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Circular Dichroism Study of Membrane Dynamics. Effects of Carboxymethy 1-Chitin

The circular dichroim (CD) active phospholipid bis(4‘- n-octanoxyazobenzene-4-carboxyl)-L-a-phosphatidylcholine (CDPC) was used to study the effects of carboxymethyl-chitin (CM-chitin) on the membrane dynamics. For this purpose, CD and electronic spectra were observed for a mixture of CM-chitin and...

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Bibliographic Details
Published in:Journal of biochemistry (Tokyo) 1990-02, Vol.107 (2), p.217-221
Main Authors: Nishiya, Takako, Ahmed, Sharmin
Format: Article
Language:English
Online Access:Get full text
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Summary:The circular dichroim (CD) active phospholipid bis(4‘- n-octanoxyazobenzene-4-carboxyl)-L-a-phosphatidylcholine (CDPC) was used to study the effects of carboxymethyl-chitin (CM-chitin) on the membrane dynamics. For this purpose, CD and electronic spectra were observed for a mixture of CM-chitin and liposomes composed of CDPC and egg lecithin (EPC) (50% CDPC-EPC-liposomes), and for a mixture of CM-chitin, 50% CDPC-EPC-liposomes, and EPC-liposomes. CM-chitin at concentrations higher than ca. 10− 5]M induced the increase of absorbance at 600 nm synchronized with the dilution of CDPC in 50% CDPC-EPC-liposomes by EPC matrix, indicating that CM-chitin induces the fusion among a few liposomes and/ or the lipid transfer through the transient liposome fusion. Temperature dependent CD spectra of a mixture of the 50% CDCP-EPC-liposomes and CM-chitin suggested that even high concentration of CM-chitin has no significant perturbation of the lipid organization in the membranes. The effects of CM-chitin on the leakage of [3H] sucrose from the EPC-liposomes were also studied. By the presence of 5× lO− 6M CM-chitin, the half-life for leakage of [3H] sucrose in plasma was increased by 4 times. This effect of CM-chitin was reduced by chitinase, while no effect was observed with lysozyme, suggesting that CM-chitin molecules are adsorbed on the liposome surface and stabilize the liposomes against the plasma proteins.
ISSN:0021-924X
DOI:10.1093/oxfordjournals.jbchem.a123029