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1 ntimicrobial peptides found in nature (e.g., magainins).
2  or neutral porphyrin, to a CAMP, buforin or magainin.
3  coli after conjugation to either buforin or magainin.
4 one to graded in the mutants of cecropin and magainin.
5 ic than other antimicrobial peptides such as magainin.
6                                       Unlike magainin 1 and cecropin P1, alpha-helical antimicrobial
7 he human defensin HNP-1 and the frog peptide magainin 1 elicited export of 17-kDa IL-1beta, but these
8 ement of birefringence during the binding of magainin 2 (Mag2) and a highly potent analogue in which
9                                              Magainin 2 (MAG2) and PGLa are two alpha-helical antimic
10                                     PGLa and magainin 2 (MAG2) are amphiphilic antimicrobial peptides
11 nergistic mechanism of equimolar mixtures of magainin 2 (MG2a) and PGLa in phosphatidylethanolamine/p
12  the two well-studied antimicrobial peptides magainin 2 (MG2a) and PGLa using lipid-only mimics of Gr
13                                              Magainin 2 (S8A, G13A, G18A) is a designed variant that
14                     The crystal structure of magainin 2 (S8A, G13A, G18A), obtained for the racemic f
15 f two prototypical linear cationic peptides: magainin 2 amide (which is selective for bacterial cells
16 ties than the natural antimicrobial peptides magainin 2 amide and cecropin B amide.
17                                        Ala19-magainin 2 amide exhibits both alpha-helix and beta-shee
18 xperiments indicate that alpha-helical Ala19-magainin 2 amide is bound near the phospholipid head gro
19 results obtained with two well-studied AMPs, magainin 2 and mastoparan X, and two model membranes ind
20 ance to protamine and alpha-helical peptides magainin 2 and melittin but not to beta-sheet defensin H
21 ecrete two exogenous antimicrobial peptides, magainin 2 and melittin.
22                                              Magainin 2 and PGLa are among the best-studied cationic
23                                   While both magainin 2 and pleurocidin are capable of disrupting bac
24  of which rendered Salmonella susceptible to magainin 2 and polymyxin B, but not defensin HNP-1.
25        The slyA mutant was hypersensitive to magainin 2 and polymyxin B, suggesting that the virulenc
26 for resistance to the antimicrobial peptides magainin 2 and polymyxin B.
27 play a role in the antibacterial activity of magainin 2 and related peptides.
28 hoP regulated and required for resistance to magainin 2 but not to polymyxin B or defensin HNP-1.
29 mate crystals that contain the d form of the magainin 2 derivative along with an l-peptide in which o
30 usly reported racemic crystal structure of a magainin 2 derivative displayed a homochiral antiparalle
31 e-active antibacterial peptide cecropin A or magainin 2 failed to inhibit the DnaK-mediated phosphate
32         Host-defense peptides (HDPs) such as magainin 2 have emerged as potential therapeutic agents
33  in-plane scattering detects pores formed by magainin 2 in membranes only when a substantial fraction
34 ary structure and location of an analogue of magainin 2 in synthetic phospholipid bilayers using a co
35                    We conclude that IAPP and magainin 2 induce membrane leakage and cytotoxicity thro
36  membranes by antimicrobial peptides such as magainin 2 is a significant activity performed by innate
37                                        Thus, magainin 2 is more sensitive to anionic lipid content th
38      The antiparallel dimer structure in the magainin 2 simulations resembles previously determined N
39              Remarkably, we observe IAPP and magainin 2 to be fully cross-cooperative in the inductio
40 nd insertion from solution of pleurocidin or magainin 2 to membranes representing the inner membrane
41 and helical tilt of an antimicrobial peptide magainin 2 using aligned X-band spin-label EPR spectrosc
42 anti-inflammatory effects of cecropin A(1-8)-magainin 2(1-12) hybrid peptide analog P5 on M. furfur.
43 ed for resistance to polymxyin B (but not to magainin 2) and is post-transcriptionally activated by t
44 tes the generation of natural peptides, like Magainin 2, and the derivatization of the protein Ubiqui
45                             D-Pyrrhocoricin, magainin 2, or buforin II, an antimicrobial peptide invo
46 onformational flexibility when compared with magainin 2, resists self-association at the membrane sur
47 crobial peptides including the alpha-helical magainin 2, the beta-sheet defensins and the cyclic lipo
48 tivity was found for the concerted action of magainin 2, the fungicidal lipopeptide class of surfacti
49 e antimicrobial peptide MSI-99, an analog of magainin 2, was expressed via the chloroplast genome to
50 e of the widely studied host-defense peptide magainin 2.
51 he sequences of delta-lysin, cecropin A, and magainin 2.
52 robial peptide cecropin A is tested here for magainin 2.
53          A cysteine substitution analogue of magainin-2 amide (magainin-F12W, N22C; denoted here as m
54 l peptides, MSI-78 and MSI-594, derived from magainin-2 and melittin, is presented.
55  membrane pores formed by the AMPs LL-37 and magainin-2.
56                                              Magainin, a 23-residue antibiotic peptide, interacts dir
57                                        Since magainin activity is modulated by oligomerization within
58 d that the helical peptides, alamethicin and magainin, also exhibit two distinct OCD basis spectra-on
59                                    Using the magainin analogue, pexiganan, as a model peptide we show
60 ries was essentially null, while fluorinated magainin analogues displayed an increase in hemolysis co
61 or oligomerization of specific highly active magainin analogues in membrane mimetic systems, we studi
62 ane-active antimicrobial peptides, including magainin and cecropin.
63 r to helical antimicrobial peptides, such as magainin and melittin.
64 istent with the two-state model exhibited by magainin and other small pore-forming peptides.
65 o two representative antimicrobial peptides, magainin and protegrin.
66  the toroidal pore model, first proposed for magainin and subsequently applied to PG-1.
67 t members of the alpha- and theta-defensins, magainins and cathelicidins had substantially higher lei
68 on of natural antimicrobial peptides such as magainins and cecropins.
69               Neutron diffraction shows that magainins and protegrins form stable pores in fully hydr
70                       alpha- and -defensin-, magainin-, and cathelicidin-type antimicrobial peptides
71  the diffraction patterns of alamethicin and magainin are similar to gramicidin except in the scale o
72                                              Magainins are antimicrobial peptides that selectively di
73                                              Magainins are cationic, membrane-active peptides which s
74 elittin pores are closely similar to that of magainin but unlike that of alamethicin.
75 anism, no peptide oligomerization occurs and magainin catalyzes dye release in proportion to its conc
76 nfiguration is consistent with all published magainin data.
77 ith antibiotic activity similar to that of a magainin derivative against four bacterial species, incl
78  defense antimicrobial peptides, buforin and magainin, display moderately better protease stability w
79 that are lysed or porous, demonstrating that magainin disruption is a highly stochastic process.
80 e substitution analogue of magainin-2 amide (magainin-F12W, N22C; denoted here as mag-N22C), and a di
81             PGLa, a 21-residue member of the magainin family of antibiotic peptides, is shown to be h
82 n as a synthetic analog to peptides from the magainin family.
83                                 But overall, magainin follows the same all-or-none kinetic model as c
84 clearly indicating that both alamethicin and magainin form pores in membranes but of different sizes.
85                                              Magainin, found in the skin of Xenopus laevis, belongs t
86  the role of self-association in determining magainin function.
87 ed to be distinct from that involved in PGLa-magainin heterodimers.
88 rall goal of this study was to apply the AMP magainin I as a recognition element for Escherichia coli
89 ere used to demonstrate that the immobilized magainin I can bind Salmonella with detection limits sim
90                               We immobilized magainin I on silanized glass slides using biotin-avidin
91      The semiselective antimicrobial peptide magainin I--which occurs naturally on the skin of Africa
92 f the wild type (wt) to other CAMPs, such as Magainin II amide, hNP1-3, LL-37, and lactoferrin.
93 e membrane anchored by antimicrobial peptide magainin II and a phosphatidylethanolamine lipid derivat
94 er library of stapled AMPs (StAMPs) based on magainin II and applied the insights from structure-func
95 pticin, indolicidin, puroindoline A peptide, magainin II F5W, lactoferrampin B, MIP3alpha51-70, and h
96                                 Melittin and magainin II were the most reactive peptides, with signif
97 of several natural AMPs (indolicidin, LL-37, magainin II, and aurein 2.2) causes substantial growth a
98      The peptides examined include melittin, magainin II, PGLa, LAK1, LAK3 and penetratin.
99 : lysine for melittin; serine and lysine for magainin II.
100 , antibiotics, and the antimicrobial peptide magainin, indicating that the degP phenotype was not lim
101                   Data from alamethicin- and magainin-induced pores are presented.
102                          We demonstrate that magainin-induced pores in lipid vesicles have a mean dia
103 ectron microscopy, we have directly observed magainin interacting with synthetic DMPC/DMPG membranes.
104                    Other peptides, including magainins, melittin and protegrins, all appear to induce
105                                              Magainin monomers play the role of fillers in the expans
106 id interactions of two synthetic variants of magainins (MSI-78 and MSI-594) originally designed by Ge
107 nted circular dichroism has detected helical magainin oriented perpendicular to the plane of the memb
108              The effect is most prominent in magainin patterns, which are used to demonstrate the met
109                                              Magainin pores exhibit intermembrane correlations.
110 distinct bound states in lipid bilayers like magainins, protegrins, alamethicin, and melittin that we
111 duced it into a phoP mutant and selected for magainin-resistant clones.
112                               Conjugation to magainin resulted in the considerable strengthening of t
113                                         When magainin samples were further dehydrated or cooled, the
114 ated analogues in the buforin and two in the magainin series were prepared and analyzed for (1) their
115 ve molecules, including pore-forming peptide magainin, the turmeric (curry) extract curcumin, and det
116                         Direct attachment of magainin to the substrate surface not only decreased non
117 s accelerated when the antimicrobial peptide magainin was used to anchor trivalent recognition, or wh
118 milies such as cathelicidins, cecropins, and magainins we demonstrate that designed antagonists can c
119 amethicin and that to the toroidal model for magainin were reviewed.

 
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