ライフサイエンスコーパス: bending rigidity

1 n membrane elasticity (area elastic modulus, bending rigidity).

2 affects global mechanical properties such as bending rigidity.

3 in polymerization and determine the filament bending rigidity.

4 the long-pitch helix and lowers the filament bending rigidity.

5 trans DOPC is suggestive of higher membrane bending rigidity.

6 of the spontaneous curvature and associated bending rigidity.

7 results also show that the gap has isotropic bending rigidity.

8 ments extend at low forces due to their high bending rigidity.

9 iciently high external forces due to its low bending rigidity.

10 in interactions alone contribute substantial bending rigidity (0.5 pN/nm) to ER/K alpha-helices.

11 r between the states depends on the membrane bending rigidity and charge density.

12 s the membranes' lateral compressibility and bending rigidity and demonstrates that the properties of

13 NA is confined at such high density that its bending rigidity and electrostatic self-repulsion presen

14 the molecule under tension, contour length, bending rigidity and intrinsic stiffness decreased in hy

15 lly controllable quantities such as membrane bending rigidity and receptor, coreceptor, and viral spi

16 een the physical properties of the membrane (bending rigidity and surface and dipole electrostatic po

17 the nanochannels is owing to an increase in bending rigidity and thickness of bottlebrush-coated DNA

18 We have developed a method to determine the bending rigidity and tilt modulus, for lipidic assemblie

19 ed by the membrane surface load and membrane bending rigidity, and changing information flow through

20 e's effects on lecithin membrane elasticity, bending rigidity, and strength.

21 ich the effective tissue properties, such as bending rigidity, are related explicitly to the paramete

22 al case, that spatial variations in membrane bending rigidity associated with lipid domains embedded

23 end this finding to SH3 domains a measure of bending rigidity based on loop curvature, which utilizes

24 We quantitatively measure the GO bending rigidity by characterizing the flattening of the

25 ns using temperature-invariant torsional and bending rigidities fail to predict the rather steep decl

26 Computations of bending rigidities for immunoglobulin-like domain protei

27 In these fragments the role of bending rigidity in determining the nature of the TSE ca

28 evealed increased elastic moduli and altered bending rigidity in vesicles incorporating HSAF.

29 properties, such as membrane undulations and bending rigidity, in a PIP2-dependent manner.

30 segments as entropic springs with different bending rigidities indicated that in the physiological S

31 rams of persistence length (measure of chain bending rigidity) indicated that the single molecule per

32 The calculated bending rigidity indicates weak microtubule doublet coup

33 c acids and flexible proteins, as far as its bending rigidity is concerned.

34 ed by its (central) DNA component, while its bending rigidity is controlled by its (eccentric) protei

35 e observation that GM1 decreased the bilayer bending rigidity is important for understanding the role

36 ven negative, and another where the membrane bending rigidity is lowered with a new class of helper-l

37 Heuristic estimates of the bilayer bending rigidity kappa and the area elastic modulus K(a)

38 The dynamic bending rigidity (kappa(d)), or equivalently the dynamic

39 layer thickness compressibility 1/B, bilayer bending rigidity Kc, the channel-bilayer mismatch Do, an

40 Following each bending rigidity measurement, a stretching (Young's) mod

41 For flat membranes, bending rigidities of approximately 100k(B)T, moderate e

42 We measured bending rigidities of B approximately 10(-22) N. m(2) fo

43 The bending rigidities of mitotic chromosomes isolated from

44 We further determined the bending rigidities of the coexisting domains and found t

45 rs is only 6x10(-27)Jm, much less than their bending rigidity of 5x10(-25)Jm.

46 Both the stretch modulus and the bending rigidity of a fiber change in the presence of va

47 Here, we used an optical trap to measure the bending rigidity of live Escherichia coli cells.

48 about two orders of magnitude lower than the bending rigidity of neat graphene.

49 bility can be smoothed out by increasing the bending rigidity of the coat, allowing for successful bu

50 The bending rigidity of the ER tubule membranes was found to

51 ration technique allowed measurements of the bending rigidity of the fluid phase only, whereas electr

52 A fragments: the equilibrium bend angle, the bending rigidity of the fragment axis, and the total twi

53 onformational heterogeneity decreases as the bending rigidity of the loop increases.

54 ropipette aspiration were used to assess the bending rigidity of the membrane as a function of GM1 co

55 ea compressibility modulus and, as such, the bending rigidity of the membrane is considerably reduced

56 we were able to control the diffusivity and bending rigidity of the membrane model.

57 th (Lp) of the molecule, indicating that the bending rigidity of the molecule was increased.

58 ermal energy becomes large compared with the bending rigidity of the shell.

59 We determined the bending rigidity of the single-stranded region in the ga

60 We determined the flexural (bending) rigidities of actin and cofilactin filaments fr

61 persistence length (a measure of the chain's bending rigidity) of 20 angstroms.

62 ein interaction, it is vital to know how DNA bending rigidity (or persistence length, a) depends on i

63 l-trap analyses are consistent with the high bending rigidity predicted by our model.

64 f tandem Ig and PEVK segments with different bending rigidities provides a unique passive force-SL re

65 emiquantitative predictions are made for the bending rigidity, radius, and axial tension of such brus

66 nd that the AT repeat has 28% (+/-12%) lower bending rigidity than a generic DNA sequence.

67 hich include the membrane charge density and bending rigidity, the membrane spontaneous curvature, th

68 Because DPPE and DPPC have different bending rigidities, these results establish that the pol

69 s and, from AFM measurements, estimate their bending rigidity to be 285 +/- 30 k(B)T, i.e., approxima

70 A similar bending rigidity was measured for newt chromosomes in vi

71 rol in the L(alpha) domains stabilizes their bending rigidity, which experiences a dramatic drop in t

72 crystalline structure, depending on the DNA bending rigidity, which is influenced by the ionic stren