Literature DB >> 18166674

ABRF ESRG 2006 study: Edman sequencing as a method for polypeptide quantitation.

D C Brune1, B Hampton, R Kobayashi, J W Leone, K D Linse, J Pohl, R S Thoma, N D Denslow.   

Abstract

The Edman Sequencing Research Group (ESRG) designs studies on the use of Edman degradation for protein and peptide analysis. These studies provide a means for participating laboratories to compare their analyses against a benchmark of those from other laboratories that provide this valuable service. The main purpose of the 2006 study was to determine how accurate Edman sequencing is for quantitative analysis of polypeptides. Secondarily, participants were asked to identify a modified amino acid residue, N-epsilon-acetyl lysine [Lys(Ac)], present within one of the peptides. The ESRG 2006 peptide mixture consisted of three synthetic peptides. The Peptide Standards Research Group (PSRG) provided two peptides, with the following sequences: KAQYARSVLLEKDAEPDILELATGYR (peptide B), and RQAKVLLYSGR (peptide C). The third peptide, peptide C*, synthesized and characterized by ESRG, was identical to peptide C but with acetyl lysine in position 4. The mixture consisted of 20% peptide B and 40% each of peptide C and its acetylated form, peptide C*. Participating laboratories were provided with two tubes, each containing 100 picomoles of the peptide mixture (as determined by quantitative amino acid analysis) and were asked to provide amino acid assignments, peak areas, retention times at each cycle, as well as initial and repetitive yield estimates for each peptide in the mixture. Details about instruments and parameters used in the analysis were also collected. Participants in the study with access to a mass spectrometer (MALDI-TOF or ESI) were asked to provide information about the relative peak areas of the peptides in the mixture as a comparison with the peptide quantitation results from Edman sequencing. Positive amino acid assignments were 88% correct for peptide C and 93% correct for peptide B. The absolute initial sequencing yields were an average of 67% for peptide (C+C*) and 65.6 % for peptide B. The relative molar ratios determined by Edman sequencing were an average of 4.27 (expected ratio of 4) for peptides (C+C*)/B, and 1.49 for peptide C*/C (expected ratio of 1); the seemingly high 49% error in quantification of Lys(Ac) in peptide C* can be attributed to commercial unavailability of its PTH standard. These values compare very favorably with the values obtained by mass spectrometry.

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Year:  2007        PMID: 18166674      PMCID: PMC2392991     

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  5 in total

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Authors:  Scott D Buckel; Richard G Cook; J Myron Crawford; Nancy Denslow; Joseph Fernandez; Ben J Madden; John M Neveu
Journal:  J Biomol Tech       Date:  2003-12

2.  ABRF-98SEQ: Evaluation of peptide sequencing at high sensitivity.

Authors:  W J Henzel; A Admon; S A Carr; G Davis; K De Jongh; W Lane; M Rohde; L Steinke
Journal:  J Biomol Tech       Date:  2000-06

3.  Quantitative procedures for use with the Edman-Begg sequenator. Partial sequences of two unusual immunoglobulin light chains, Rzf and Sac.

Authors:  O Smithies; D Gibson; E M Fanning; R M Goodfliesh; J G Gilman; D L Ballantyne
Journal:  Biochemistry       Date:  1971-12-21       Impact factor: 3.162

4.  ABRF ESRG 2005 study: identification of seven modified amino acids by Edman sequencing.

Authors:  D Brune; N D Denslow; R Kobayashi; W S Lane; J W Leone; B J Madden; J M Neveu; J Pohl
Journal:  J Biomol Tech       Date:  2006-12

5.  ABRF-2002ESRG, a difficult sequence: Analysis of a PVDF-bound known protein with a heterogeneous amino-terminus.

Authors:  Scott D Buckel; Richard G Cook; J Myron Crawford; David R Dupont; Ben J Madden; John M Neveu; Laurey Steinke; Joseph Fernandez
Journal:  J Biomol Tech       Date:  2002-12
  5 in total
  5 in total

1.  A robust protocol to map binding sites of the 14-3-3 interactome: Cdc25C requires phosphorylation of both S216 and S263 to bind 14-3-3.

Authors:  Perry M Chan; Yuen-Wai Ng; Ed Manser
Journal:  Mol Cell Proteomics       Date:  2010-12-28       Impact factor: 5.911

2.  Crystallization and diffraction analysis of β-N-acetylhexosaminidase from Aspergillus oryzae.

Authors:  Ondřej Vaněk; Jiří Brynda; Kateřina Hofbauerová; Zdeněk Kukačka; Petr Pachl; Karel Bezouška; Pavlína Rezáčová
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2011-03-26

Review 3.  A Review of the Scientific Rigor, Reproducibility, and Transparency Studies Conducted by the ABRF Research Groups.

Authors:  Sheenah M Mische; Nancy C Fisher; Susan M Meyn; Katia Sol-Church; Rebecca L Hegstad-Davies; Frances Weis-Garcia; Marie Adams; John M Ashton; Kym M Delventhal; Julie A Dragon; Laura Holmes; Pratik Jagtap; Kristopher E Kubow; Christopher E Mason; Magnus Palmblad; Brian C Searle; Christoph W Turck; Kevin L Knudtson
Journal:  J Biomol Tech       Date:  2020-04

4.  Quantification of HLA class I molecules on renal cell carcinoma using Edman degradation.

Authors:  Juliane S Stickel; Natalie Stickel; Jörg Hennenlotter; Karin Klingel; Arnulf Stenzl; Hans-Georg Rammensee; Stefan Stevanović
Journal:  BMC Urol       Date:  2011-01-20       Impact factor: 2.264

5.  The ABRF Edman Sequencing Research Group 2008 Study: investigation into homopolymeric amino acid N-terminal sequence tags and their effects on automated Edman degradation.

Authors:  R S Thoma; J S Smith; W Sandoval; J W Leone; P Hunziker; B Hampton; K D Linse; N D Denslow
Journal:  J Biomol Tech       Date:  2009-09
  5 in total

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