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1 general destabilization and leakiness of the lipid bilayer membrane.
2 istoyl group, enabling it to interact with a lipid bilayer membrane.
3 s through a 2.6-nm diameter ion channel in a lipid bilayer membrane.
4 from their different localization within the lipid bilayer membrane.
5 cells, with a size range of 40-150 nm and a lipid bilayer membrane.
6 biotin capture surface based on a supported lipid bilayer membrane.
7 al acto-myosin network linked to a supported lipid bilayer membrane.
8 ne triphosphatases in an integrated in vitro lipid bilayer membrane.
9 way when it is added to only one side of the lipid bilayer membrane.
10 f varying hydrophobicity as well a supported lipid bilayer membrane.
11 ut on both structures embedded in a solvated lipid bilayer membrane.
12 ges in the concentration of cations near the lipid bilayer membrane.
13 oxidase in the electrode-supported thiolipid/lipid bilayer membrane.
14 R/Ca2+ release channel incorporated into the lipid bilayer membrane.
15 within nanopores and biological channels in lipid bilayer membranes.
16 mall peptide, penetratin, to solid-supported lipid bilayer membranes.
17 the barrel-stave model for pore formation in lipid bilayer membranes.
18 or metal ion coordination self-organize into lipid bilayer membranes.
19 oring of the translocation of COSANs through lipid bilayer membranes.
20 protein secondary structure and topology in lipid bilayer membranes.
21 ngle OmpF channels reconstituted into planar lipid bilayer membranes.
22 tide libraries for members that permeabilize lipid bilayer membranes.
23 dded, frozen-hydrated 2D crystals of AQP1 in lipid bilayer membranes.
24 ization by tPMP-1 by using artificial planar lipid bilayer membranes.
25 ubule membranes and incorporated into planar lipid bilayer membranes.
26 ptide forms ion-permeable channels in planar lipid bilayer membranes.
27 miting steps for transport of FA across pure lipid bilayer membranes.
28 tor (CFTR) chloride channel reconstituted in lipid bilayer membranes.
29 brane vesicles for reconstitution studies in lipid bilayer membranes.
30 on the physical properties of intracellular lipid bilayer membranes.
31 cular machinery, including ion pumps, within lipid bilayer membranes.
32 e resultant nanoparticles through cell-based lipid bilayer membranes.
33 measure stages of phase separation in model lipid bilayer membranes.
34 ures that control molecular transport across lipid bilayer membranes.
35 pid-exposed His, Lys, and Arg side chains in lipid bilayer membranes.
36 exposed directly to lipid acyl chains within lipid bilayer membranes.
37 ctive Cl(-) ion binding and transport across lipid bilayer membranes.
38 troduced as ideal to transport anions across lipid bilayer membranes.
39 readily intercalates into model and natural lipid bilayer membranes.
40 be functionally reconstituted into synthetic lipid bilayer membranes.
41 tments and separated from the environment by lipid bilayer membranes.
42 ty to interact with the interfacial zones of lipid bilayer membranes.
43 lt angles that span 5 degrees -35 degrees in lipid bilayer membranes.
44 hermore adopt a moderate average tilt within lipid bilayer membranes.
45 g purified receptors inserted into deposited lipid bilayer membranes.
46 f chalcogen bonds to transport anions across lipid bilayer membranes.
47 d to study the mechanical properties of soft lipid bilayer membranes.
48 f-organizing physical dynamics of biological lipid-bilayer membranes.
49 y reported to permeate by themselves through lipid bilayer membranes, a propensity that is related to
51 synthetic signal transducer embedded in the lipid bilayer membrane acts as a switchable catalyst, ca
52 nanopore from the cis to the trans side of a lipid bilayer membrane, allowed to refold and interact w
53 the transverse and lateral structures of the lipid bilayer membrane, along with a description of lipi
54 eter-sized magnetic crystals surrounded by a lipid bilayer membrane and organized into chains via a d
55 in water and a dipalmitoylphospatidylcholine lipid bilayer membrane and to the free energies of solut
56 tally by reconstitution assays with actin on lipid bilayer membranes and provide a molecular-level un
57 els' transport performances were assessed in lipid bilayer membranes, and the channels were able to t
58 verse structure and regulated deformation of lipid bilayer membranes are among a cell's most fascinat
62 This work points to new prospects for using lipid bilayer membranes as scaffolds for confining, orie
64 ence or absence of an envelope composed of a lipid-bilayer membrane, attributes that profoundly affec
65 rease the specific conductance of artificial lipid bilayer membranes by the formation of ion-permeabl
66 th a length comparable to the thickness of a lipid bilayer membrane can self-insert into the membrane
68 r self-association and enhanced affinity for lipid bilayer membranes, compared to the wild-type pepti
69 tions of cholesterol and alpha-tocopherol on lipid bilayer membranes composed of different phosphatid
71 sfer to proton translocation across a closed lipid bilayer membrane, conserving the free energy relea
72 molecular dynamics computer simulation of a lipid bilayer membrane consisting of cholesterol and 1-s
73 ing peptide, penetratin, and solid-supported lipid bilayer membranes consisting of either egg phospha
74 , molecular dynamics simulations of hydrated lipid bilayer membranes containing highly polyunsaturate
80 nted for samples of 1) oriented diI in model lipid bilayer membranes, erythrocytes, and macrophages;
81 in which transporters on opposite sides of a lipid bilayer membrane facilitate transport by passing i
82 len 1 to pyranine, its impermeability to the lipid bilayer membrane, fast kinetics of binding, and ab
84 yringomycin E, when incorporated into planar lipid bilayer membranes, forms two types of channels (sm
86 dsorbed on magnetic ZnO particles bound by a lipid bilayer membrane from Caco-2 cells (human colorect
87 icin reconstituted into an artificial planar lipid bilayer membrane from the point of view of electri
88 beta-sheet aggregates upon partitioning into lipid bilayer membranes from the aqueous phase where the
89 ining the delta exon5 CFTR proteins into the lipid bilayer membrane, functional phosphorylation- and
90 spect to the membrane normal of DOPC or DPPC lipid bilayer membranes, GWALP23-R14 shows one major sta
91 stributed actin network interacting with the lipid bilayer membrane have been assumed to control RBC
92 o measure transmembrane-protein diffusion in lipid bilayer membranes have advanced in recent decades,
93 ugged channels in an ion-conducting state in lipid bilayer membranes have so far been unsuccessful.
94 raft hypothesis postulates the existence of lipid bilayer membrane heterogeneities, or domains, supp
95 The highly anisotropic environment of the lipid bilayer membrane imposes significant constraints o
96 re we include explicit H(2)O and an infinite lipid bilayer membrane in molecular dynamics (MD) simula
100 nd reproducible method to form free-standing lipid bilayer membranes in microdevices made with Norlan
101 naling proteins transduce information across lipid bilayer membranes in response to extra-cellular bi
102 mselves into, and at least partially across, lipid bilayer membranes in the absence of any auxiliary
103 of the skeleton attachment to the fluidlike lipid bilayer membrane, including a specific accounting
104 Platinum microelectrodes are modified with a lipid bilayer membrane incorporating cholesterol oxidase
105 Nanoscale structural reorganization of a lipid bilayer membrane induced by a chemical recognition
107 o dome is expected to deform the surrounding lipid bilayer membrane into a membrane footprint, which
109 ng the nanoscale dynamic organization within lipid bilayer membranes is central to our understanding
110 Controlled transport of biomolecules across lipid bilayer membranes is of profound significance in b
111 and amplification of chemical signals across lipid bilayer membranes is of profound significance in m
112 hemical information between cells and across lipid bilayer membranes is of profound significance in m
113 donor and acceptor molecules in two apposing lipid bilayer membranes is used to resolve topographical
114 y its interactions with a rigid more ordered lipid bilayer membrane, is regulated in plasma membranes
115 rates that peptide 1a interacts with anionic lipid bilayer membranes, like oligomers of full-length a
117 enveloped virus particles (those that lack a lipid-bilayer membrane) must breach the membrane of a ta
120 el biophysical insight into the influence of lipid bilayer membranes on conformer preferences and con
121 f the bellflower model demonstrate that in a lipid bilayer membrane or a detergent micelle, the cytop
122 n of Ca2+-ATPase involves PLN monomers, in a lipid bilayer membrane, PLN monomers form stable pentame
124 (4)) or greigite (Fe(3)S(4)), enveloped by a lipid bilayer membrane, produced by magnetotactic bacter
125 isolated mitochondrial proteins, and planar lipid bilayer membranes reconstituted with recombinant p
126 f transport of free fatty acids (FFA) across lipid bilayer membranes remains a subject of debate.
128 s isolated from these transfected cells into lipid bilayer membrane resulted in single Ca(2+) release
130 with structures determined experimentally in lipid bilayer membranes show that eefxPot affords signif
131 contact between the electrode and a vesicle lipid bilayer membrane shows a response that correlates
132 lecular dynamics simulation with an explicit lipid bilayer membrane, similar to the system used for t
133 terol labeled cages on spherically supported lipid bilayer membranes (SSLBM) formed on silica beads,
134 ribution within synthetic cells comprising a lipid bilayer membrane surrounding an aqueous polymer so
136 ly to microscropically unresolvable rafts in lipid bilayers, membrane tension led to the appearance o
137 d trianglamine macrocycles acting as AWCs in lipid bilayer membranes that are able to transport water
138 ryotic counterparts, which are surrounded by lipid bilayer membranes, these microbial organelles are
141 lease cytochrome c and to destabilize planar lipid bilayer membranes through reduction of pore line t
144 all mammalian cells is the adherence of the lipid bilayer membrane to the underlying membrane associ
147 fication techniques to form myelin-mimicking lipid bilayer membranes to measure both the association
148 ence or absence of an envelope - an external lipid bilayer membrane typically carrying one or more vi
150 sensitive (MS) channel gated by tension in a lipid bilayer membrane under stresses due to fluid flows
152 Extracellular vesicles are cell-originated lipid bilayer membrane vesicles that play vital roles in
153 ntly compared to SO(4)(2-) anions across the lipid bilayer membrane via a mobile carrier mechanism.
154 droxyl groups within the hydrocarbon core of lipid bilayer membranes, we examined the structural and
155 iport mechanism and channel formation in the lipid bilayer membranes were confirmed for the most acti
156 gth of COE-CN leads to weaker binding within lipid bilayer membranes, which allows sampling of intern
157 cells is known to be supplied by both their lipid bilayer membranes, which resist bending and local
158 in dramatically increases the conductance of lipid bilayer membranes, while non-cytotoxic rat amylin
159 P(2) molecules within the inner leaflet of a lipid bilayer membrane with possible binding sites on Ki
160 alysis reveals the transport of water across lipid bilayer membranes with a relative water permeabili