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使用“芯片上的斑点”技术通过基质辅助激光解吸电离飞行时间质谱法鉴定蛋白质的信号放大。

Signal amplification using "spot-on-a-chip" technology for the identification of proteins via MALDI-TOF MS.

作者信息

Ekström S, Ericsson D, Onnerfjord P, Bengtsson M, Nilsson J, Marko-Varga G, Laurell T

机构信息

Department of Electrical Measurements, Lund University, Sweden.

出版信息

Anal Chem. 2001 Jan 15;73(2):214-9. doi: 10.1021/ac000734u.

Abstract

The presented "spot-on-a-chip" technology enables easy enrichment of samples in the low nanomolar (1-5 nM) range and provides a fast and reliable automated sample preparation method for performing matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis with high sensitivity and throughput. Through microdispensing, which allows accurate deposition of 60-pL droplets, dilute samples were enriched by making multiple droplet depositions in nanovials. The sample was confined to a defined spot area (300 x 300 microm), and multiple depositions increase the surface density of analyte in the nanovial, thereby providing detection of low attomole levels. The impact of the nanovial geometry with respect to the MALDI-TOF MS resolution for peptides deposited in the microfabricated silicon vials was investigated and the optimal geometry and size were determined. The spot-on-a-chip technology, that is, the combination of microdispensing, micromachined silicon nanovials and on-spot enrichment provides a signal amplification of at least 10-50 times as compared to an ordinary sample preparation. The linearity of the enrichment effect is shown by the analysis of a peptide mixture at the 5 nM level. The signal amplification provided by the spot-on-a-chip enrichment is demonstrated by the analysis of relevant biological samples, interleukin-8 from a spiked cell supernatant, and by successful protein identification of an excised spot from a high-sensitivity silver-stained two-dimensional electrophoresis gel separation.

摘要

所展示的“芯片上的点”技术能够轻松富集低纳摩尔(1 - 5 nM)范围内的样品,并提供一种快速且可靠的自动化样品制备方法,用于进行具有高灵敏度和高通量的基质辅助激光解吸/电离飞行时间质谱(MALDI - TOF MS)分析。通过微量分配,可精确沉积60皮升液滴,通过在纳米小瓶中进行多次液滴沉积来富集稀释样品。样品被限制在一个确定的斑点区域(300×300微米),多次沉积增加了纳米小瓶中分析物的表面密度,从而能够检测低阿托摩尔水平。研究了纳米小瓶几何形状对微加工硅制小瓶中沉积肽的MALDI - TOF MS分辨率的影响,并确定了最佳几何形状和尺寸。“芯片上的点”技术,即微量分配、微加工硅纳米小瓶和原位富集的结合,与普通样品制备相比,提供了至少10 - 50倍的信号放大。通过分析5 nM水平的肽混合物展示了富集效果的线性。通过分析相关生物样品(加标的细胞上清液中的白细胞介素 - 8)以及成功鉴定高灵敏度银染二维电泳凝胶分离中切下的斑点中的蛋白质,证明了“芯片上的点”富集提供的信号放大。

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