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1 polypeptides that interact with a supported lipid bilayer.
2 often depends on their interactions with the lipid bilayer.
3 of free acyl coenzyme A (acyl-CoA) from the lipid bilayer.
4 at human Na(V)1.7 and their affinity for the lipid bilayer.
5 multiple molecular components, including the lipid bilayer.
6 from spiders that has weak affinity for the lipid bilayer.
7 s hydrophobic transmembrane helices into the lipid bilayer.
8 ty is the formation of pores in the membrane lipid bilayer.
9 stem where motors were linked to a supported lipid bilayer.
10 binding, aggregation, and insertion into the lipid bilayer.
11 nding site via lateral diffusion through the lipid bilayer.
12 ane helices IV and V that connects it to the lipid bilayer.
13 ane is remarkable; it is a highly asymmetric lipid bilayer.
14 mers by NMR in bicelles that closely mimic a lipid bilayer.
15 are closest to the extracellular face of the lipid bilayer.
16 angle of tilt of the GPCR in the surrounding lipid bilayer.
17 a complex and deposited on a mica-supported lipid bilayer.
18 e crystal structures embedded in an explicit lipid bilayer.
19 ng Abeta fragment Abeta25-35 within the DMPC lipid bilayer.
20 cting linker in a complete model of AE1 in a lipid bilayer.
21 llenging to characterize structurally in the lipid bilayer.
22 ion of transmembrane domains (TMDs) into the lipid bilayer.
23 acids and their proximity with the supported lipid bilayer.
24 sed it to study vesicle fusion to a tethered lipid bilayer.
25 m and is connected to its neighbor through a lipid bilayer.
26 binding in a more natural and detergent-free lipid bilayer.
27 ts of the bulky transport domain through the lipid bilayer.
28 -covalent, hydrophobic interactions with the lipid bilayer.
29 eals that the C-edge of betaarr1 engages the lipid bilayer.
30 oyl-sn-glycero-3-phosphocholine (DC(18:1)PC) lipid bilayer.
31 om the OF transporter and partition into the lipid bilayer.
32 beta(1-42) fragments that were closer to the lipid bilayer.
33 ging because of difficulties in modeling the lipid bilayer.
34 sensing mechanical force transmitted via the lipid bilayer.
35 equire the presence of cholesterol to pierce lipid bilayers.
36 reported for membrane proteins in supported lipid bilayers.
37 small unilamellar vesicles (SUVs) and planar lipid bilayers.
38 act with or alter the physical properties of lipid bilayers.
39 physical phenomena like phase separation in lipid bilayers.
40 that had previously been shown to fuse with lipid bilayers.
41 f negative pressures in liquids that contain lipid bilayers.
42 or channel formation and pH gating in planar lipid bilayers.
43 fector complex Rabex5/Rabaptin5 on supported lipid bilayers.
44 channels but perturb the local properties of lipid bilayers.
45 label-free chemically specific microscopy of lipid bilayers.
46 tation of molecules assembled into nanoscale lipid bilayers.
47 n RyR2 channels incorporated into artificial lipid bilayers.
48 s of defined compositions, to form supported lipid bilayers.
49 itates the insertion of single RHPs into the lipid bilayers.
50 ength constructs on reconstituted, supported lipid bilayers.
51 e rate, k(F), for two different peptides and lipid bilayers.
52 anes, except P#8, which was designed to span lipid bilayers.
53 ates in the stalks formed between 2 opposing lipid bilayers.
54 ving cells (human and Drosophila) and planar lipid bilayers.
55 to observe spontaneous gA dimer formation in lipid bilayers.
56 nely research biological membranes, not just lipid bilayers.
57 and multi-span membrane proteins embedded in lipid bilayers.
58 characterize AMP oligomeric complexes within lipid bilayers.
59 des and membrane proteins embedded in intact lipid bilayers.
60 f different isolated Abeta assembly types on lipid bilayers.
61 ngle RyR1 channels reconstituted into planar lipid bilayers.
62 lic particles smaller than 6 nm can embed in lipid bilayers.
63 vidual bacteriorhodopsin molecules in native lipid bilayers.
64 re in their in vivo orientation within fluid lipid bilayers.
65 actin in the vicinity of differently charged lipid bilayers.
66 about cholesterol complexation with gp41 in lipid bilayers.
67 smembrane channels in cholesterol-containing lipid bilayers.
68 n vitro potency at Na(V)1.7 and affinity for lipid bilayers.
69 nel recording of RyR2 activity in artificial lipid bilayers.
70 s and MAG are not presented as part of fluid lipid bilayers.
71 ractions contribute to lateral clustering on lipid bilayers.
72 mains resembling the morphology of supported lipid bilayers.
73 dependent conformational dynamics of MdfA in lipid bilayers.
74 form of alphaS and modulates the binding to lipid bilayers.
75 y in lipids, especially near the midplane of lipid bilayers.
77 ting modifier toxins have affinity for model lipid bilayers, a tripartite relationship among gating m
78 membrane at nanoneedle sites shows an intact lipid bilayer, accompanied by an accumulation of clathri
79 ic surface profile, which displays increased lipid bilayer affinity and in vitro activity at the volt
80 lypeptide mimics of mucins and added them to lipid bilayers, allowing chemical control of length, gly
81 econstituting an OmpF porin in an artificial lipid bilayer and applying an electric field across it,
83 t-simulating an entire mammal red blood cell lipid bilayer and cytoskeleton as modeled by multiple mi
84 y to form low order oligomers on a supported lipid bilayer and that neither membrane association nor
85 tions to maximise protein integration into a lipid bilayer and the oligomerisation of the protein int
86 lar dynamics (MD) simulations in an explicit lipid bilayer and water environment (1.6 million atoms i
87 loid beta (Abeta42) induce the disruption of lipid bilayers and an inflammatory response to different
88 membrane protein W have been investigated in lipid bilayers and detergent micelles by solution NMR re
89 ory module also phase-separates on supported lipid bilayers and forms dynamic foci when expressed het
91 s, we determined that PlsX binds directly to lipid bilayers and identified its membrane anchoring moi
92 s into the lipid-lipid interactions in model lipid bilayers and improve our understanding of the late
93 nt of molecular dynamics (MD) simulations of lipid bilayers and membrane proteins, including aquapori
94 the sponge phase contains a dense network of lipid bilayers and nanometric aqueous channels, which al
95 that consist of a protein belt surrounding a lipid bilayer, and are broadly used for characterization
96 nshielded hydrophilic side chains within the lipid bilayer, and it disengages concomitant with substr
97 ing the de novo NMR structure in near-native lipid bilayers, and by accessing structural dynamics rel
98 e-channel conductance measurements in planar lipid bilayers, and in vivo fluorescence imaging, we dem
99 ins form water-filled nanoscale pores within lipid bilayers, and their properties are dependent on th
100 fully preserve the biophysical properties of lipid bilayers, and therefore, questions on binding spec
102 hedra (MOP) and their biomimetic coatings of lipid bilayers are described to synergistically combine
104 ect interactions between actin filaments and lipid bilayers are possible and that the net charge of t
105 Then molecular dynamics (MD) simulations in lipid bilayers are used to pinpoint likely lipid-protein
106 c, electrical, and rheological properties of lipid bilayers as a function of membrane composition, su
109 ipeline was developed to allow the automated lipid bilayer assembly around new membrane protein struc
110 nd exhibit selective proton transport across lipid bilayers at a rate similar to those of natural pro
111 n that recombinant APOL1 inserts into planar lipid bilayers at acidic pH to form pH-gated nonselectiv
112 omistic simulations to be highly flexible in lipid bilayers at ambient temperature, with large rockin
113 ort of individual substrate molecules across lipid bilayers at both single- and multi-turnover resolu
114 lycan layer only to find another hydrophobic lipid bilayer before it finally enters the cytoplasm, wh
116 vestigate the influence of small solutes and lipid bilayers, both constituents of all biological liqu
118 a is reported to have various impacts on the lipid bilayer, but a clearer picture of Abeta influence
119 a collapsed conformation at the level of the lipid bilayer, but we observed a large, hydrophilic and
120 etermine quantitatively its association with lipid bilayers by means of scanning fluorescence correla
123 poration of the same preparation into planar lipid bilayers Ca(2+) elicits currents matching those of
124 ne proteins with respect to the plane of the lipid bilayer can be largely determined by membrane lipi
126 n and, uniquely, physical transformations of lipid bilayers can be monitored on a length scale of mic
129 he first time that the chiral environment of lipid bilayers can modulate the function of membrane-act
132 ity and curvature constraints imposed on the lipid bilayer components of the cell membrane are the ma
133 orces on membrane molecules propagate to the lipid bilayer components to generate specific nanomechan
135 control anomalous diffusion using supported lipid bilayers containing lipids derivatized with polyet
137 n Alzheimer's disease that the disruption of lipid bilayers correlates linearly with the time course
138 A) ion channels embedded in planar suspended lipid bilayers demonstrate that anionic gold nanoparticl
139 e effects of tacrolimus on purified TRPM8 in lipid bilayers demonstrates conclusively that it has a d
140 enza virus is an RNA virus encapsulated in a lipid bilayer derived from the host cell plasma membrane
141 water-soluble fluorophores to interact with lipid bilayers, detailed fluorophore-lipid interactions
142 rmation and the backbone hydrogen bonding in lipid bilayers differ from the micelle-bound conformatio
143 nical force alters the physical state of the lipid bilayer, driving mechanosensors to assume conforma
144 suggesting that physical deformation of the lipid bilayer, either by mechanical force or curvature,
145 e postspike pore follows from predictions of lipid bilayer elasticity and offers an explanation for p
147 port kinetics measurements, the lifetimes of lipid bilayer electropores were measured using systemati
152 ent membrane proteins for native MS within a lipid bilayer environment, but previous native MS of mem
155 h the lipid and C(18) alkyl chains of hybrid lipid bilayers evolve during deposition and organization
158 end to protrude through the enzyme into the lipid bilayer, facilitating the desaturation of very-lon
160 e made by coating glass beads with supported lipid bilayers followed by coupling proteins and other l
163 membrane permeability P(ion) through planar lipid bilayers for six PFAAs and three alternatives.
165 ies on the phase behaviour of multicomponent lipid bilayers found an intricate interplay between memb
166 s 2 (SARS-CoV-2) virions are surrounded by a lipid bilayer from which spike (S) protein trimers protr
167 to display the predicted MPs embedded in the lipid bilayer guided by the predicted transmembrane topo
169 r physiochemical properties, nucleosides are lipid bilayer impermeable and thus rely on dedicated tra
170 he cell builds and maintains this asymmetric lipid bilayer in coordination with the assembly of the o
173 e association of small molecules with hybrid-lipid bilayers in C(18) chromatographic silica particles
174 ingle-channel electrical recording in planar lipid bilayers in conjunction with protein engineering,
175 eous pre-gel droplets were connected through lipid bilayers in predetermined architectures and photop
178 ciples might have relevance for conventional lipid bilayers, in which the assembly of higher-order st
180 main of the influenza A M2 proton channel in lipid bilayers increases dramatically at an elevated pro
181 the Nephrin-Nck-N-WASP signaling pathway on lipid bilayers increases membrane dwell time of N-WASP a
185 Whereas lateral movement of proteins in this lipid bilayer is possible, it is rather limited in turgi
186 e BsYetJ (or TMBIM6) structure embedded in a lipid bilayer is uncharacterized, let alone the molecula
190 owding, emulated by the PEG molecules at the lipid bilayer, is enough to promote the polymerization o
193 stributed actin network interacting with the lipid bilayer membrane have been assumed to control RBC
194 (4)) or greigite (Fe(3)S(4)), enveloped by a lipid bilayer membrane, produced by magnetotactic bacter
196 tally by reconstitution assays with actin on lipid bilayer membranes and provide a molecular-level un
197 and amplification of chemical signals across lipid bilayer membranes is of profound significance in m
198 isolated mitochondrial proteins, and planar lipid bilayer membranes reconstituted with recombinant p
207 f the explanations for mechanosensitivity, a lipid-bilayer model, suggests that a stretch of the memb
209 cholesterol = 0.39/0.39/0.22 and a supported lipid bilayer of 1,2-dioleoyl-sn-glycero-3-phosphocholin
211 release of the protein precursor within the lipid bilayer of the inner membrane, followed by cleavag
212 We suggest that the BCR forms within the lipid bilayer of the membrane a symmetric Igalpha-mHC:mH
214 s studied on fluorescently labeled supported lipid bilayers of different lipid compositions at mechan
215 ect odorant receptors reconstituted into the lipid bilayers of liposomes can be successfully immobili
216 12A, stains exclusively the outer leaflet of lipid bilayers of liposomes, as evidenced by leaflet-spe
218 free energy by drug-induced perturbations of lipid bilayer physical properties and bilayer-gramicidin
220 using approaches that include the supported lipid bilayer platform as well as DNA tension sensor tec
224 experiments of membrane proteins aligned in lipid bilayers provide tilt and rotation angles for alph
226 uctures determined in detergent micelles and lipid bilayers related to reorganization of intersubunit
227 n nanotubes capable of self-inserting into a lipid bilayer, represent a simplified model of biologica
228 an be used to speed-up data acquisition from lipid bilayer samples and also to provide structural inf
229 cellular vesicles (EVs) are membrane-derived lipid bilayers secreted by bacteria and eukaryotic cells
230 tic lateral membrane pressure profile in the lipid bilayer sensed by LHCII-bound peripheral pigments.
231 ivation and establish a new location for the lipid bilayer, shifted ~14 angstrom from previous consen
232 D) biosensor functionalized with a supported lipid bilayer (SLB) and MAG, we detect vesicular GD1a an
233 ental approaches, hybrid live cell-supported lipid bilayer (SLB) systems, wherein a live cell interac
234 e perform ITIR-FCS measurements on supported lipid bilayers (SLBs) of various lipid compositions to c
235 phosphatidylserine (PS) lipids in supported lipid bilayers (SLBs), forming a PS-Zn(2+) complex with
237 des in an environment made up largely by the lipid bilayer, so lipids play a central role on its stab
238 stance, in areas where spectrin binds to the lipid bilayer, spectrin filaments would restrict diffusi
239 E) material, named S6, is designed to have a lipid-bilayer stabilizing topology afforded by an extend
240 upt ER membrane homeostasis, we identified a lipid bilayer stress (LBS) sensor in the UPR transducer
241 ies effect originates from a looser swelling lipid bilayer structure due to the adsorption and electr
243 We used microtubule gliding assays on a lipid bilayer substrate to investigate the role of membr
246 learly indicate that the presence of MGDG in lipid bilayers switches LHCII from a light-harvesting to
248 cardiolipin-dependent properties of ternary lipid bilayer systems that mimic the major components of
250 eptor SpA was attached to BioPE-DOTAP binary lipid bilayer tethered on alkane thiol molecular cushion
251 ) of Gram-negative bacteria is an asymmetric lipid bilayer that consists of inner leaflet phospholipi
252 nuous lipid cubic phases consist of a single lipid bilayer that forms a continuous periodic membrane
253 ristics of transient pores on a patch of the lipid bilayer that is strengthened by an elastic meshwor
254 ible and hysteretic geometrical changes in a lipid bilayer that mimics the composition and structure
255 gical cells are enveloped by a heterogeneous lipid bilayer that prevents the uncontrolled exchange of
256 to build intact AE1 structures in a complex lipid bilayer that resembles the native erythrocyte plas
257 Finally, the attachment of GO to a supported lipid bilayer that was composed of zwitterionic 1,2-diol
258 of T cells interacting with glass-supported lipid bilayers that favor imaging but are orders of magn
260 ing the conduction domain construct of M2 in lipid bilayers, that the imidazole rings are hydrogen bo
261 d the structural topology of the MPER on the lipid bilayer, the adjacent transmembrane domain (TMD) w
262 pHLIP ICG interaction with the cell membrane lipid bilayer, the pharmacology and toxicology in vitro
264 Together with a finite element model of lipid bilayers, the reproduced responses suggest that th
266 zes a trimeric fusion (F) protein within its lipid bilayer to mediate membrane merger with a cell mem
267 t-harvesting complex II (LHCII) in thylakoid lipid bilayers to detect LHCII conformational dynamics i
270 simulate DPPC:DOPC and DPPC:DOPC:cholesterol lipid bilayers to investigate phase transitions at tempe
273 n the pathways of peptide insertion into the lipid bilayer (triggered by a pH drop) and peptide exit
274 f giant unilamellar vesicles and a supported lipid bilayer, triggered by calcium, promotes the lipid
276 l membrane proteins embedded in their native lipid bilayer, typically by retracting the cantilever at
277 ing between Anthracyclines and two different lipid bilayers (unsaturated POPC and saturated DMPC) is
278 eptide-cholesterol contacts in virus-mimetic lipid bilayers using solid-state NMR spectroscopy, and a
279 rus embedded in synthetic liquid crystalline lipid bilayers using two-dimensional J-resolved NMR spec
281 mpositionally well-defined large unilamellar lipid bilayer vesicles to study the impact of MGDG on li
282 ab' ligand that, when coupled to a supported lipid bilayer via DNA complementation, triggers TCRs and
283 The results indicate that Lti30 binds the lipid bilayer via electrostatics, which restricts the mo
284 (3D) lattice of P2 molecules between stacked lipid bilayers, visualizing supramolecular assembly at t
286 th adhesion proteins anchored to a supported lipid bilayer, we find that probes are excluded from con
287 folding status of reconstituted hairpins in lipid bilayers, we found that the E217G hairpin exhibits
288 attachment dynamics of motors bound to fluid lipid bilayers, we quantified the microtubule accumulati
290 extracellular domains tethered to supported lipid bilayers, were studied using a combination of dyna
291 ak alpha-helical geometry halfway across the lipid bilayer where ion binding sites are organized arou
292 ealed that the TMD is well-inserted into the lipid bilayer, whereas the FPPR and MPER are exposed to
293 OXPHOS system imposes packing stress on the lipid bilayer, which is relieved by CL remodeling to for
294 to each other by spectrin tetramers, and the lipid bilayer, which is tethered to the skeleton via, at
295 icles then spontaneously fused with a planar lipid bilayer, which produced stepwise increases of ion
299 peptide disc mediated formation of supported lipid bilayers with membrane proteins represents an attr
300 essful incorporation of membrane proteins in lipid bilayers with sufficiently high concentration and