ライフサイエンスコーパス: biomembrane

1 t on direct interactions between ILs and the biomembrane.

2 nel architecture for active transport across biomembranes.

3 lipids in curved regions and vesicle buds of biomembranes.

4 nderstanding of lateral heterogeneity within biomembranes.

5 ets to test the effect of immunoglobulins on biomembranes.

6 n approach used during domain isolation from biomembranes.

7 ically well-defined lipid bilayer models for biomembranes.

8 hydrophilic proteins can bind transiently to biomembranes.

9 idylcholine were used in this study to mimic biomembranes.

10 rameter to monitor packaging and fluidity of biomembranes.

11 to muscle components like myofibrils and/or biomembranes.

12 ol transport of these charged species across biomembranes.

13 sion of the freezing point of transitions in biomembranes.

14 t can aid in the characterization of complex biomembranes.

15 ow that TX-100 has a restructuring action on biomembranes.

16 otein association and protein insertion into biomembranes.

17 the asymmetric distribution of components in biomembranes.

18 duce targeted binding of amyloid deposits to biomembranes.

19 the importance of the collective dynamics of biomembranes.

20 omplex, stable, and impermeable phospholipid biomembranes.

21 -55,940 partitions with high efficiency into biomembranes.

22 f bubbles in foams, and pattern formation in biomembranes.

23 haracterization of composition variations in biomembranes.

24 lipids can induce dramatic shape changes in biomembranes.

25 triggering a dramatic change in the shape of biomembranes.

26 efficient to deplete cholesterol (Chol) from biomembranes.

27 tudies on mass transport characterization of biomembranes.

28 nd stability of pores formed in vesicles and biomembranes.

29 teins in stabilizing nascent fusion pores in biomembranes; a function inferred from recent experiment

30 tly taking into account the mechanics of the biomembrane and cytoskeleton.

31 pyridine) were prepared as model systems for biomembranes and cells and studied by scanning electroch

32 redict passive permeation of peptides across biomembranes and for determining the thermodynamics of p

33 Omega-3 and -6 PUFAs are key components of biomembranes and play important roles in cell integrity,

34 demonstrate an affinity of superwarfarins to biomembranes and suggest that cellular responses to thes

35 Molecular self-assembly, the function of biomembranes and the performance of organic solar cells

36 across the bilayer indicated that asymmetric biomembranes are assembled and maintained by specific me

37 Biomembranes are thin capacitors with the unique feature

38 nine, a dye that is commonly used in various biomembrane assays.

39 e catalysis demands the generation of intact biomembrane assemblies with structural integrity and lat

40 beta-sheet aggregates upon interacting with biomembranes at the onset of diseases, such as Parkinson

41 issue within a biomembrane requires that the biomembrane be biologically inert, and that the mean por

42 ng dynamic and topological information about biomembranes because the molecular interactions taking p

43 GTP-loaded K-Ras4B with heterogeneous model biomembranes by using a combination of different spectro

44 ing the molecular evolution of ion-selective biomembrane channels/transporters, globular proteins, an

45 Lipid bilayers are biomembranes common to cellular life and constitute a co

46 urface pressures (> or = 30 mN/m) that mimic biomembrane conditions.

47 ncluding those (pi > or =30 mN/m) that mimic biomembrane conditions.

48 cked using an activity-based probe, with the biomembranes delineated by carbocyanine lipid reporters.

49 apparently new possibilities in the study of biomembrane electrostatics and other bioelectric phenome

50 ay be correlated with the lipid diversity of biomembranes, for example, with regard to membrane curva

51 novel single-cell based nanotool termed dual biomembrane force probe (dBFP).

52 Using a biomembrane force probe capable of measuring single bond

53 Adhesion frequency experiments with a biomembrane force probe could not detect interactions of

54 We have used a biomembrane force probe decorated with P-selectin to for

55 ve dynamics simulations, we demonstrate that biomembrane force probe measurements of various P- and L

56 robes (e.g., the atomic force microscope and biomembrane force probe), P-selectin:PSGL-1 adhesion bon

57 Using a biomembrane force probe, we observed biphasic force-dece

58 Using a biomembrane force probe, we observed real-time reversibl

59 Using a flow chamber and biomembrane force probe, we show a triphasic force depen

60 al fluctuation and force-clamp assays with a biomembrane force probe.

61 tly larger than previously published for the biomembrane force probe.

62 ease/resumption in thermal fluctuations of a biomembrane force probe.

63 Using the biomembrane force-probe, the bond system was exposed to

64 nd is highly enriched in detergent-resistant biomembrane fractions associated with microdomains, i.e.

65 rate model shows that for proteins to drive biomembrane fusion at observed rates, they have to perfo

66 ative predictions about how proteins mediate biomembrane fusion.

67 oaded K-Ras4B with neutral and anionic model biomembranes has been investigated by a combination of d

68 roviding new insight into dynamic changes in biomembranes; however, few reports in the literature hav

69 termine whether a structurally heterogeneous biomembrane, human stratum corneum (SC), behaved as a ho

70 Biomembrane interfaces create regions of slowed water dy

71 Integrity of animal biomembranes is critical to preserve normal cellular fun

72 o probing for lipid phase domains in natural biomembranes is discussed.

73 The results show that PLA2 binding to model biomembranes is not significantly affected by pressure a

74 er study, the lipid composition of fusogenic biomembranes is quite complex.

75 eptides could increase the susceptibility of biomembrane lipids to fusion through an effect on lipid

76 understanding of how lipids and proteins in biomembranes may be obstructed by very small obstacles c

77 namics of small vesicles, diffusing close to biomembranes, may be spatially restricted by altering lo

78 These results show a new method to probe biomembrane mechanical properties using light as well as

79 and linear elasticity theories combined with biomembrane mechanics.

80 though lipid-dependent protein clustering in biomembranes mediates numerous functions, there is littl

81 , activity, and inhibition in a controllable biomembrane microenvironment.

82 yer, describes the conformation of TM-A in a biomembrane mimic, presents a peptide-bilayer model usef

83 0/C10-EPC remained lamellar in mixtures with biomembrane-mimicking lipid formulations [e.g., dioleoyl

84 The new biomembrane model challenges the standard model (the flu

85 giant unilamellar vesicles (GUVs, used as a biomembrane model) made by electroformation with varying

86 The assay applies to biomembrane models as well.

87 vide a basis for the construction of complex biomembrane models, which exhibit fluidity barriers and

88 opy has impeded distinction between numerous biomembrane models.

89 rotein function in a mixture as complex as a biomembrane, one must know whether the lipid composition

90 oxygen species that may damage organisms by biomembrane oxidation or mediate environmental transform

91 River humic acid (SRHA) causes an increased biomembrane perturbation (percent leakage of the fluores

92 The temperature studies revealed that biomembrane perturbation increases with decreasing tempe

93 nolamines (PEs), which are a common class of biomembrane phospholipids, typically display direct L(al

94 t the development of a microsphere supported-biomembrane platform enabling characterization of gamma-

95 Cu(+), Ag(+), Zn(2+), Cd(2+), Co(2+)) across biomembranes, playing a key role in homeostasis and in t

96 has been shown to mimic the protein-mediated biomembrane process.

97 of allogeneic or xenogeneic tissue within a biomembrane requires that the biomembrane be biologicall

98 eltaM2 segments were shown to oligomerize in biomembranes resulting in ion-channel activity with char

99 Overall, the notion that in biomembranes selected lipids could laterally aggregate t

100 Biomembranes serve barrier functions and serve as a stor

101 The mechanisms that mediate biomembrane shape transformations are of considerable in

102 We propose that by modeling these observed biomembrane shapes as fluid lipid bilayers in mechanical

103 yers as well as potential caveats in current biomembrane simulation methodology, including force-fiel

104 surface pressures (>30 mN/m) that mimic the biomembrane situation.

105 Phospholipid self-assembly is the basis of biomembrane stability.

106 e thermodynamic effects of anionic lipids on biomembrane stability.

107 ase as well as effects on biomacromolecules, biomembranes, subcellular structures and cells are discu

108 n the transmembrane region of SERCA near the biomembrane surface and interfere with calcium transport

109 (POPC) large unilamellar vesicle (LUV) model biomembrane system was studied by fluorescence spectrosc

110 possible to obtain structural parameters for biomembrane systems where isotope labeling may be prohib

111 affect the fusion rate in model membrane and biomembrane systems.

112 e a guideline for understanding more complex biomembrane systems.

113 In the environment of a typical biomembrane, the higher proportion of saturated fatty ac

114 ess transport or conductance activity across biomembranes through the formation of nanopores.

115 odetermines the complex lipid composition of biomembranes through tuning of kappa .

116 uence ranges from domain formation in intact biomembranes to membrane protein reconstitution and crys

117 the investigation of molecular processes at biomembranes using EW-CRDS for chemical species showing

118 tates in the absence and presence of a model biomembrane was probed by pressure perturbation.

119 The substrate loading into supported biomembranes was detergent-dependent, as evidenced by ev

120 mechanics can play in imaging multicomponent biomembranes with AFM.

121 s of active gamma-secretase within supported biomembranes with native-like fluidity.

122 The phenomenon of thermal fluctuation of a biomembrane within a stack of like membranes was introdu

123 and triggered its lipoplex to permeate model biomembranes within the time span of endosome processing