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PMID: 14684320 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Synthesis of hydrophilic and flexible linkers for peptide derivatization in solid phase.

Bioorganic & medicinal chemistry letters ·Vol. 14 ·No. 1 ·2004-01-05 ·Pages 161-5

Song A, Wang X, Zhang J, Marík J, Lebrilla CB, Lam KS

Abstract

Four N-Fmoc protected polyoxyethylene-based amino acid type linkers were designed and synthesized for peptide derivatization in solid phase. Three of them were obtained in a crystalline form. The crystallized linkers can be stored at 4 degrees C for 2 years without significant decomposition. Protocols for biotinylation and fluorescent labeling of peptides in solid phase were developed. The linkers also provide good ionization ability for single-bead mass spectrometry analysis of peptides.

MeSH Terms
Biotinylation Chromatography, High Pressure Liquid Combinatorial Chemistry Techniques Nuclear Magnetic Resonance, Biomolecular Peptides/chemical synthesis Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Chemicals
Peptides
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Song Aimin
Division of Hematology and Oncology, Department of Internal Medicine, UC Davis Cancer Center, University of California-Davis, 4501 X Street, Sacramento, CA 95817, USA.
Wang Xiaobing
Zhang Jinhua
Marík Jan
Lebrilla Carlito B
Lam Kit S
Article Info
Journal
Bioorganic & medicinal chemistry letters
Abbr.
Bioorg Med Chem Lett
ISSN
0960-894X
Published
2004-01-05
Pages
161-5
Language
English
Region
England
NLM ID
9107377
Subset
IM
Grants
NCI NIH HHS · R33 CA 86364 · United States
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