ライフサイエンスコーパス: pleated

1 olves within 3-5 days, the mesh is gradually pleated, allowing delayed fascial closure); stage II, ab

2 New pleated and coiled geometries for the compact layout of

3 conformers, including ribbonlike structures pleated around a rarely observed series of intramolecula

4 ficant deviation is that the chains met in a pleated arrangement at the bilayer center, although they

5 constructed an atomic model for the twisted pleated beta-sheet of human Abeta amyloid protofilament.

6 The architecture of two pleated beta-sheets and the conformation of the H1 and H

7 loid fibrils have suggested that the stacked pleated beta-sheets are twisted so that a repeating unit

8 hat the Abeta deposit assumes a compact beta-pleated conformation.

9 he sequence Dan-Ndi-Dan was shown to adopt a pleated fold in solution, while its constitutional isome

10 ami' method to producing 3D shapes formed as pleated layers of double helices constrained to a honeyc

11 ng custom three-dimensional shapes formed as pleated layers of helices constrained to a honeycomb lat

12 ed, three-dimensional (3D) objects formed as pleated layers of helices constrained to a honeycomb lat

13 n of aedamers--foldamers that adopt a novel, pleated secondary structure in aqueous solution.

14 D spectrum was consistent with a mostly beta-pleated secondary structure.

15 gn of DNA sequences for folding 3D honeycomb-pleated shapes A series of rectangular-block motifs were

16 und-B (PiB) binds with high affinity to beta-pleated sheet aggregates of the amyloid-beta (Abeta) pep

17 amyloid-beta or phosphorylated tau in a beta-pleated sheet amyloid configuration.

18 r more alpha-helices, a middle layer of beta-pleated sheet and a top layer formed by segments of the

19 ucture of this protein has considerable beta-pleated sheet and is very compact.

20 beta-hairpin conformation and extended beta-pleated sheet assembly have been characterized by single

21 ructure, must undergo a transition to a beta-pleated sheet by a mechanism shared by other lipoprotein

22 ties in vivo when it adopts a fibrillar beta-pleated sheet conformation.

23 t rather seemed to be directed toward a beta-pleated sheet conformational epitope expressed by AL and

24 e sites are thought to be important for beta-pleated sheet formation.

25 -beta-strand turn of the three-stranded beta-pleated sheet of beta2m.

26 The pleated sheet region of the leucine-rich G-protein-coupl

27 ve and below peptide planes of internal beta-pleated sheet residues in five globular proteins.

28 proteins, we observe the formation of alpha-pleated sheet secondary structure, which was first propo

29 that tear lipocalins have a predominant beta-pleated sheet structure (44%) that is essentially retain

30 ansthyretin and beta(2)-microglobulin, alpha-pleated sheet structure formed over the strands that are

31 We propose that the formation of alpha-pleated sheet structure may be a common conformational t

32 1-42) into the neurotoxic amyloid-like, beta-pleated sheet structure, and instead encourages folding

33 hosphorylated, and nor did they contain beta-pleated sheet structure.

34 dyes that bind specifically to crossed beta-pleated sheet structures (eg, Congo red, Thioflavin S).

35 that the trimers were formed mainly of beta-pleated sheet structures in detergent micelles.

36 its, the ABri peptide adopts aggregated beta-pleated sheet structures, similar to those formed by the

37 omain is characterized by 10 strands of beta-pleated sheet that form two distinct layers which lie ne

38 nsists of a single twisted antiparallel beta-pleated sheet with Greek-key topology.

39 sed of 27 +/- 3% alpha-helix, 20 +/- 3% beta-pleated sheet, and 53 +/- 3% coil.

40 In addition, the 2 beta-pleated sheet-derived peptides and the alpha1-derived pe

41 In particular, the 2 beta-pleated sheet-derived peptides covering residues 91 to 1

42 eight-stranded cup-shaped anti-parallel beta-pleated sheet.

43 are predicted to have a high content of beta-pleated sheet.

44 structural element of the antiparallel beta-pleated sheet.

45 formations into soluble, macromolecular beta-pleated-sheet complexes without any covalent modificatio

46 Significance for controlling beta-pleated-sheet content during thermal processing of bioma

47 Beta-pleated-sheet crystals are among the most stable of prot

48 ng, and the accepted paradigm, was that beta-pleated-sheet crystals in the dry solid state were so st

49 llar crystals of synthetic polymers and beta-pleated-sheet crystals is confirmed.

50 rn that assumption and demonstrate that beta-pleated-sheet crystals melt directly from the solid stat

51 t reversible thermal melting of protein beta-pleated-sheet crystals, exemplified by silk fibroin.

52 rmation into insoluble cell-deleterious beta-pleated-sheet motifs.

53 s are discussed, namely tight (occludin) and pleated-sheet septate (neurexin IV).

54 forms in the peripheral nervous system where pleated-sheet septate junctions bond cells of the nascen

55 structural analogs of the BBB are occlusive (pleated-sheet) septate and tight junctions between perin

56 ) polymers that self-assemble into nanoscale pleated sheets of hairpin RNA, which in turn form sponge

57 support the changing of the alpha-helix/beta-pleated sheets ratio in protein structure analysis.

58 ere we show that this gB fragment forms beta-pleated sheets, self-assembles into fibrils that are thi

59 osed of two three-stranded antiparallel beta-pleated sheets.

60 peptide (Abeta), which forms fibrils of beta-pleated sheets.

61 oximately perpendicular to the faces of beta-pleated sheets.

62 aracteristics consistent with folding in the pleated, stacked geometry characteristic of this class o

63 Cultures in collagen-coated pleated surface roller bottles, with hepatocyte growth m

64 ting model, where each fibrillin molecule is pleated within one microfibril period allowing extensibi