Formation of cross-links and fluorescence in polylysine, soluble proteins and membrane proteins by reaction with 1-butanal.
- 1 January 1988
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 36 (2) , 685-692
- https://doi.org/10.1248/cpb.36.685
Abstract
The reaction of polylysine and 1-butanal afforded 2-ethyl-2-hexenal, an aldol condensation and dehydration product of 1-butanal. 1-Butanal and 2-ethyl-2-hexenal were able to form fluorescence in polylysine, bovine serum albumin and erythrocyte membrane proteins. They were able to cross-link polylysine, hemoglobin, erythrocyte membrane proteins and isolated spectrin. Formation of cross-links by these aldehydes depended on the kind of protein. The ability of the proteins to form cross-links may reflect the contents of functional groups responsible and the quaternary structures of the proteins. 1-Butanal and 2-ethyl-2-hexenal may participate in the formation of cross-links and fluorescence by interaction with amino groups in the proteins.This publication has 4 references indexed in Scilit:
- Formation of fluorescent substances in reaction of aliphatic aldehydes and methylamineJournal of Oil & Fat Industries, 1987
- Fluorescent and cross-linked proteins of human erythrocyte ghosts formed by reaction with hydroperoxylinoleic acid, malonaldehyde and monofunctional aldehydes.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Self-assembly of spectrin oligomers in vitro: a basis for a dynamic cytoskeleton.The Journal of cell biology, 1981
- Polymerization of membrane components in aging red blood cellsBiochemical and Biophysical Research Communications, 1980