Literature DB >> 19499042

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

W J Henzel1, A Admon, S A Carr, G Davis, K De Jongh, W Lane, M Rohde, L Steinke.   

Abstract

The ABRF-98SEQ sample was the 11th in a series of amino acid sequencing studies performed by the Protein Sequence Research Group of the Association of Biomolecular Resource Facilities. This study was designed to aid participants' laboratories in determining their abilities to analyze the amino acid sequence of a peptide at high sensitivity using Edman degradation, mass spectrometry (MS), or both. ABRF-98SEQ is a 17-amino acid synthetic peptide (IFDDEIEEVQALYPTER) that resembles a typical tryptic peptide. It was distributed at the 2.8-pmol level. The sample was sent dried in a microfuge tube accompanied by instructions on solubilizing the sample and by a survey form. Including tentative calls, the correct sequence was obtained by 16% of the responding participants, compared with only 6% in the 1997 study when the low-level peptide was a minor component of a mixture. This increase probably reflects the purity of ABRF-98SEQ. A secondary factor in the increase in correct calls may be the larger number of respondents this year reporting that they perform sequence analysis at the 1- to 10-pmol level. Most respondents who obtained the correct sequence used a combination of Edman sequencing and molecular weight determination by MS. Overall, the accuracy and sensitivity of peptide sequencing by Edman degradation continue to improve and are clearly aided by the use of MS for molecular weight determination. Although peptide sequencing by MS is not yet routinely practiced by the participating laboratories, results of this study indicate that MS-derived sequence data, when properly interpreted, are valuable for correcting, completing, or corroborating sequence assignments derived by Edman.

Entities:  

Year:  2000        PMID: 19499042      PMCID: PMC2291621     

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


  8 in total

1.  De novo peptide sequencing via tandem mass spectrometry.

Authors:  V Dancík; T A Addona; K R Clauser; J E Vath; P A Pevzner
Journal:  J Comput Biol       Date:  1999 Fall-Winter       Impact factor: 1.479

2.  Using a matrix-assisted laser desorption/ionization time-of-flight mass spectrometer for combined in-source decay/post-source decay experiments.

Authors:  T Pfeifer; M Drewello; A Schierhorn
Journal:  J Mass Spectrom       Date:  1999-06       Impact factor: 1.982

3.  A method for high-sensitivity peptide sequencing using postsource decay matrix-assisted laser desorption ionization mass spectrometry.

Authors:  T Keough; R S Youngquist; M P Lacey
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

4.  A strategy for rapid and efficient sequencing of Lys-C peptides by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry post-source decay.

Authors:  T Pfeifer; P Rücknagel; G Kuellertz; A Schierhorn
Journal:  Rapid Commun Mass Spectrom       Date:  1999       Impact factor: 2.419

5.  Sequencing of peptides by tandem mass spectrometry and high-energy collision-induced dissociation.

Authors:  K Biemann
Journal:  Methods Enzymol       Date:  1990       Impact factor: 1.600

6.  Automated interpretation of high-energy collision-induced dissociation spectra of singly protonated peptides by 'SeqMS', a software aid for de novo sequencing by tandem mass spectrometry.

Authors:  J Fernandez-de-Cossio; J Gonzalez; L Betancourt; V Besada; G Padron; Y Shimonishi; T Takao
Journal:  Rapid Commun Mass Spectrom       Date:  1998       Impact factor: 2.419

7.  De novo peptide sequencing in an ion trap mass spectrometer with 18O labeling.

Authors:  J Qin; C J Herring; X Zhang
Journal:  Rapid Commun Mass Spectrom       Date:  1998       Impact factor: 2.419

8.  Sequence database searches via de novo peptide sequencing by tandem mass spectrometry.

Authors:  J A Taylor; R S Johnson
Journal:  Rapid Commun Mass Spectrom       Date:  1997       Impact factor: 2.419

  8 in total
  5 in total

1.  ABRF-ESRG'03: analysis of a PVDF-bound known protein with a homogeneous amino-terminus.

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

Review 2.  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

3.  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

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

Authors:  D C Brune; B Hampton; R Kobayashi; J W Leone; K D Linse; J Pohl; R S Thoma; N D Denslow
Journal:  J Biomol Tech       Date:  2007-12

5.  Antibacterial activities of two potential peptides extracted from Polistes wattii Cameron, 1900 (Vespidae: Polistinae) wasp venom collected at Eastern Province, Saudi Arabia.

Authors:  Kholoud A Al-Shammery; Wael N Hozzein
Journal:  PLoS One       Date:  2022-03-07       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.