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Novel thermal phase transition behavior of phosphatidylcholine analogs containing 1,2,4-butanetriol as their backbone.

DIR@IMTECH: CSIR-Institute of Microbial Technology

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Title Novel thermal phase transition behavior of phosphatidylcholine analogs containing 1,2,4-butanetriol as their backbone.
 
Creator Arora, A
Gupta, C M
 
Subject QD Chemistry
 
Description The sn-glycerol moiety in 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) was replaced by the rac-1,2,4-butanetriol residue, and the aqueous dispersions of the resulting DPPC analogs, viz. 1,2-dihexadecanoyloxy-rac-but-4-yl-[2-(trimethyl-ammonium)ethyl]ph osphate (1,2-bPC) and 1,3-dihexadecanoyloxy-rac-but-4-yl-[2-(trimethylammonium)ethyl]pho sphate (1,3-bPC), were characterized by differential scanning calorimetry (DSC) and fluorescence polarization technique. Also, the corresponding (3R)-isomer of 1,3-bPC (1,3-(3R)bPC) was prepared and characterized by DSC. While the thermal phase transition properties of 1.2-bPC were similar to that of racemic DPPC, 1.3-bPC in identical conditions showed an abnormal property by exhibiting a metastable phase behavior at about 15 degrees C. This abnormal property was associated only with the racemic mixture and was completely absent in its 3R-isomer. 1,3-(3R)bPC, unlike DPPC, showed only two high enthalpy transitions at about 29.7 degrees C (delta H, 7.45 kcal/mol) and 35.3 degrees C (delta H, 6.93 kcal/mol). These results clearly demonstrate that an insertion of one additional methylene residue between the glycerol C1 and C2 carbons in DPPC markedly alters its thermal phase transitional properties, whereas these properties remain virtually unchanged if a similar chemical change is introduced between the glycerol C2 and C3 carbon atoms.
 
Publisher Elsevier Science
 
Date 1997-02-21
 
Type Article
PeerReviewed
 
Relation http://www.sciencedirect.com/science/article/pii/S0005273696002088
http://crdd.osdd.net/open/371/
 
Identifier Arora, A and Gupta, C M (1997) Novel thermal phase transition behavior of phosphatidylcholine analogs containing 1,2,4-butanetriol as their backbone. Biochimica et biophysica acta, 1324 (1). pp. 61-8. ISSN 0006-3002