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PMID: 7461911 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human beta-endorphin: synthesis and characterization of analogs iodinated and tritiated at tyrosine residues 1 and 27.

International journal of peptide and protein research ·Vol. 16 ·No. 4 ·1980-10-00 ·Pages 311-20

Houghten RA, Chang WC, Li CH

Abstract

Three tritiated analogs of human beta-endorphin have been prepared from their corresponding iodinated analogs. The iodinated analogs (diiodotyrosine at positions 1, 27 or 1 and 27) were synthesized by the solid-phase method and were found to have biological and physical properties which were altered when compared with the native molecule. Catalytic exchange of these iodinated analogs in the presence of tritium yielded tritiated human beta-endorphins having full biological activity and specific activity of 50-100 Ci/mmol. Both the iodinated and tritiated beta-endorphin analogs were shown to be homogeneous by chromatography on carboxymethylcellulose, partition chromatography, paper chromatography, amino acid analysis, electrophoresis, high performance liquid chromatography, and isoelectric focusing on polyacrylamide.

MeSH Terms
Amino Acid Sequence Endorphins/chemical synthesis Humans Indicators and Reagents Iodides Methods Structure-Activity Relationship Tritium Tyrosine
Chemicals
Endorphins Indicators and Reagents Iodides Tritium Tyrosine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Houghten R A
Chang W C
Li C H
Article Info
Journal
International journal of peptide and protein research
Abbr.
Int J Pept Protein Res
ISSN
0367-8377
Published
1980-10-00
Pages
311-20
Language
English
Region
Denmark
NLM ID
0330420
Subset
IM
Grants
NIGMS NIH HHS · GM-2907 · United States
NIMH NIH HHS · MH-30245 · United States
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