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1                                              DMPC (but not lecithin) raises HDL cholesterol and apoA-
2                                              DMPC in the form of small unilamellar vesicles (SUVs) or
3                                              DMPC or soy or egg lecithin at 1.0 mg/mL was added to th
4                                              DMPC-binding assays demonstrate an identical vesicle cle
5                                       At 1:1 DMPC:[1-44]apoA-I (w/w) ratio, discoidal complexes with
6 mixture, and the analog MG-H2 in DMPC or 3:1 DMPC/DMPG membranes.
7                         Consequently, apoC-1/DMPC disks are kinetically but not thermodynamically sta
8 e the apparent melting temperature of apoC-1:DMPC complexes by up to 20 degrees C and decelerate prot
9 ominant electrostatic interactions in apoC-1:DMPC disks are destabilizing.
10  density profiles of our simulations of 1024 DMPC lipids.
11 imately 5 [1-44]apoA-I and approximately 150 DMPC molecules per disk.
12 ed the expected interaction with ApoE(1-191).DMPC, but surprisingly CR16-18 did not interact with thi
13 16-18 variant capable of binding ApoE(1-191).DMPC.
14             However, in contrast to 2F in 2F.DMPC, 4F in the 4F.DMPC complex is located closer to the
15  betaCH(2) protons in 4F.DMPC, but not in 2F.DMPC, complex.
16  4F.DMPC complex is different than in the 2F.DMPC complex as evidenced by the NOE between lipid 2.CH
17              These NOEs are absent in the 2F.DMPC complex.
18 he conformation of the DMPC sn-3 chain in 4F.DMPC complex is different than in the 2F.DMPC complex as
19 ies to deduce detailed structure of 4F in 4F.DMPC discs.
20 tween lipid 2.CH and betaCH(2) protons in 4F.DMPC, but not in 2F.DMPC, complex.
21 , in contrast to 2F in 2F.DMPC, 4F in the 4F.DMPC complex is located closer to the lipid headgroup as
22 heptapeptide anchor (ANCH) in water and in a DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) bilay
23 ucture of the full-length H-ras protein in a DMPC bilayer has been computationally characterized.
24 ower coupling (14%) when the peptide is in a DMPC bilayer suggests a high degree of peptide conformat
25 cs of caveolin-1 (D82-S136; Cav182-136) in a DMPC bilayer using NMR, fluorescence emission measuremen
26        MD simulations, both in DMSO and in a DMPC bilayer, showed sites of local stability of helical
27 urther refined using molecular dynamics in a DMPC bilayer.
28                            A simulation in a DMPC/DMPG membrane did not lead to a stable pore, consis
29                              Although only a DMPC membrane was considered in this work, we speculate
30 he permeation of Na(+) and Cl(-) ions across DMPC lipid bilayer by computing the corresponding potent
31 MR spectra of MSI-78 in mechanically aligned DMPC bilayers.
32 the same polypeptide in mechanically-aligned DMPC and DOPC bilayers.
33                  The pattern of anchor amide-DMPC phosphate/carbonyl hydrogen bonds and the flexibili
34 reorganization are unfavorable, whereas ANCH-DMPC interactions-especially van der Waals-favor inserti
35 evidenced by a number of NOEs between 4F and DMPC headgroup protons.
36 hyl-ammonio]-1-propane sulfonate (Chaps) and DMPC/l-alpha-1,2-dihexanoyl-sn-glycero-3-phosphocholine
37 C and POPC or a further decrease in DLPC and DMPC bilayers.
38                                     DLPC and DMPC vesicles permitted rapid ion transfer across the bi
39 amic quantities characterizing pure DMPC and DMPC/cholesterol mixtures, thus directly confirming the
40 the volume expansion coefficient of DMPC and DMPC/Cholesterol samples with 13 and 25 mol% cholesterol
41 cs simulations of MAG2 performed in DMPC and DMPC/DMPG.
42  of DMPC, but the acyl chains in the EPL and DMPC bilayers occupy similar positions.
43 e of formation of rHDL from rcm apo A-II and DMPC at all FC mole percentages is faster than that of a
44 n the presence of both types of peptides and DMPC vesicles in the presence of nonselective peptides.
45 e aggregated in conventional DOPC, POPC, and DMPC membranes due to hydrophobic mismatch.
46 fect the BaP uptake rate by DMPC-NP-SLBs and DMPC-SUVs, indicating preferential BaP sorption into the
47  viability and growth using DMPC-NP-SLBs and DMPC-SUVs, with and without BaP, as their sole carbon so
48 on cooling from the heat-denatured state and DMPC clearance studies revealed that protein secondary s
49 -terminal lobe of LA5 in recognition of apoE-DMPC.
50 onolayers of ternary POPC/SM/Chol as well as DMPC/SM/Chol mixtures, which exhibit a surface-pressure-
51 probabilities for direct transitions between DMPC and DHPC were negligible, a third component with in
52 e as an intermediate for transitions between DMPC and DHPC.
53 quid crystalline medium, DMPC/DHPC bicelles (DMPC = dimyristoylphosphatidylcholine; DHPC = dihexanoyl
54 he dynamics and structure of edges formed by DMPC and palmitoyl-oleoylphosphatidylethanolamine.
55 nd compare it to that in a bilayer formed by DMPC/DMPA lipids.
56  and the orientation of water is governed by DMPC.
57                         Vesicles prepared by DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) and S
58 tter, does not affect the BaP uptake rate by DMPC-NP-SLBs and DMPC-SUVs, indicating preferential BaP
59 ing acyl chain length from 14 to 12 carbons (DMPC versus DLPC).
60                     These well-characterised DMPC/DHPC bicelles enable us to probe the influence of b
61  but was alpha-helical in negatively charged DMPC/DMPG vesicles.
62 ion we obtained an rHDL structure comprising DMPC, cholesterol, and apolipoprotein AI (423:74:1 mol/m
63 ce 13C was observed from bicelles containing DMPC and DHPC lipid molecules.
64 istoylphosphatidylcholine (d54-DMPC) and d54-DMPC/dimyristoylphosphatidylglycerol (DMPG) were used to
65 uterated dimyristoylphosphatidylcholine (d54-DMPC) and d54-DMPC/dimyristoylphosphatidylglycerol (DMPG
66  shorter tail component (either DDPC in DDPC/DMPC mixtures or DMPC in DMPC/DSPC mixtures) extending 2
67 ade NLPs from dimyristoylphospatidylcholine (DMPC) in combination with each of four different apolipo
68 c model of a dimyristoylphosphatidylcholine (DMPC) bilayer at various cholesterol concentrations via
69 zipper, in a dimyristoylphosphatidylcholine (DMPC) membrane.
70 ally aligned dimyristoylphosphatidylcholine (DMPC) bilayers.
71 s containing dimyristoylphosphatidylcholine (DMPC, di-C(14) tails) and dihexanoylphosphatidylcholine
72 line (DLPC), dimyristoylphosphatidylcholine (DMPC), dioleoylphosphatidylcholine (DOPC), and 1-palmito
73 tituted from dimyristoylphosphatidylcholine (DMPC) and human apolipoprotein C-I (apoC-I, 6 kDa) or it
74 tituted from dimyristoylphosphatidylcholine (DMPC) and selected mutants of human apolipoprotein C-1 (
75 idylcholine (dimyristoylphosphatidylcholine (DMPC) and palmitoyloleoylphosphatidylcholine (POPC)) and
76 porated into dimyristoylphosphatidylcholine (DMPC) bilayers.
77 id phases of dimyristoylphosphatidylcholine (DMPC) and dilauroylphosphatidylcholine (DLPC) were obtai
78  crystals of dimyristoylphosphatidylcholine (DMPC) and diphytanoylphosphatidylcholine (DPhPC), and th
79 mulations of dimyristoylphosphatidylcholine (DMPC) bilayers to model the creation of bilayer gaps-a c
80 ilization of dimyristoylphosphatidylcholine (DMPC) membranes by apo A-I to give rHDL increases as the
81 ilization of dimyristoylphosphatidylcholine (DMPC) multilamellar vesicles by apolipoprotein A-I (apoA
82 permeabilize dimyristoylphosphatidylcholine (DMPC) and dimyristoylphosphatidylglycerol (DMPG) vesicle
83 osed of pure dimyristoylphosphatidylcholine (DMPC) or palmitoyl-oleoylphosphatidylethanolamine (POPE)
84 n solubilize dimyristoylphosphatidylcholine (DMPC) liposomes and fold into approximately 60% alpha-he
85        Using dimyristoylphosphatidylcholine (DMPC) as a model lipid, these domains can convert multil
86 neously when dimyristoylphosphatidylcholine (DMPC) large unilamellar vesicles (LUVs) were incubated w
87 DeltaG1 with dimyristoylphosphatidylcholine (DMPC) and 1-palmitoyl-2-oleoyl-phosphatdylcholine bilaye
88 teracts with dimyristoylphosphatidylcholine (DMPC) over a wide range of lipid:peptide ratios from 1:1
89         With dimyristoylphosphatidylcholine (DMPC) phospholipid vesicles with 100 microM Ca (2+) pres
90 -PLA(2) with dimyristoylphosphatidylcholine (DMPC) vesicles and found that specific residues 113-120
91 zwitterionic dimyristoylphosphatidylcholine (DMPC) bilayer coincubated with calcium ions.
92  membrane-mimetic dimyristoylphosphocholine (DMPC) or 1-palmitoyl-2-oleoyl-sn-glycerophosphocholine (
93 anism of pore formation and closure in DLPC, DMPC, and DPPC bilayers, with pore formation free energi
94 ster than approximately 10(5) s(-1) in DLPC, DMPC, and POPC bilayers, but the motion is slowed by 2 o
95 P31) and the lipid hydrophobic length (DLPC, DMPC, and DPPC), a wide range of mismatch conditions wer
96 on and fluid phase bilayers formed from DMPG/DMPC and POPG/POPC mixtures.
97                                       Doping DMPC/DHPC bicelles with cholesterol sulfate broadens the
98 (m)): 41, 24, 7, and -20 degrees C for DPPC, DMPC, DLPC, and DOPC, respectively.
99 yers with different bilayer thickness, i.e., DMPC and POPC, the intramolecular distance reported by T
100 and 0.25 sterol mole fractions in ergosterol/DMPC mixtures.
101 m apolipoprotein AI, cholesterol, and excess DMPC and isolated to near homogeneity.
102  vesicles (SUVs) or DMPC-NP-SLBs with excess DMPC-SUVs to support colloidal stability, when added to
103 des areas per lipid A, 60.6 +/- 0.5 A(2) for DMPC and 63.2 +/- 0.5 A(2) for DLPC.
104 e has an area of 40.8 A(2) vs. 48.1 A(2) for DMPC.
105 lidate the new unilamellar vesicles data for DMPC, so method 4 is not required for DLPC or future stu
106 ept one of three independent simulations for DMPC and all three DLPC simulations, where the bilayer t
107 ta for the relative form factors F(q(z)) for DMPC were obtained using a combination of four methods.
108  coli polar lipids (EPLs), which differ from DMPC both in headgroups and acyl chains.
109 or shorter channels in liposomes formed from DMPC and for longer channels in DEPC.
110 this stoichiometry, apo A-II forms rHDL from DMPC and FC.
111  (w/v) phospholipid concentration and a high DMPC/DHPC ratio (q = 2.0) was found to be optimal for no
112 annel model was embedded in a fully hydrated DMPC lipid bilayer, and molecular-dynamics simulations w
113 mopentameric TM2 channel in a fully hydrated DMPC membrane using large-scale computation suggest a mo
114 complexes are similar to those of plasma A-I/DMPC complexes formed under similar conditions: small di
115              CD and EM studies of the apoA-I/DMPC complexes at different pH demonstrated that changes
116          Thermal unfolding of variant apoA-I/DMPC complexes monitored by circular dichroism (CD) show
117       A separate study was then conducted in DMPC liposomes in the presence of the putative membrane-
118 either DDPC in DDPC/DMPC mixtures or DMPC in DMPC/DSPC mixtures) extending 2-3 nm away from the prote
119 ces peptide-rich and peptide-poor domains in DMPC liposomes.
120              In contrast, spectra of GAsl in DMPC membranes indicate deeper embedding and tilt of the
121 ichiometric mixture, and the analog MG-H2 in DMPC or 3:1 DMPC/DMPG membranes.
122 havior of M2 transmembrane peptide (M2TM) in DMPC bilayers.
123 nal helix has a transmembrane orientation in DMPC bilayers, whereas in POPC bilayers, this domain is
124 R clearly indicates the presence of pairs in DMPC membranes.
125 ar-dynamics simulations of MAG2 performed in DMPC and DMPC/DMPG.
126 ssibly monomers and pentamers, is present in DMPC bilayers.
127 tra indicate that the presence of protein in DMPC results in a broad lipid phase transition that is s
128  that opsin can also be directly purified in DMPC/DHPC bicelles to give correctly folded functional o
129 ed M2 transmembrane peptide reconstituted in DMPC bilayers (38 degrees ).
130  of the on-time distributions of Nile Red in DMPC and SOPC vesicles were significantly different.
131 4 degrees (SKP in POPC), 22.3 degrees (SA in DMPC), and 31.7 degrees (SKP in DMPC).
132 grees (SA in DMPC), and 31.7 degrees (SKP in DMPC).
133 ly packed transmembrane melittin tetramer in DMPC shows formation of a toroidal pore after 1 mus.
134 ngle of 15 +/- 3 degrees in POPC, whereas in DMPC, 25 +/- 3 degree and 30 +/- 3 degree tilts were obs
135 ssociate with and dissociate from individual DMPC and SOPC vesicles adsorbed on a glass surface, gene
136 arkably, spontaneous insertion of BclXL into DMPC/DHPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine/1
137 t solution but can be directly purified into DMPC/Chaps.
138   Measurements of WALP19 in the ether-linked DMPC analogue ditetradecylphosphatidylcholine (missing t
139  different ratios of the zwitterionic lipid (DMPC, dimyristoyl phosphatidylcholine; DOPC, dioleoyl ph
140 ained in a single liquid crystalline medium, DMPC/DHPC bicelles (DMPC = dimyristoylphosphatidylcholin
141                                 In the mixed DMPC/DMPG bilayers, maculatin 1.1 induced DMPG phase sep
142                             Adding 1.0 mg/mL DMPC to the drinking water of 6-month-old apoE-null male
143 pid, these domains can convert multilamellar DMPC vesicles into discoidal-shaped particles.
144 nd a mutant form apoE4R158M to multilamellar DMPC vesicles was similar and was reduced and eventually
145  or the disk diameter among different mutant-DMPC complexes, the mutations have no significant effect
146 h an enhanced effect relative to the neutral DMPC bilayers.
147 hatidylcholine (egg PC) and is therefore not DMPC-dependent.
148 rent concentration on the phase behaviour of DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) multi
149     Here, supported phospholipid bilayers of DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) were
150 at the segmental order parameters (S(CD)) of DMPC approach very large values of approximately 0.35 in
151 ar vesicles indicate that the acyl chains of DMPC are highly disordered in the presence of the peptid
152 led that the volume expansion coefficient of DMPC and DMPC/Cholesterol samples with 13 and 25 mol% ch
153 econstituted vesicle dispersions composed of DMPC, C20BAS/E. coli polar lipid, C20BAS/POPC, C32phytBA
154 ptide bound to membrane bicelles composed of DMPC, DMPG, and DHPC, and compare it to the location of
155 in 1.2 in charged lipid bilayers composed of DMPC/DMPG.
156 rmotropic phase transition of MLVs formed of DMPC and the DMPC/DMPG (7:3) mixture suggests specific l
157 yer adjacent to the hydrophilic headgroup of DMPC.
158  of peptides interact with the headgroups of DMPC and DMPG bilayers.
159 Specifically, an aqueous phase incubation of DMPC vesicles with purified apolipoprotein A-I results i
160 of the experiment corresponds to the T(m) of DMPC, and domain boundaries between gel and liquid-cryst
161  model is then extended to treat mixtures of DMPC and cholesterol, where small domains of different c
162  simulations for several bilayer mixtures of DMPC and cholesterol.
163                          Adding 1.0 mg/mL of DMPC to the drinking water of 10-month-old apoE-null fem
164 ave no significant effect on the ordering of DMPC acyl chains.
165 -fusion inhibitor, decreased the ordering of DMPC headgroups, whereas arachidonic acid, a membrane-fu
166 e-fusion promoter, increased the ordering of DMPC headgroups.
167 erface (for example, >43% in the presence of DMPC).
168 in the bicelle size and, thus, proportion of DMPC bilayer present.
169 c ring system with increasing proportions of DMPC in the bicelle preparation.
170                                  The rate of DMPC microsolubilization by apoA-I is highly dependent u
171 able basis for their effects on the rates of DMPC microsolubilization.
172 to be modulated by the q value, the ratio of DMPC to DHPC, which reflects changes in the bicelle size
173 ated with a slower rate of solubilization of DMPC vesicles by apoE4-mut1 and reduced binding of the p
174  concentration, and the lipid phase state of DMPC, the kinetics varied over 3 orders of magnitude.
175  this temperature becomes similar to that of DMPC.
176 eract differently with AQP0 than do those of DMPC, but the acyl chains in the EPL and DMPC bilayers o
177  complexes rising more steeply than those of DMPC/DMPG-peptide complexes.
178                      The phase transition of DMPC shifted from 23.4 degrees C toward lower temperatur
179 nergy of 220 kJ/mol for the translocation of DMPC, DPPC, and DSPC was determined.
180 rbidity clearance of unilamellar vesicles of DMPC, is faster at acidic pH values and consistent with
181 a-helical content in solution (0-48%) and on DMPC (40-75%).
182 otein secondary structure in solution and on DMPC correlates strongly with the maximal temperature of
183 pha-helical content in solution (33%) and on DMPC disks (67%) similar to that of the wild type (WT),
184 roteins with higher alpha-helical content on DMPC may form more stable complexes.
185           Furthermore, 2H NMR experiments on DMPC-d54 multilamellar vesicles indicate that the acyl c
186 ponent (either DDPC in DDPC/DMPC mixtures or DMPC in DMPC/DSPC mixtures) extending 2-3 nm away from t
187 ituted into a TFE/H(2)O mixture or a POPC or DMPC bilayer were estimated to be 10.6 +/- 0.5, 16.8 +/-
188 form of small unilamellar vesicles (SUVs) or DMPC-NP-SLBs with excess DMPC-SUVs to support colloidal
189 labeled peptides was carried out in oriented DMPC bilayers.
190 nvironment, namely, macroscopically oriented DMPC:DHPC bicelles.
191 ep and immediate weakening, whereas the P294-DMPC binding was slightly strengthened at pH 3.7 and the
192                  As the pH was lowered, P326-DMPC binding had a steep and immediate weakening, wherea
193 egrees C did not cause colour change in PCDA/DMPC vesicles for a period of up to 60days of storage.
194                               In fluid-phase DMPC bilayer systems, the peptides interacted primarily
195 e in membrane fluidity between the gel phase DMPC and the liquid crystal phase POPC for peptide-membr
196 -disruptive effect is enhanced for gel phase DMPC membranes.
197 tron density profiles with that of gel phase DMPC provides areas per lipid A, 60.6 +/- 0.5 A(2) for D
198                                 In gel-phase DMPC vesicles, the native peptide disrupted the bilayer
199 imyristoyl-sn-glycero-3-phosphatidylcholine (DMPC) bilayers at various temperatures.
200 imyristoyl-sn-glycero-3-phosphatidylcholine (DMPC).
201 imyristoyl-sn-glycero-3-phosphatidylcholine (DMPC)/1,2-dimyristoyl-sn-glycero-3-phosphatidylglycerol
202 icelle or a dimyristoyl phosphatidylcholine (DMPC) bilayer, have been used to explore the conformatio
203 (AQP0) with dimyristoyl phosphatidylcholine (DMPC) lipids.
204 plexes with dimyristoyl phosphatidylcholine (DMPC) that resemble nascent HDL were analyzed by density
205  binding to dimyristoyl phosphatidylcholine (DMPC) vesicles and to triglyceride (TG)-rich emulsion pa
206 apoC-1) and dimyristoyl phosphatidylcholine (DMPC).
207 an explicit dimyristoyl-phosphatidylcholine (DMPC) lipid bilayer.
208 hospholipid dimyristoyl-phosphatidylcholine (DMPC) the two-state model was sufficient to account for
209 1)) and 1,2-dimyristoyl-phosphatidylcholine (DMPC-d(54)) at different temperatures demonstrates the i
210 yristoyl or dipalmitoyl phosphatidylcholine (DMPC or DPPC), the latter without or with cholesterol, w
211 myristoyl-sn-glycero-3-phosphatidylcholine] (DMPC) interface in the OH stretching mode region of wate
212 ids dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DH
213 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DH
214 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and its mixtures with different amounts of cholest
215 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and POPC/POPS 3:1 liposomes retain a bilayer macro
216 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) are investigated as constructs for removing PAHs f
217 h a 1,2-dimyristoylglycero-3-phosphocholine (DMPC) bilayer obtained from modeling and all-atom explic
218 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) bilayers in the presence of MSI-78 provides images
219 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) bilayers, the first equivalent of drug bound S31 i
220 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a phospholipid that does not exist in nature an
221 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) liposomes, suggesting that lateral gating of the B
222 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) vesicles and dodecylphosphocholine (DPC) micelles
223 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC)) and phosphatidylglycerols (PGs, such as 1,2-dimyr
224 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC),
225 -dimyristoleoyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC),
226 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC
227 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC
228 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC).
229 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC).
230 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC)/1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)
231 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC)/3-[(cholamidopropyl)dimethyl-ammonio]-1-propane su
232 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC:DSPC).
233 f 1,2-dimyristoyl-sn-glycero-phosphocholine, DMPC) and the bacterial (liposomes of 1,2-dimyristoyl-sn
234  out in explicit lipid bilayers (DEPC, POPC, DMPC, sphingomyelin), confirming the observed dependence
235 that decreasing bilayer thickness (DEPC-POPC-DMPC) led to an increase in the helix tilt angle from 10
236        These bicelles are thought to provide DMPC bilayer fragments with most DHPC capping the bilaye
237  of the bilayer is similar to that of a pure DMPC, there are localized perturbations.
238 thermodynamic quantities characterizing pure DMPC and DMPC/cholesterol mixtures, thus directly confir
239 r (GlyR) was achieved in low-q bicelles (q = DMPC/DHPC).
240 iscriminating between different modes of ras-DMPC interactions.
241 markedly increased in the mice that received DMPC.
242 ere increased 2- to 3-fold in mice receiving DMPC but not soy or egg lecithin.
243  dramatically improved in the mice receiving DMPC, and there was a significant reduction in aortic le
244 25-50% anionic lipids, and in both saturated DMPC/DMPG (1,2-dimyristoyl-sn-glycero-3-phosphatidylchlo
245 e simulated an excess proton near a solvated DMPC bilayer at 323 K, using a recently developed method
246 lateral mobility of globular actin-supported DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) bilay
247 observed magainin interacting with synthetic DMPC/DMPG membranes.
248                                    We tested DMPC in vivo in apolipoprotein (apo) E-null mice.
249 eraction with the protein or by altering the DMPC/Chaps bilayer properties within the bicelle.
250 ns between the H-ras membrane anchor and the DMPC bilayer are investigated in detail.
251 teraction between these Trp residues and the DMPC interfacial region.
252 se transition of MLVs formed of DMPC and the DMPC/DMPG (7:3) mixture suggests specific lipid-peptide
253  form is just long enough to wrap around the DMPC bilayer disk once.
254 ne tension of approximately 10-30 pN for the DMPC edge, in qualitative agreement with experimental es
255 r, transition peak has been observed for the DMPC: cholesterol mixtures suggest that a separate chole
256                                       In the DMPC bilayer, the hydrophobic component dominates, regar
257 reduction in aortic lesions (P=0.021) in the DMPC mice but not in those receiving lecithin.
258 )) are 0.3 and 0.73 G for the peptide in the DMPC or POPC bilayer environment, respectively.
259 e inclusion of Chaps rather than DHPC in the DMPC/Chaps bicelles, however, imparts the greatest stabi
260        This suggests that it is not just the DMPC bilayer fragment in the bicelles that stabilises th
261 volves two factors: 1) calcium ions make the DMPC bilayer partially cationic and thus attractive to t
262 cal thinning and 2 A average thinning of the DMPC (1,2-dimyristoyl-sn-glycero-3-phosphochloline)/DMPG
263 phodiester groups in the two leaflets of the DMPC and EPL bilayers is almost identical.
264 ich matches the hydrophobic thickness of the DMPC bilayer.
265                Using kinetic analysis of the DMPC clearance assay, we show that the identified phosph
266   Interestingly, at Tc = 24 degrees C of the DMPC gel-to-liquid crystal transition, the clearance rat
267         In addition, the conformation of the DMPC sn-3 chain in 4F.DMPC complex is different than in
268 his cholesterol concentration is reached the DMPC-rich domain disappears.
269   According to turbidimetric titrations, the DMPC/apo A-II stoichiometry is 65/1 (moles to moles).
270 ium strengthens Abeta peptide binding to the DMPC bilayer by enhancing electrostatic interactions bet
271                                    While the DMPC chains were longer than DLPC with a correspondingly
272 te cholesterol rich domain coexists with the DMPC rich domain.
273  investigated using thicker POPC and thinner DMPC bilayers.
274 peptide is more heterogeneous in the thinner DMPC bilayer than in the thicker POPC bilayer.
275                                        Thus, DMPC binding may not substantially increase the low appa
276  model in which apo A-I and apo A-II bind to DMPC via surface defects that disappear at 20 mol % FC.
277 lipid-protein domains upon apoA-I binding to DMPC LUVs.
278 scopy demonstrated that the peptide binds to DMPC with a high affinity to form at least two sizes of
279                                When bound to DMPC, [1-44]apoA-I has approximately 60% helical structu
280 ises from the near-bulk water nonadjacent to DMPC.
281 g of the drug molecules in optically trapped DMPC vesicles, the membrane permeability and partitionin
282 inosa demonstrate viability and growth using DMPC-NP-SLBs and DMPC-SUVs, with and without BaP, as the
283  not possible with the previous method using DMPC vesicles.
284              We previously reported on using DMPC (dimyristoylphosphatidylcholine) vesicles for reali
285 bility, the initial rate of association with DMPC liposomes, and the size of the rHDL particles.
286            We propose that apoA-I binds with DMPC LUVs to form small lipid-protein domains on the LUV
287 ion of residues in the catalytic domain with DMPC phosphates.
288 ed amantadine, an antiinfluenza A drug, with DMPC bilayers were investigated by solid-state NMR and b
289         The reaction kinetics of apoA-I with DMPC LUVs was monitored by fluorescence resonance energy
290 ow that LL7-27 is completely integrated with DMPC/DMPG (3:1) liposomes, but induces peptide-rich and
291  LUV and a half-life time around 10 min with DMPC SUV.
292 teractions of single Nile Red molecules with DMPC and SOPC lipid bilayers were studied by single mole
293 , apo A-II, like apo A-I, reacts poorly with DMPC containing >/=20 mol % FC.
294 ion of gramicidin D at a 1:20 mol ratio with DMPC results in the formation of protein-lipid hydrogen
295 yl-sn-glycero-3-phosphocholine (DHPC), with [DMPC]/[DHPC] = 2.5, in 10% lipid/aqueous buffer at 25 de
296 alpha-helix content (40%) compared to the WT-DMPC disks (65%).
297 er, <d> = 13 nm, compared to 17 nm of the WT-DMPC disks.
298 elles, and TM2 was disordered in zwiterionic DMPC but was alpha-helical in negatively charged DMPC/DM
299 showed much weaker affinity for zwitterionic DMPC, but had moderate binding affinity to negatively ch
300 negatively charged DMPG than to zwitterionic DMPC.

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