Literature DB >> 19499054

Strategies for the synthesis of labeled peptides.

L Bibbs1, N P Ambulos, S A Kates, A Khatri, K F Medzihradszky, G Osapay, S T Weintraub.   

Abstract

Labeled peptides synthesized by core facilities are frequently used by researchers for following trafficking of a peptide, for binding studies, to determine substrate specificity, and for receptor cross-linking studies.The membership of the Association of Biomolecular Resource Facilities was asked to participate in a study focusing on synthesis of a biotin-labeled peptide, and it was suggested that a new strategy, using Rink amide 4-methylbenzhydrylamine resin coupled with Fmoc-Lys(Dde)-OH, be used.This strategy can be used for addition of a variety of labels other than biotin and should prove useful to core facilities. Comparison of the new strategy to other strategies was performed. Biotin labeling has long been assumed to be routine and specific. Despite the assumed routine nature of synthesizing biotinylated peptides, 9 of the 34 samples submitted did not contain any of the correct product. Although synthesis using Fmoc-Lys(Dde)-OH plus biotin generally gave the highest yields, other approaches also yielded a high percentage of the correct product.Therefore, the various strategies are generally comparable. The major advantage of this new approach is that other labels such as fluorescein, dansyl groups, methyl coumarin, and potentially fluorophores and quenchers used for fluorescence resonance energy transfer (FRET) can be directly incorporated into peptides.

Entities:  

Year:  2000        PMID: 19499054      PMCID: PMC2291636     

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


  7 in total

1.  Function-based isolation of novel enzymes from a large library.

Authors:  M J Olsen; D Stephens; D Griffiths; P Daugherty; G Georgiou; B L Iverson
Journal:  Nat Biotechnol       Date:  2000-10       Impact factor: 54.908

Review 2.  Six-year study of peptide synthesis.

Authors:  R H Angeletti; L F Bonewald; G B Fields
Journal:  Methods Enzymol       Date:  1997       Impact factor: 1.600

Review 3.  Solid-phase synthesis of cyclic homodetic peptides.

Authors:  C Blackburn; S A Kates
Journal:  Methods Enzymol       Date:  1997       Impact factor: 1.600

4.  Allyl-based groups for side-chain protection of amino-acids.

Authors:  A Loffet; H X Zhang
Journal:  Int J Pept Protein Res       Date:  1993-10

5.  Automated allyl cleavage for continuous-flow synthesis of cyclic and branched peptides.

Authors:  S A Kates; S B Daniels; F Albericio
Journal:  Anal Biochem       Date:  1993-08-01       Impact factor: 3.365

6.  A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis.

Authors:  D S King; C G Fields; G B Fields
Journal:  Int J Pept Protein Res       Date:  1990-09

7.  Preparation of the very acid-sensitive Fmoc-Lys(Mtt)-OH. Application in the synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the solid-phase assembly of MAPs and TASPs.

Authors:  A Aletras; K Barlos; D Gatos; S Koutsogianni; P Mamos
Journal:  Int J Pept Protein Res       Date:  1995-05
  7 in total
  1 in total

Review 1.  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
  1 in total

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