Literature DB >> 21731543

Novel Sample Preparation for Mass Spectral Analysis of Complex Biological Samples.

Eric A Porsch1, Cecelia A Shertz, Michael D Boyle.   

Abstract

The ability to combine a selective capture strategy with on chip MALDI-TOF analysis allows for rapid, sensitive analysis of a variety of different analytes. In this overview a series of applications of capture enhanced laser desorption ionization time of flight (CELDI-TOF) mass spectrometry are described. The key feature of the assay is an off-chip capture step that utilizes high affinity bacterial binding proteins to capture a selected ligand. This allows large volumes of sample to be used and provides for a concentration step prior to transfer to a gold chip for traditional mass spectral analysis. The approach can also be adapted to utilize specific antibody as the basis of the capture step. The direct and indirect CELDI-TOF assays are rapid, reproducible and can be a valuable proteomic tool for analysis of low abundance molecules present in complex mixtures like blood plasma.

Entities:  

Year:  2010        PMID: 21731543      PMCID: PMC3128501          DOI: 10.2174/157016410791330589

Source DB:  PubMed          Journal:  Curr Proteomics        ISSN: 1570-1646            Impact factor:   0.837


  60 in total

1.  The ProteinChip System from Ciphergen: a new technique for rapid, micro-scale protein biology.

Authors:  H A Davies
Journal:  J Mol Med (Berl)       Date:  2000       Impact factor: 4.599

2.  Streptococcal pyrogenic exotoxin B enhances tissue damage initiated by other Streptococcus pyogenes products.

Authors:  M Saouda; W Wu; P Conran; M D Boyle
Journal:  J Infect Dis       Date:  2001-08-10       Impact factor: 5.226

Review 3.  Nanotechnologies in proteomics.

Authors:  Yuri D Ivanov; Vadim M Govorun; Victor A Bykov; Alexander I Archakov
Journal:  Proteomics       Date:  2006-03       Impact factor: 3.984

Review 4.  Recent developments in the site-specific immobilization of proteins onto solid supports.

Authors:  Julio A Camarero
Journal:  Biopolymers       Date:  2008       Impact factor: 2.505

5.  A secreted streptococcal cysteine protease can cleave a surface-expressed M1 protein and alter the immunoglobulin binding properties.

Authors:  R Raeder; M Woischnik; A Podbielski; M D Boyle
Journal:  Res Microbiol       Date:  1998-09       Impact factor: 3.992

6.  Cloning and characterisation of a cysteine proteinase gene expressed in amastigotes of Leishmania (L.) amazonensis.

Authors:  Fernanda Lasakosvitsch; Luciana Girotto Gentil; Márcia Regina Machado dos Santos; José Franco da Silveira; Clara Lúcia Barbiéri
Journal:  Int J Parasitol       Date:  2003-04       Impact factor: 3.981

Review 7.  Renal tubule albumin transport.

Authors:  Michael Gekle
Journal:  Annu Rev Physiol       Date:  2005       Impact factor: 19.318

8.  Mapping of the human plasmin domain recognized by the unique plasmin receptor of group A streptococci.

Authors:  C C Broder; R Lottenberg; M D Boyle
Journal:  Infect Immun       Date:  1989-09       Impact factor: 3.441

9.  Association between expression of immunoglobulin G-binding proteins by group A streptococci and virulence in a mouse skin infection model.

Authors:  R Raeder; M D Boyle
Journal:  Infect Immun       Date:  1993-04       Impact factor: 3.441

10.  Application of immunoproteomics to analysis of post-translational processing of the antiphagocytic M protein of Streptococcus.

Authors:  Terence G Romer; Michael D P Boyle
Journal:  Proteomics       Date:  2003-01       Impact factor: 3.984

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