聚丙烯 (PP) C-CP 纤维上,而缓冲物种很容易使用 DI-H(2)O 从尖端冲洗掉。使用 50:50 ACN:H(2)O 的等分试样洗脱溶质,这与随后用基质溶液在 MALDI 靶上点样兼容。溶菌酶和细胞色素 c 被用作测试物种,其主要缓冲组成是 100 mM Tris-HCl。在这种情况下,直接 MALDI-MS 不会产生可辨别的蛋白质信号。在 C-CP 纤维上进行 SPE 可获得 1 μL 样品体积的高保真质谱。在 100 mM Tris-HCl 中细胞色素 c 的检测限约为 40 nM。从高达 1 M Tris-HCl 的缓冲浓度中提取细胞色素 c 可提供信号回收率,与纯蛋白质溶液相比仅抑制约 50%。最后,从合成尿液基质中提取 3.1 μM 细胞色素 c 表现出优异的回收率。

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