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1 ength and was dependent on the charge of the polar headgroup.
2 ttings into an average orientation of the PC polar headgroup.
3 dependent on the nature of the phospholipid polar headgroup.
4 izable nitroxide tag attached to the lipids' polar headgroup.
5 ctions between charged amino acids and lipid polar headgroups.
6 s as its electrostatic interactions with the polar headgroups.
7 cificity toward phospholipids with different polar headgroups.
8 oduct ions arising from the combined loss of polar headgroup and HNO2, [NO2-FA + H](+) and [NO2-FA -
9 omplex network of hydrogen bonds between the polar headgroup and the protein, while the 3-phenoxyphen
11 ues of RB-005, in which the lipophilic tail, polar headgroup, and linker region were modified to exte
12 routes enable the incorporation of different polar headgroups as well as nonpolar tails at late stage
13 ty also decreased the mobility of oleic acid polar headgroups, as well as the area/molecule of lipid.
14 low 60 muM preferentially interacts with the polar headgroups at the membrane-electrolyte interface,
15 mplexes have defined both the orientation of polar headgroups between the alpha1 and alpha2 helices o
16 y the lipid acyl length (bilayer thickness), polar headgroups (bilayer interfacial area), inclusion o
17 high-precision biological investigations of polar headgroup/biological target interactions of these
18 reveal (i) different thermal regulations and polar headgroup compositions of membrane lipids between
19 g the nitroxide moiety directly to the lipid polar headgroup defines the location of the measured pot
20 uctural changes involved either altering the polar headgroup (e.g., 6-ketocholestanol) or eliminating
21 by double acyl chains and by the presence of polar headgroups facilitating the entrance/exit of proto
24 shifts indicate that the conformation of the polar headgroup in these bicelles may be different from
28 ith a nitrophenylazido group attached to the polar headgroup of cardiolipin (CL) via a linker contain
31 sured for dansyl groups: (1) attached to the polar headgroup of PE, (2) linked to an alkyl chain, (3)
34 d exhibits unfavorable interactions with the polar headgroups of DPPC, thereby inducing a dehydration
38 es 2 and 3 appear to be interacting with the polar headgroups of the phospholipids or constitute a di
40 heir abundances do not depend on the type of polar headgroup or the number of double bonds of unsatur
41 lipid/sHsp interactions are mediated by the polar headgroup region and that the proteins strongly af
42 se hydrophilic peptides do not penetrate the polar headgroup region of the membrane and that the bind
43 cated that the V338C site was located in the polar headgroup region of the membrane, approximately 1.
44 d state, the drug was found to locate in the polar headgroup region of the phospholipid bilayer, to i
45 that the Laurdan chromophore resides in the polar headgroup region of the PLFE liposomes, while the
46 ~ 2) and suggest a large contribution of the polar headgroup region to the dielectric response of the
47 all cases, the dansyl probes located in the polar headgroup region, 19-21 A from the bilayer center.
49 icant decrease in water content in the lipid polar headgroup regions occurred during the first 1-2-h
50 of amphiphilic surfactants anchored by their polar headgroups; sliding occurs at the interface betwee
51 bility of ordered domains decreased with the polar headgroup structure of PO lipids in the order PE >
52 everal amphiphile molecules bind along their polar headgroup to the interface binding region (i-face)
53 show that bilayers containing steroids with polar headgroups undergo lateral phase separation, with
54 at cholesterol and ceramides both have small polar headgroups, we propose that ceramides and choleste
55 e grafted to the aqueous interface via their polar headgroups, whereas the fatty acyl chains are in e
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