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note
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The in meso crystallogenesis reported on herein makes use of MAGs containing cis monounsaturated fatty acids. A shorthand system for describing the chemical constitution of these lipids is referred to as the N.T MAG notation. (52) This is based on a simplistic view of the MAG molecule as an object consisting of a head, a neck, and a tail with the latter two joined by a trunk. Here the head of the MAG is the glycerol headgroup. It is in an ester linkage to the neck corresponding to that part of the acyl chain extending from its carboxyl carbon to the first carbon of the olefin. The trunk is the cis double bond. The tail extends from the second carbon of the olefin to the chains methyl terminus. In the N.T MAG notation, N and T correspond to the number of carbon atoms in the neck and tail, respectively. The total number of carbon atoms in the chain is the sum of N and T. Thus, 11.7 MAG represents monovaccenin, a MAG with a fatty acyl chain 18 carbon atoms long where the cis double bond resides between carbon atoms 11 and 12. It is an olefinic isomer of 9.9 MAG commonly known as monoolein.
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In a separate study using circular dichroism, we obtained evidence that gramicidin exists in the HHSH form when reconstituted into the bilayer of the cubic phase. (23) However, in that study a different reconstitution protocol was used which involved dissolving the peptide directly in the molten lipid. Thus, the peptide was not exposed to solvent as was the case in the current study. As noted, exposure to solvent may have an effect on the conformation adopted by gramicidin, and so a direct comparison between the two studies is not appropriate.
-
In a separate study using circular dichroism, we obtained evidence that gramicidin exists in the HHSH form when reconstituted into the bilayer of the cubic phase. (23) However, in that study a different reconstitution protocol was used which involved dissolving the peptide directly in the molten lipid. Thus, the peptide was not exposed to solvent as was the case in the current study. As noted, exposure to solvent may have an effect on the conformation adopted by gramicidin, and so a direct comparison between the two studies is not appropriate.
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