ライフサイエンスコーパス: natural peptide

1 anced antibacterial activity relative to the natural peptide.

2 ional space that could not be reached by the natural peptide.

3 to one of the mimotope peptides than to the natural peptide.

4 nd demonstrate a 3-fold enhancement over the natural peptide.

5 e, alpha(v)beta5, as effectively as does the natural peptide.

6 kbone oligomers ("foldamers") that fold like natural peptides.

7 robial properties of certain natural and non-natural peptides.

8 CD4 T cells that recognized three different natural peptides.

9 liquid chromatography of both synthetic and natural peptides.

10 ve recently been explored as mimics of these natural peptides.

11 all protein-like molecules designed to mimic natural peptides.

12 play procedure provides a generic way to non-natural peptide adhesion domains, which not only mimic n

13 AT(1) receptors and similar affinity for the natural peptide agonist angiotensin II.

14 oupled receptors is critically important for natural peptide agonist binding and action.

15 Natural peptide agonists of corticotrophin-releasing fac

16 Non-natural peptide analogs have significant potential for t

17 odified decamer is more immunogenic than the natural peptide and a candidate for peptide-based melano

18 owed that it had no effect on the binding of natural peptide and nonpeptidyl ligands of this receptor

19 structural elements, as the backbones of all natural peptides and proteins are composed of amide bond

20 The ability of natural peptides and proteins to influence the formation

21 Natural peptide antibiotics are part of host innate immu

22 Synthetic peptides modeled after natural peptide antibiotics interfere with microbial mem

23 whereby approximately 1.5 million novel and natural peptides are fabricated on the scaffold present

24 ules governing conformational preferences in natural peptides are poorly understood, and consequently

25 However, these natural peptides as well as their beta-peptide analogues

26 Synthetic and natural peptide assemblies can possess transport or cond

27 cent protein of Aequorea victoria (GFP) is a natural peptide chromophore without substrate or cofacto

28 is attributable to C-terminal amidation of a natural peptide derived from osteocalcin.

29 The natural peptides FMRFamide and FLRFamide only activated

30 The overall strategy of identifying natural peptides from islet beta-cells opens up new aven

31 oating luminescent gold nanoparticles with a natural peptide, glutathione, and the simplest stable am

32 These results suggest that the natural peptide histogranin may be a novel adjunct in ne

33 lly equal to or potentially more potent than natural peptides in stimulating CTL responses; therefore

34 RAP1/2), and N-terminally extended model and natural peptides in their free and HLA-B*0801-bound form

35 en extensively investigated in synthetic and natural peptides, including by nanosecond kinetic studie

36 compound, a 150-fold higher potency than the natural peptide inhibitor (IC50 2.9 muM).

37 lutamate-containing 27-residue peptide, is a natural peptide inhibitor of the N-methyl-d-aspartate (N

38 ural basis for the domain selectivity of the natural peptide inhibitors of ACE, bradykinin potentiati

39 tures of these segments, we designed two non-natural peptide inhibitors that block aggregation.

40 Epitope discovery from natural peptide libraries is a promising route to subuni

41 ontrast, 50% of the peptides selected from a natural peptide library, in which phage display segments

42 ghts into the conformation and dynamics of a natural peptide ligand docked to a Family B G protein-co

43 elucidate the structural basis of binding a natural peptide ligand to a family A G protein-coupled r

44 The recently identified natural peptide ligand, tuberoinfundibular peptide of 39

45 with the action mechanism of the receptor's natural peptide ligand.

46 evident that the carboxyl-terminal region of natural peptide ligands bind to the amino-terminal domai

47 Besides natural peptide ligands, screening of random peptide lib

48 TCR engagement with natural peptide-MHC class I agonist resulted in the same

49 natural polymers that mimic the functions of natural peptides or proteins in their ability to direct

50 pitope motif (QKRAA) was as effective as the natural peptide p135H sequence for inducing arthritis.

51 esults indicate that along with the abundant natural peptides p2Ca and p2Cb, the QL9 and other OGDH p

52 that the hydrolytic stability of functional, natural peptide sequences can be improved by two orders

53 Natural peptide sequences ligate to dirhodium centers th

54 When JG-365 was converted into the natural peptide substrate for molecular dynamic simulati

55 We have identified the natural peptide target of a CTL clone that recognizes th

56 Synthetic and natural peptides that act as nonselective melanocortin r

57 Due to the limited availability of natural peptides, the properties of human epithelial def

58 The conformation of the natural peptide [Thr6]-bradykinin, Arg1-Pro2-Pro3-Gly4-P

59 The natural peptide [Thr6]-bradykinin, Arg1-Pro2-Pro3-Gly4-P

60 Analysis of the disulfide bridges of a natural peptide tx3c from C. textile and synthetic pepti

61 The fragmentation of natural peptides using dynamic collision-induced dissoci

62 against multiple citrullinated synthetic and natural peptides was recently developed and used to stai

63 ne somatostatin, a pharmaceutically relevant natural peptide, which contains a Trp-based type II' bet

64 red mice were used to determine which of the natural peptides with natriuretic peptide-like structure

65 It is also proposed that natural peptides with the ability to promote biominerali

66 iple analysis steps to locate and quantitate natural peptides within a single experiment and to align

67 novel algorithms for detecting signatures of natural peptides within a single LC-MS measurement and c