Literature DB >> 20722421

A quantitative study of the effects of chaotropic agents, surfactants, and solvents on the digestion efficiency of human plasma proteins by trypsin.

Jennifer L Proc1, Michael A Kuzyk, Darryl B Hardie, Juncong Yang, Derek S Smith, Angela M Jackson, Carol E Parker, Christoph H Borchers.   

Abstract

Plasma biomarkers studies are based on the differential expression of proteins between different treatment groups or between diseased and control populations. Most mass spectrometry-based methods of protein quantitation, however, are based on the detection and quantitation of peptides, not intact proteins. For peptide-based protein quantitation to be accurate, the digestion protocols used in proteomic analyses must be both efficient and reproducible. There have been very few studies, however, where plasma denaturation/digestion protocols have been compared using absolute quantitation methods. In this paper, 14 combinations of heat, solvent [acetonitrile, methanol, trifluoroethanol], chaotropic agents [guanidine hydrochloride, urea], and surfactants [sodium dodecyl sulfate (SDS) and sodium deoxycholate (DOC)] were compared with respect to their effectiveness in improving subsequent tryptic digestion. These digestion protocols were evaluated by quantitating the production of proteotypic tryptic peptides from 45 moderate- to high-abundance plasma proteins, using tandem mass spectrometry in multiple reaction monitoring mode, with a mixture of stable-isotope labeled analogues of these proteotypic peptides as internal standards. When the digestion efficiencies of these 14 methods were compared, we found that both of the surfactants (SDS and DOC) produced an increase in the overall yield of tryptic peptides from these 45 proteins, when compared to the more commonly used urea protocol. SDS, however, can be a serious interference for subsequent mass spectrometry. DOC, on the other hand, can be easily removed from the samples by acid precipitation. Examining the results of a reproducibility study, done with 5 replicate digestions, DOC and SDS with a 9 h digestion time produced the highest average digestion efficiencies (∼80%), with the highest average reproducibility (<5% error, defined as the relative deviation from the mean value). However, because of potential interferences resulting from the use of SDS, we recommend DOC with a 9 h digestion procedure as the optimum protocol.

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Year:  2010        PMID: 20722421      PMCID: PMC2996461          DOI: 10.1021/pr100656u

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  31 in total

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2.  Efficient and specific trypsin digestion of microgram to nanogram quantities of proteins in organic-aqueous solvent systems.

Authors:  Michael Brad Strader; David L Tabb; W Judson Hervey; Chongle Pan; Gregory B Hurst
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3.  A quantitative analysis of Arabidopsis plasma membrane using trypsin-catalyzed (18)O labeling.

Authors:  Clark J Nelson; Adrian D Hegeman; Amy C Harms; Michael R Sussman
Journal:  Mol Cell Proteomics       Date:  2006-04-24       Impact factor: 5.911

4.  Identification of membrane proteins from mammalian cell/tissue using methanol-facilitated solubilization and tryptic digestion coupled with 2D-LC-MS/MS.

Authors:  Josip Blonder; King C Chan; Haleem J Issaq; Timothy D Veenstra
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

5.  Multiple reaction monitoring-based, multiplexed, absolute quantitation of 45 proteins in human plasma.

Authors:  Michael A Kuzyk; Derek Smith; Juncong Yang; Tyra J Cross; Angela M Jackson; Darryl B Hardie; N Leigh Anderson; Christoph H Borchers
Journal:  Mol Cell Proteomics       Date:  2009-05-01       Impact factor: 5.911

6.  Molecular mechanism for the denaturation of proteins by urea.

Authors:  Jorge Almarza; Luis Rincon; Ali Bahsas; Francisco Brito
Journal:  Biochemistry       Date:  2009-08-18       Impact factor: 3.162

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9.  Evaluation of the application of sodium deoxycholate to proteomic analysis of rat hippocampal plasma membrane.

Authors:  Jian Zhou; Tieyang Zhou; Rui Cao; Zhen Liu; Jianying Shen; Ping Chen; Xianchun Wang; Songping Liang
Journal:  J Proteome Res       Date:  2006-10       Impact factor: 4.466

10.  Papaya glutamine cyclase, a plant enzyme highly resistant to proteolysis, adopts an all-beta conformation.

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  56 in total

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2.  Technology development: an overview.

Authors:  Christoph H Borchers
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3.  Quantitative assessment of in-solution digestion efficiency identifies optimal protocols for unbiased protein analysis.

Authors:  Ileana R León; Veit Schwämmle; Ole N Jensen; Richard R Sprenger
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Review 4.  Optimized approaches for quantification of drug transporters in tissues and cells by MRM proteomics.

Authors:  Bhagwat Prasad; Jashvant D Unadkat
Journal:  AAPS J       Date:  2014-04-22       Impact factor: 4.009

5.  Strategies of Drug Transporter Quantitation by LC-MS: Importance of Peptide Selection and Digestion Efficiency.

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Journal:  AAPS J       Date:  2017-06-06       Impact factor: 4.009

6.  Multiplexed quantitation of endogenous proteins in dried blood spots by multiple reaction monitoring-mass spectrometry.

Authors:  Andrew G Chambers; Andrew J Percy; Juncong Yang; Alexander G Camenzind; Christoph H Borchers
Journal:  Mol Cell Proteomics       Date:  2012-12-07       Impact factor: 5.911

7.  Absolute quantification of transcription factors during cellular differentiation using multiplexed targeted proteomics.

Authors:  Jovan Simicevic; Adrien W Schmid; Paola A Gilardoni; Benjamin Zoller; Sunil K Raghav; Irina Krier; Carine Gubelmann; Frédérique Lisacek; Felix Naef; Marc Moniatte; Bart Deplancke
Journal:  Nat Methods       Date:  2013-04-14       Impact factor: 28.547

8.  Targeted Proteomics for Multiplexed Verification of Markers of Colorectal Tumorigenesis.

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9.  Comprehensive analysis of protein digestion using six trypsins reveals the origin of trypsin as a significant source of variability in proteomics.

Authors:  Scott J Walmsley; Paul A Rudnick; Yuxue Liang; Qian Dong; Stephen E Stein; Alexey I Nesvizhskii
Journal:  J Proteome Res       Date:  2013-11-14       Impact factor: 4.466

10.  Quantitative Assessment of the Effects of Trypsin Digestion Methods on Affinity Purification-Mass Spectrometry-based Protein-Protein Interaction Analysis.

Authors:  Yueqing Zhang; Hong Sun; Jing Zhang; Allan R Brasier; Yingxin Zhao
Journal:  J Proteome Res       Date:  2017-07-20       Impact factor: 4.466

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