Literature DB >> 11467542

Two-layer sample preparation method for MALDI mass spectrometric analysis of protein and peptide samples containing sodium dodecyl sulfate.

N Zhang1, A Doucette, L Li.   

Abstract

Sodium dodecyl sulfate (SDS) is widely used in protein sample workup. However, many mass spectrometric methods cannot tolerate the presence of this strong surfactant in a protein sample. We present a practical and robust technique based on a two-layer matrix/sample deposition method for the analysis of protein and peptide samples containing SDS by matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS). The two-layer method involves the deposition of a mixture of sample and matrix on top of a thin layer of matrix crystals. It was found that for SDS-containing samples, the intensity of the MALDI signals can be affected by the conditions of sample preparation: on-probe washing, choice of matrix, deposition method, solvent system, and protein-to-SDS ratio. However, we found that, under appropriate conditions, the two-layer method gave reliable MALDI signals for samples with levels of SDS up to approximately 1%. The applications of this method are demonstrated for MALDI analysis of hydrophobic membrane proteins as well as bacterial extracts. We envision that this two-layer method capable of handling impure samples including those containing SDS will play an important role in protein molecular weight analysis as well as in proteome identification by MALDI-MS and MS/MS.

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Year:  2001        PMID: 11467542     DOI: 10.1021/ac001418i

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


  6 in total

1.  Sodium cation affinities of commonly used MALDI matrices determined by guided ion beam tandem mass spectrometry.

Authors:  S D M Chinthaka; M T Rodgers
Journal:  J Am Soc Mass Spectrom       Date:  2012-04       Impact factor: 3.109

2.  Interactions between sodium dodecyl sulfate micelles and peptides during matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) of proteolytic digests.

Authors:  Rama Tummala; Kari B Green-Church; Patrick A Limbach
Journal:  J Am Soc Mass Spectrom       Date:  2005-09       Impact factor: 3.109

Review 3.  The Escherichia coli proteome: past, present, and future prospects.

Authors:  Mee-Jung Han; Sang Yup Lee
Journal:  Microbiol Mol Biol Rev       Date:  2006-06       Impact factor: 11.056

4.  MALDI mass spectrometry analysis of high molecular weight proteins from whole bacterial cells: pretreatment of samples with surfactants.

Authors:  Mohammed A Meetani; Kent J Voorhees
Journal:  J Am Soc Mass Spectrom       Date:  2005-09       Impact factor: 3.109

5.  Three-layer matrix/sample preparation method for MALDI MS analysis of low nanomolar protein samples.

Authors:  Bernd O Keller; Liang Li
Journal:  J Am Soc Mass Spectrom       Date:  2006-04-03       Impact factor: 3.109

6.  Isolation, Amino Acid Sequences, and Plausible Functions of the Galacturonic Acid-Binding Egg Lectin of the Sea Hare Aplysia kurodai.

Authors:  Shoko Motohashi; Mitsuru Jimbo; Tomohiro Naito; Takefumi Suzuki; Ryuichi Sakai; Hisao Kamiya
Journal:  Mar Drugs       Date:  2017-06-02       Impact factor: 5.118

  6 in total

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