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

被引:76
作者
Ekström, S
Ericsson, D
Önnerfjord, P
Bengtsson, M
Nilsson, J
Marko-Varga, G
Laurell, T
机构
[1] Univ Lund, Dept Elect Measurements, S-22100 Lund, Sweden
[2] Univ Lund, Dept Analyt Chem, S-22100 Lund, Sweden
[3] AstraZeneca, Mol Sci, R&D Lund, S-22187 Lund, Sweden
关键词
D O I
10.1021/ac000734u
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 mum), 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.
引用
收藏
页码:214 / 219
页数:6
相关论文
共 26 条
  • [1] Allmaier G, 1997, RAPID COMMUN MASS SP, V11, P1567, DOI 10.1002/(SICI)1097-0231(199709)11:14<1567::AID-RCM32>3.0.CO
  • [2] 2-0
  • [3] ANNAN RS, 1996, P 44 ASMS C MASS SPE, P702
  • [4] POLYETHYLENE MEMBRANE AS A SAMPLE SUPPORT FOR DIRECT MATRIX-ASSISTED LASER-DESORPTION IONIZATION MASS-SPECTROMETRIC ANALYSIS OF HIGH-MASS PROTEINS
    BLACKLEDGE, JA
    ALEXANDER, AJ
    [J]. ANALYTICAL CHEMISTRY, 1995, 67 (05) : 843 - 848
  • [5] Integrated microanalytical technology enabling rapid and automated protein identification
    Ekström, S
    Önnerfjord, P
    Nilsson, J
    Bengtsson, M
    Laurell, T
    Marko-Varga, G
    [J]. ANALYTICAL CHEMISTRY, 2000, 72 (02) : 286 - 293
  • [6] Gobom J, 1999, J MASS SPECTROM, V34, P105, DOI 10.1002/(SICI)1096-9888(199902)34:2<105::AID-JMS768>3.0.CO
  • [7] 2-4
  • [8] HEZEL WJ, 1993, P NATL ACAD SCI USA, V90, P5011
  • [9] Identification of the components of simple protein mixtures by high accuracy peptide mass mapping and database searching
    Jensen, ON
    Podtelejnikov, AV
    Mann, M
    [J]. ANALYTICAL CHEMISTRY, 1997, 69 (23) : 4741 - 4750
  • [10] ATTOMOLE DETECTION OF PROTEINS BY MATRIX-ASSISTED LASER-DESORPTION IONIZATION MASS-SPECTROMETRY WITH THE USE OF PICOLITRE VIALS
    JESPERSEN, S
    NIESSEN, WMA
    TJADEN, UR
    VANDERGREEF, J
    LITBORN, E
    LINDBERG, U
    ROERAADE, J
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1994, 8 (08) : 581 - 584