ライフサイエンスコーパス: antifreeze protein

1 or the repetitive tripeptide backbone of the antifreeze protein.

2 mal hysteresis as a functional effect of the antifreeze proteins.

3 comparable to that of the most active insect antifreeze proteins.

4 ilar to that of freezing point depression by antifreeze proteins.

5 Such repeats are a common feature of animal antifreeze proteins.

6 ch is known as an enhancer of certain insect antifreeze proteins.

7 synthetic macromolecular (polymer) mimics of antifreeze proteins.

8 lvent interaction of an ice-binding type III antifreeze protein (AFP III) and ubiquitin a non-ice-bin

9 We have studied the winter flounder antifreeze protein (AFP) and two of its mutants using mo

10 The TH activity of an antifreeze protein (AFP) depends on the specific AFP and

11 stereospecific binding of shorthorn sculpin antifreeze protein (AFP) to (2 -1 0) secondary prism fac

12 An antifreeze protein (AFP) with no known homologs has been

13 enes encoding insect, Dendroides canadensis, antifreeze proteins (AFP) were produced by Agrobacterium

14 Since antifreeze proteins (AFPs) act as KHIs, we have used the

15 Antifreeze proteins (AFPs) and antifreeze glycoproteins

16 Antifreeze proteins (AFPs) are a subset of ice-binding p

17 Antifreeze proteins (AFPs) are a unique class of protein

18 The primary sequences of type I antifreeze proteins (AFPs) are Ala rich and contain thre

19 Antifreeze proteins (AFPs) are found in fish, insects, p

20 Antifreeze proteins (AFPs) are of great importance for a

21 Type III antifreeze proteins (AFPs) are present in the body fluid

22 Antifreeze proteins (AFPs) are specific proteins that ar

23 The antifreeze proteins (AFPs) bind ice nuclei and depress t

24 Antifreeze proteins (AFPs) can produce a difference betw

25 Antifreeze proteins (AFPs) have been identified in certa

26 Antifreeze proteins (AFPs) have independently evolved in

27 Antifreeze proteins (AFPs) help some organisms resist fr

28 Antifreeze proteins (AFPs) make up a class of structural

29 Antifreeze proteins (AFPs) of polar marine teleost fishe

30 subpolar marine teleost fishes have evolved antifreeze proteins (AFPs) or antifreeze glycoproteins (

31 Antifreeze proteins (AFPs) protect certain cold-adapted

32 Antifreeze proteins (AFPs) protect certain organisms fro

33 Antifreeze proteins (AFPs) protect many plants and organ

34 It has been argued that for antifreeze proteins (AFPs) to stop ice crystal growth, t

35 Antifreeze proteins (AFPs), known to protect organisms f

36 basis of the cytoprotective capabilities of antifreeze proteins (AFPs), we hypothesized that supplem

37 om freezing by the presence of extracellular antifreeze proteins (AFPs), which bind to ice, modify it

38 limit supercooling and induce freezing, and antifreeze proteins (AFPs), which function to prevent fr

39 dy plants, and overwintering insects produce antifreeze proteins (AFPs), which lower the freezing poi

40 It appears that antifreeze proteins and antifreeze glycoproteins have re

41 both have been implicated in the activity of antifreeze proteins and antifreeze glycoproteins.

42 f hydrogen bond dynamics for the function of antifreeze proteins and for molecular recognition.

43 Antifreeze proteins and glycoproteins [AF(G)Ps] have bee

44 que polysaccharide resemble those present in antifreeze proteins and glycoproteins.

45 Type III antifreeze proteins are found in Arctic and Antarctic ee

46 vation of donor cells and tissue, but native antifreeze proteins are often not suitable, nor easily a

47 Antifreeze proteins are produced by extremophile species

48 For instance, antifreeze proteins, bovine serum albumin, and ovomucoid

49 ers which have no structural similarities to antifreeze proteins but reproduce the same macroscopic p

50 Thus, the antifreeze protein can bind to the molecularly rough ice

51 s (antifreeze activity) produced by purified antifreeze proteins (DAFPs) from the larvae of the beetl

52 Dendroides canadensis produce a family of 13 antifreeze proteins (DAFPs), four of which are in the he

53 fibrils formed from engineered R. inquisitor antifreeze protein, depending upon geometry, we estimate

54 tures (spruce budworm and Rhagium inquisitor antifreeze proteins) derived from sonication-based measu

55 We hypothesize that antifreeze protein diversity is an important contributor

56 dentification of a phenotype associated with antifreeze protein expression in plant tissue.

57 ave used site-selective strategies to attach antifreeze proteins found in Arctic fish and insects to

58 ed to investigate the mechanism by which the antifreeze protein from the spruce budworm, Choristoneur

59 Antifreeze proteins from polar fish species are remarkab

60 A synthetic antifreeze protein gene was expressed in plants and redu

61 The antifreeze protein genes, both with and without the sign

62 e of large-molecular-mass antifreezes (e.g., antifreeze proteins), has been described in animals, pla

63 olecular evolution and diversity of Type III antifreeze proteins in a single individual Antarctic fis

64 ng avoidance conferred by different types of antifreeze proteins in various polar and subpolar fishes

65 Although structurally diverse, all antifreeze proteins interact with ice surfaces, depress

66 ng that increased activity of the two-domain antifreeze protein is not dependent on structure of the

67 The sequence of carrot antifreeze protein is similar to that of polygalacturona

68 yoprotection by a dehydrin is not due to any antifreeze protein-like activity, as has been reported p

69 Antifreeze proteins lower the noncolligative freezing po

70 This opens up a new field of metallo-organic antifreeze protein mimetics and provides insight into th

71 carrot shares these functional features with antifreeze proteins of fish.

72 Antifreeze proteins prevent ice crystal growth in extrac

73 rimary sequence of the mature spruce budworm antifreeze protein (sbwAFP) was constructed by primer ov

74 e recently discovered glycine-rich snow flea antifreeze protein (sfAFP) has no sequence homology with

75 Here, we show that, for the snow flea antifreeze protein (sfAFP), stability and cooperativity

76 termine the X-ray structure of the snow flea antifreeze protein (sfAFP).

77 initiate the crystallization process of the antifreeze protein solution.

78 The gene for a thermal hysteresis (antifreeze) protein (sthp-64) from the bittersweet night

79 s C, in part by synthesizing the most potent antifreeze protein studied thus far (RiAFP).

80 ure of RD3, a naturally occurring two-domain antifreeze protein, suggests that the two nearly identic

81 pted to live at subzero temperatures express antifreeze proteins that improve their tolerance to free

82 proline as a minimum (bio)synthetic mimic of antifreeze proteins that is accessible by solution, soli

83 ore, we identify three properties of Type I "antifreeze" proteins that discriminate among these two o

84 n the initial recognition and binding of the antifreeze protein to ice by lowering the barrier for bi

85 Ice-binding proteins (IBPs), also known as antifreeze proteins, were added to ice cream to investig

86 the properties of water at the surface of an antifreeze protein with femtosecond surface sum frequenc