Teng Chien-Hsun, Ho Kun-Chan, Lin Ya-Shiuan, Chen Yu-Chie
Department of Applied Chemistry, National Chiao Tung University, Hsinchu 300, Taiwan.
Anal Chem. 2004 Aug 1;76(15):4337-42. doi: 10.1021/ac049963x.
MALDI mass spectrometry is used widely in various fields because it has the characteristics of speed, ease of use, high sensitivity, and wide detectable mass range, but suppression effects between analyte molecules and interference from the sample matrix frequently arise during MALDI analysis. The suppression effects can be avoided if target species are isolated from complicated matrix solutions in advance. Herein, we proposed a novel method for achieving such a goal. We describe a strategy that uses gold nanoparticles to capture charged species from a sample solution. Generally, ionic agents, such as anionic or cationic stabilizers, encapsulate gold nanoparticles to prevent their aggregation in solution. These charged stabilizers at the surface of the gold particles are capable of attracting oppositely charged species from a sample solution through electrostatic interactions. We have employed this concept to develop nanoparticle-based probes that selectively trap and concentrate target species in sample solutions. Additionally, to readily isolate them from solution after attracting their target species, we used gold nanoparticles that are adhered to the surface of magnetic particles through S-Au bonding. A magnet can then be employed to isolate the Au@magnetic particles from the solution. The species trapped by the isolated particles were then characterized by MALDI MS after a simple washing. We demonstrate that Au@magnetic particles having negatively charged surfaces are suitable probes for selectively trapping positively charged proteins from aqueous solutions. In addition, we have employed Au@magnetic particle-based probes successfully to concentrate low amounts of peptide residues from the tryptic digest products of cytochrome c (10(-7) M).
基质辅助激光解吸电离质谱(MALDI-MS)因其具有分析速度快、操作简便、灵敏度高以及可检测质量范围广等特点,在各个领域得到了广泛应用。然而,在MALDI分析过程中,常常会出现分析物分子之间的抑制效应以及来自样品基质的干扰。如果能提前将目标物质与复杂的基质溶液分离,就可以避免这种抑制效应。在此,我们提出了一种实现这一目标的新方法。我们描述了一种利用金纳米颗粒从样品溶液中捕获带电物质的策略。一般来说,离子型试剂,如阴离子或阳离子稳定剂,会包裹金纳米颗粒以防止其在溶液中聚集。金颗粒表面的这些带电稳定剂能够通过静电相互作用从样品溶液中吸引带相反电荷的物质。我们运用这一概念开发了基于纳米颗粒的探针,用于在样品溶液中选择性地捕获和浓缩目标物质。此外,为了在吸引目标物质后便于将它们从溶液中分离出来,我们使用了通过S-Au键合附着在磁性颗粒表面的金纳米颗粒。然后可以使用磁铁从溶液中分离出金@磁性颗粒。经过简单洗涤后,通过MALDI MS对被分离颗粒捕获的物质进行表征。我们证明,表面带负电荷的金@磁性颗粒是从水溶液中选择性捕获带正电荷蛋白质的合适探针。此外,我们还成功地使用了基于金@磁性颗粒的探针从细胞色素c的胰蛋白酶消化产物(10⁻⁷ M)中浓缩少量的肽残基。