Hydrogen bond among the ionic groups of ampholytic phospholipid
β Scribed by T. Seimiya; M. Ashida; M. Hayashi; T. Muramatsu; I. Hara
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 665 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0009-3084
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β¦ Synopsis
The nature of interaction among t.he i6nic g~oups of lipids was studied by proton NMR meamrements for ampholytic analogues of phosphoh'pids, each dHf~ring in s~ctural separadon between PO?~ and NI~ groups, Single resonance ~s observ~ for the ionic p~otons of lJpids in deuterochloroform indicate the rapid exchange of protons between POoH and NH~, and showed that the two groups interact intramolecularly and/or intermo|ecule~ly by forming a hydrogea bond.
The hydrogen bond is found to be weak for dipalmitoylphosphafidyl-p~Β’,panolamine and -butanolamine but strong for bath the -ethanolamine and -pentanotamme. q~he hydrogen b<md counteracts with calcium bint~ing and is almost broken for calcium complexes of the li~ id,~.
π SIMILAR VOLUMES
The effect of a number of long chain compounds on the phase transition temperature, Tm. of several phospholipids was measured at different pH values by differential scanning calorinretry. Only single chain compounds capable of intermolecular hydrogen bonding interactions, such as pahnitic acid, hexa
## Abstract Molecularβorbital calculations are used to compare the hydrogenβbonding characteristics of the two carbonyl groups of uridine nucleosides. Various numbers of water molecules are allowed to interact with uracil. The hydrogenβbond energies and the effects of these bonds on the electronic