Literature DB >> 11217742

Alpha-cyano-4-hydroxycinnamic acid affinity sample preparation. A protocol for MALDI-MS peptide analysis in proteomics.

J Gobom1, M Schuerenberg, M Mueller, D Theiss, H Lehrach, E Nordhoff.   

Abstract

We present a new MALD1 sample preparation technique for peptide analysis using the matrix alpha-cyano-4-hydroxy-cinnamic acid (CHCA) and prestructured sample supports. The preparation integrates sample purification, based on the affinity of microcrystalline CHCA for peptides, thereby simplifying the analysis of crude peptide mixtures. Enzymatic digests can thus be prepared directly, without preceding purification. Prepared samples are homogeneous, facilitating automatic spectra acquisition. This method allows preparation of large numbers of samples with little effort and without the need for automation. These features make the described preparation suitable for cost-efficient high-throughput protein identification. Performance of the sample preparation is demonstrated with in situ proteolytic digests of human brain proteins separated by two-dimensional gel electrophoresis.

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Year:  2001        PMID: 11217742     DOI: 10.1021/ac001241s

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  43 in total

1.  MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging.

Authors:  Sascha Sauer; Hans Lehrach; Richard Reinhardt
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

2.  Trypsin catalyzed 16O-to-18O exchange for comparative proteomics: tandem mass spectrometry comparison using MALDI-TOF, ESI-QTOF, and ESI-ion trap mass spectrometers.

Authors:  Manfred Heller; Hassan Mattou; Christoph Menzel; Xudong Yao
Journal:  J Am Soc Mass Spectrom       Date:  2003-07       Impact factor: 3.109

3.  Combination of two matrices results in improved performance of MALDI MS for peptide mass mapping and protein analysis.

Authors:  Sabrina Laugesen; Peter Roepstorff
Journal:  J Am Soc Mass Spectrom       Date:  2003-09       Impact factor: 3.109

4.  Proteomic response of barley leaves to salinity.

Authors:  Abdolrahman Rasoulnia; Mohammad Reza Bihamta; Seyed Ali Peyghambari; Houshang Alizadeh; Afrasyab Rahnama
Journal:  Mol Biol Rep       Date:  2010-12-23       Impact factor: 2.316

5.  High heterogeneity within the ribosomal proteins of the Arabidopsis thaliana 80S ribosome.

Authors:  Patrick Giavalisco; Daniel Wilson; Thomas Kreitler; Hans Lehrach; Joachim Klose; Johan Gobom; Paola Fucini
Journal:  Plant Mol Biol       Date:  2005-03       Impact factor: 4.076

6.  Liquid matrix deposition on conductive hydrophobic surfaces for tuning and quantitation in UV-MALDI mass spectrometry.

Authors:  Magnus Palmblad; Rainer Cramer
Journal:  J Am Soc Mass Spectrom       Date:  2007-01-16       Impact factor: 3.109

7.  Matrix assisted ionization: new aromatic and nonaromatic matrix compounds producing multiply charged lipid, peptide, and protein ions in the positive and negative mode observed directly from surfaces.

Authors:  Jing Li; Ellen D Inutan; Beixi Wang; Christopher B Lietz; Daniel R Green; Cory D Manly; Alicia L Richards; Darrell D Marshall; Steven Lingenfelter; Yue Ren; Sarah Trimpin
Journal:  J Am Soc Mass Spectrom       Date:  2012-08-16       Impact factor: 3.109

8.  Fungal effector protein AVR2 targets diversifying defense-related cys proteases of tomato.

Authors:  Mohammed Shabab; Takayuki Shindo; Christian Gu; Farnusch Kaschani; Twinkal Pansuriya; Raju Chintha; Anne Harzen; Tom Colby; Sophien Kamoun; Renier A L van der Hoorn
Journal:  Plant Cell       Date:  2008-04-30       Impact factor: 11.277

9.  Evaluation of a novel, integrated approach using functionalized magnetic beads, bench-top MALDI-TOF-MS with prestructured sample supports, and pattern recognition software for profiling potential biomarkers in human plasma.

Authors:  Xinyi Zhang; Sau-Mei Leung; Claudia R Morris; Mark K Shigenaga
Journal:  J Biomol Tech       Date:  2004-09

10.  Identification of the cellular prohibitin 1/prohibitin 2 heterodimer as an interaction partner of the C-terminal cytoplasmic domain of the HIV-1 glycoprotein.

Authors:  Vanessa Emerson; Denise Holtkotte; Tanya Pfeiffer; I-Hsuan Wang; Martina Schnölzer; Tore Kempf; Valerie Bosch
Journal:  J Virol       Date:  2009-11-11       Impact factor: 5.103

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