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1 sterol, dipalmitoyl phosphatidylcholine, and dioleoylphosphatidylcholine.
2 lesterol, distearoylphosphatidylcholine, and dioleoylphosphatidylcholine.
3 s within model membrane vesicles composed of dioleoylphosphatidylcholine.
5 ynamic averaging in bilayer membranes of 1,2-dioleoylphosphatidylcholine, 1,2-dimyristoylphosphatidyl
7 vesicles in a limiting volume of water [D2O:dioleoylphosphatidylcholine:alamethicin; 220:1:0.05; (M:
8 ees C and 37 degrees C DSMs were enriched in dioleoylphosphatidylcholine and DRMs were enriched in SM
9 We show that bilayers composed of equimolar dioleoylphosphatidylcholine and sphingomyelin spontaneou
10 s (P-23, P-29) into bilayers composed of SM, dioleoylphosphatidylcholine, and cholesterol, separated
11 aft stability in vesicles containing sterol, dioleoylphosphatidylcholine, and one of the following or
13 nosecond molecular dynamics simulations of a dioleoylphosphatidylcholine bilayer at 66% RH (5.4 water
14 r determining the structure of a fluid-phase dioleoylphosphatidylcholine bilayer from x-ray and neutr
15 ynamics of the lipid and water components of dioleoylphosphatidylcholine bilayers at various levels o
17 from mixtures of various molar fractions of dioleoylphosphatidylcholine, cholesterol, and egg sphing
18 induced in such simple lipid compositions as dioleoylphosphatidylcholine/cholesterol (DOPC)/chol) whi
19 was found that when the T domain is added to dioleoylphosphatidylcholine-containing vesicles, all thr
20 ectrum of Dauda bound to KcsA in bilayers of dioleoylphosphatidylcholine contains three components, w
22 ift in the fluorescence emission spectrum in dioleoylphosphatidylcholine [di(C18:1)PC] but smaller sh
24 on of small unilamellar vesicles composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
25 PEG-mediated fusion of SUVs composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
26 25 nm small unilamellar vesicles composed of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
27 ilinoleoylphosphatidylcholine), a mixture of dioleoylphosphatidylcholine, dioleoylphosphatidylethanol
28 on of small unilamellar vesicles composed of dioleoylphosphatidylcholine/dioleoylphosphatidylethanola
30 were incorporated into vesicles composed of dioleoylphosphatidylcholine (DOPC) adopted a topography
31 lly labeled M2-TMPs were studied in hydrated dioleoylphosphatidylcholine (DOPC) and dimyristoylphosph
32 s was investigated using a mixture either of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
33 er, previous investigations on the system of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
34 ogenous cardiolipin added in the presence of dioleoylphosphatidylcholine (DOPC) and dioleoylphosphati
36 The importance of helper lipids, including dioleoylphosphatidylcholine (DOPC) and phosphatidylethan
37 he peptide in lipid compositions formed from dioleoylphosphatidylcholine (DOPC) and varied percentage
38 uid argon system, and then applied to a neat dioleoylphosphatidylcholine (DOPC) bilayer at 66% relati
39 ceramide (PCer) or other ceramide analogs in dioleoylphosphatidylcholine (DOPC) bilayers has been exa
41 ers with a biologically relevant width, i.e. dioleoylphosphatidylcholine (DOPC) bilayers), while poly
42 y the kinetics of folding and insertion into dioleoylphosphatidylcholine (DOPC) bilayers, as a functi
46 brain sphingomyelin (bSM) was exchanged into dioleoylphosphatidylcholine (DOPC) GUVs, lateral diffusi
47 y the oligomeric structure of PLB in SDS and dioleoylphosphatidylcholine (DOPC) lipid bilayers recons
50 l phosphatidylcholine (DPPC)), low-Tm lipid (dioleoylphosphatidylcholine (DOPC) or 1-palmitoyl 2-oleo
51 4 carbons, were incorporated separately into dioleoylphosphatidylcholine (DOPC) or dioleoylphosphatid
52 ared using binary mixtures of bis-SorbPC and dioleoylphosphatidylcholine (DOPC) revealed a similar NM
53 ifferent vesicle systems have been compared: dioleoylphosphatidylcholine (DOPC) small unilamellar ves
54 tely 6:4 POPC:cholesterol<POPC approximately dioleoylphosphatidylcholine (DOPC)<1,2-dioleoyl-sn-glyce
56 em consisting of NADPH-P450 reductase (CPR), dioleoylphosphatidylcholine (DOPC), an ionic detergent,
57 LPC), dimyristoylphosphatidylcholine (DMPC), dioleoylphosphatidylcholine (DOPC), and 1-palmitoyl-2-ol
58 phase dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine (DOPC), and cholesterol show
59 e lipids with different physical properties, dioleoylphosphatidylcholine (DOPC), dioleoylphosphatidyl
60 method was applied to a system consisting of dioleoylphosphatidylcholine (DOPC), egg sphingomyelin (e
61 tion of SP with bilayers, composed of either dioleoylphosphatidylcholine (DOPC), or a 50:50 mixture o
62 solid-supported lipid bilayers consisting of dioleoylphosphatidylcholine (DOPC), palmitoyloleoylphosp
63 predominant lipids in the outer leaflet and dioleoylphosphatidylcholine (DOPC), POPC, 1-palmitoyl-2-
64 dioleoylphosphatidylethanolamine (DOPE) and dioleoylphosphatidylcholine (DOPC), the proteins produce
65 osphatidylethanolamine (DOPE), together with dioleoylphosphatidylcholine (DOPC), to the photochemistr
71 gg yolk phosphatidylcholine (egg PC) or from dioleoylphosphatidylcholine (DOPC)/dilinolenoylphosphati
72 n, we studied the lipid mixing kinetics with dioleoylphosphatidylcholine (DOPC)/ganglioside GD1a (GD1
73 defined tilted transmembrane orientations in dioleoylphosphatidylcholine (DOPC)and dilauroylphosphati
76 Dioleoylphosphatidylglycerol (DOPG), but not dioleoylphosphatidylcholine, exerted a similar inhibitor
77 regated, compacted DNA were formed by adding dioleoylphosphatidylcholine followed by removing the cho
78 ), a mixture of SM (sphingomyelin) and DOPC (dioleoylphosphatidylcholine) in their outer leaflets, an
79 oriented stacks and unilamellar vesicles of dioleoylphosphatidylcholine lipid bilayers to obtain the
80 Here, we describe melittin partitioning into dioleoylphosphatidylcholine lipids using CHARMM and OPLS
81 ace charge density of supported zwitterionic dioleoylphosphatidylcholine membranes with a variable fr
82 ds, dioleoylphosphatidylethanolamine (DOPE), dioleoylphosphatidylcholine, monooleoylglycerol, and cho
83 structure with binding constants relative to dioleoylphosphatidylcholine of 0.67 +/- 0.04 and 0.87 +/
84 ent when the receptor was reconstituted into dioleoylphosphatidylcholine or into a mixture of that li
85 with dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine, or a 1:1 mixture of these p
86 cholesterol, dipalmitoylphosphatidylcholine, dioleoylphosphatidylcholine, palmitoyloleoylphosphatidyl
87 when MscL is reconstituted into bilayers of dioleoylphosphatidylcholine runs from Leu-69 to Leu-92,
89 em of giant unilamellar vesicles composed of dioleoylphosphatidylcholine, sphingomyelin, and choleste
90 azole (IANBD) reconstituted into bilayers of dioleoylphosphatidylcholine varied with position, sugges
91 kbone amides of alamethicin reconstituted in dioleoylphosphatidylcholine vesicles by an exchange-trap
92 ystal structure of rat PITPbeta complexed to dioleoylphosphatidylcholine was determined to 2.18 A res
93 choline, dimyristoylphosphatidylcholine, and dioleoylphosphatidylcholine), we have modeled and simula
94 , composed of O-ethylphosphatidylcholine and dioleoylphosphatidylcholine, were labeled with a carbocy
95 composed of dioleoylphosphatidylglycerol and dioleoylphosphatidylcholine, were labeled with a rhodami