ライフサイエンスコーパス: artificial membrane

1 the binding and kinetics of Arf and Brag2 in artificial membranes.

2 lipid mixing between distinct populations of artificial membranes.

3 is significantly lower in biological than in artificial membranes.

4 ed highly homogeneous channels when added to artificial membranes.

5 mediate effective fusion of both native and artificial membranes.

6 etergent micelles, and when reconstituted in artificial membranes.

7 n detergent micelles compared with native or artificial membranes.

8 P radically alters how it interacts with the artificial membranes.

9 tic GPCR, into both lipid- and polymer-based artificial membranes.

10 functional significance of this FP by using artificial membranes.

11 lar processes and important to the design of artificial membranes.

12 e toxin pores in both human erythrocytes and artificial membranes.

13 two or three dimensions into non-lipid-based artificial membranes.

14 mucin mimetics and their incorporation into artificial membranes.

15 from the spontaneity of the interaction with artificial membranes.

16 of PC2 forms an alpha-helix and inserts into artificial membranes.

17 -2, and BAX can form ion-conductive pores in artificial membranes.

18 Gangliosides embedded within an artificial membrane also bind to the RBD.

19 aphorase functions as an antioxidant in both artificial membrane and natural membrane systems by acti

20 urotoxicity (measured by permeabilization of artificial membranes and by loss of neurons in primary n

21 Permeability through artificial membranes and Caco-2 cell monolayers in vitro

22 plementation of such biological functions in artificial membranes and demonstrate two-dimensional sel

23 Experiments using artificial membranes and filamentous cells suggest that

24 a, demonstrating their effectiveness in both artificial membranes and live cells.

25 -step model applies to biological as well as artificial membranes and that a limiting step in the hyd

26 applications, such as in molecular sensors, artificial membranes, and as catalysts.

27 lipids, opening ion conductance pathways in artificial membranes, and integrating into natural membr

28 ith CPE, but not with sphingomyelin-enriched artificial membranes, and that RahU interacts with the i

29 eral principles identified from studies with artificial membranes apply to biological systems.

30 Experiments on artificial membranes are revealing many details about th

31 rnary lipid mixture, we demonstrate that the artificial membrane-associated cytoskeleton, on the one

32 crometer-sized rafts are readily observed in artificial membranes, attempts to observe analogous doma

33 p7 and myristoylated p15 fragments of BID to artificial membranes bearing the lipid composition of mi

34 aAPC are based on artificial membrane bilayers containing discrete membran

35 mbrane interaction than the charge-dependent artificial membrane binding, and the mode of interaction

36 Herein, we design a novel modular artificial membrane-binding protein (AMBP) platform for

37 Artificial membrane-bound vesicles, known as liposomes,

38 Most often membrane proteins are studied in artificial membranes, but such artificial systems do not

39 c issues, we assessed the binding of StAR to artificial membranes by fluorescence resonance energy tr

40 is an important phenomenon in biological and artificial membranes, channels, and nanopores.

41 tion capacity factor (k(IAM)) on immobilized artificial membrane chromatography columns (IAM-HPLC) is

42 atographic measurements using an immobilized artificial membrane column provide the most precise esti

43 The dynamics of water at the surface of artificial membranes composed of aligned multibilayers o

44 Quantitative kinetic studies using artificial membranes confirm that receptor dimerization

45 e have mimicked this interaction by using an artificial membrane containing synthetic Galcer and reco

46 This peptide binds and disrupts artificial membranes containing lipids typically enriche

47 In vitro, synuclein fragments artificial membranes containing the mitochondrial lipid

48 ere we report on the design and synthesis of artificial membranes embedded with synthetic, self-repro

49 bic substrates in a detergent-free native or artificial membrane environment.

50 boid proteins in both detergent micelles and artificial membrane environments.

51 e also failed to promote blood feeding on an artificial membrane feeder.

52 Artificial membrane feeding (AMF) is a powerful and vers

53 An artificial membrane feeding system containing a high tit

54 acquisition and transmission we developed an artificial membrane feeding system for O. hermsi nymphs

55 n of LSDV by Ae. aegypti after feeding on an artificial membrane feeding system that contained a high

56 is study was to adapt a previously developed artificial membrane feeding system to complete the life

57 and retention of LSDV by Ae. aegypti from an artificial membrane feeding system was also examined.

58 d from P. vivax-infected patients through an artificial membrane-feeding system, which in turns requi

59 es and feeding them to mosquitoes through an artificial membrane followed by assessment of infection

60 iquid-liquid phase separation in natural and artificial membranes, fundamental questions have persist

61 ro assays, particularly reconstitution using artificial membranes, have established the role of synap

62 ion in living systems or reconstitution into artificial membranes; however these approaches have inhe

63 data and an in vitro parameter, immobilized artificial membrane (IAM) chromatography was performed.

64 nts, as determined by HPLC on an immobilized artificial membrane (IAM) column, and serum rhGH concent

65 5R, have been immobilized on the immobilized artificial membrane (IAM) liquid chromatographic station

66 the phospholipid monolayer of an immobilized artificial membrane (IAM) liquid chromatography (LC) sta

67 omimetic chromatography utilizes immobilized artificial membrane (IAM), human serum albumin (HSA), an

68 a chromatographic tool based on immobilized artificial membranes (IAM-HPLC) and with quantum-chemist

69 zes to the nerve terminal and interacts with artificial membranes in vitro but binds weakly to native

70 out capsids when expressed ectopically or on artificial membranes in vitro, but not in the infected c

71 ssential for the fusion of alphaviruses with artificial membranes (liposomes).

72 tor (beta(2)-AR) have been immobilized on an artificial membrane liquid chromatographic stationary ph

73 holipid analogue monolayer of an immobilized artificial membrane liquid chromatographic stationary ph

74 ention coefficients, measured by immobilized artificial membrane liquid chromatography (IAM-LC) and b

75 Artificial membranes may be resistant or susceptible to

76 We thus report an artificial membrane metalloprotein with the potential to

77 the blood-brain barrier, as predicted in an artificial membrane model assay and demonstrated in ex v

78 bolic network can drive dynamic behaviour in artificial membranes, offering insights into mechanisms

79 en major brain gangliosides were adsorbed as artificial membranes on plastic microwells, only GT1b an

80 clamp uses computer simulation to introduce artificial membrane or synaptic conductances into biolog

81 s amphiphilic self-assembled systems such as artificial membranes or cell walls.

82 tudies are normally obtained in vitro and in artificial membranes or detergent.

83 s paves the way for practical application of artificial membranes or droplet networks in diverse area

84 pparent permeability values in both parallel artificial membrane permeability assay (PAMPA) and blood

85 r permeability was then assessed in parallel artificial membrane permeability assay (PAMPA) and Caco-

86 permeability was assessed using the parallel artificial membrane permeability assay (PAMPA) and Caco-

87 ere obtained experimentally using a parallel artificial membrane permeability assay (PAMPA) and showe

88 ological pH) were studied using the parallel artificial membrane permeability assay (PAMPA) at pH 6.5

89 macrocycles was evaluated through a parallel artificial membrane permeability assay (PAMPA), and the

90 transwell assay and the noncellular parallel artificial membrane permeability assay (PAMPA).

91 ouse NP constituent library via the Parallel Artificial Membrane Permeability Assay (PAMPA-BBB), with

92 mbrane permeability was assessed by parallel artificial membrane permeability assay and Caco-2 assay.

93 16 (PhPro)4 stereoisomers using the parallel artificial membrane permeability assay and looked at dif

94 ological polar surface area and the parallel artificial membrane permeability assay for rank-ordering

95 ilico model as well as a customized parallel artificial membrane permeability assay indicated good sk

96 ention measurements determined by a parallel artificial membrane permeability assay was drawn.

97 BBB permeability was assessed by parallel artificial membrane permeability assays and P-glycoprote

98 ate to high passive permeability in parallel artificial membrane permeability assays.

99 nhibition activities, anti-fIIa activity and artificial membrane permeability were considerably impro

100 ed liquid membrane, is based on the parallel artificial membrane permeation assay (PAMPA), widely use

101 he blood-brain barrier according to parallel artificial membrane permeation assay.

102 Data sets for the artificial membrane permeation rate and for clearance in

103 by immobilization on either the immobilized artificial membrane-phosphatidyl choline (IAM-PC) statio

104 oparticle encapsulation, the construction of artificial membrane pores and as structural scaffolds th

105 ntary membrane proteins, and that orthogonal artificial membrane proteins can influence the cofactor

106 approach to readily-expressible, versatile, artificial membrane proteins for more accessible study a

107 Artificial membrane receptors (R)-1 and (S)-1 are helica

108 However, using artificial membranes requires challenging protein purifi

109 ly, addition of the cytosolic preparation to artificial membranes resulted in the transient, charge-i

110 the recombinant, non-lipidated protein into artificial membranes results in bilayer destabilization

111 ll out within 12 h, induction continued with artificial membrane rupture and oxytocin, administered t

112 Neutron reflection measurements on artificial membranes, so-called sparsely tethered bilaye

113 s expressing the subtypes and an immobilized artificial membrane stationary phase.

114 mbrane binding, which is concordant with the artificial membrane studies.

115 anopores known as hybrid nanopores, where an artificial membrane substitutes the organic support memb

116 soforms respond differently to properties of artificial membranes such as surface charge, they should

117 subunits was analyzed by crosslinking to an artificial membrane surface and by electron microscopy o

118 nar lipid bilayers are still the best-suited artificial membrane system for the study of reconstitute

119 An artificial membrane system was optimized for application

120 a protein anchor and reconstituted inside an artificial membrane system.

121 and compared in rat liver microsomes and an artificial membrane system.

122 Artificial membrane systems allow researchers to study t

123 eins have been successfully reconstituted in artificial membrane systems for sensing purposes.

124 target proteins into proteoliposomes (PLs), artificial membrane systems of defined lipid composition

125 Artificial membrane tethering of centralspindlin restore

126 Artificial membrane tethering of Ste5(R407S K411S) resto

127 Artificial membrane tethering of the PTEN mutants effect

128 ant efforts have been devoted to fabricating artificial membranes that can mimic the delicate functio

129 BAX and BCL-2 each form channels in artificial membranes that have distinct characteristics

130 ater dynamics may guide the future design of artificial membranes that rapidly transport protons and

131 However, contrary to the interaction with artificial membranes, the interaction with biological me

132 have shown that cholesterol may nucleate in artificial membranes to form thick two-dimensional bilay

133 he transferability of conclusions drawn from artificial membranes to live cells.

134 re have been tremendous advances in creating artificial membranes to model the properties of native m

135 SNARE proteins are sufficient to fuse artificial membranes together.

136 approach to achieve voltage-switchability in artificial membrane transport systems.

137 Lipid mixtures within artificial membranes undergo a separation into liquid-di

138 Herein the influence of limonene on artificial membranes was studied to verify the effect of

139 s disease forms calcium permeant channels in artificial membranes, we have proposed that the intracel

140 found that alpha-synuclein binds directly to artificial membranes whose lipid composition mimics that

141 Irradiation of this artificial membrane with visible light results in the un

142 lpha-synuclein binds with higher affinity to artificial membranes with the PS head group on the polyu