ライフサイエンスコーパス: bacterial outer membrane

1 racted the IgA1 protease preprotein from the bacterial outer membrane.

2 on of lipid II perturbs the structure of the bacterial outer membrane.

3 of targeting of beta-barrel proteins to the bacterial outer membrane.

4 ilitating their own translocation across the bacterial outer membrane.

5 t overcome noxious compounds that damage the bacterial outer membrane.

6 oxygen production in the surroundings of the bacterial outer membrane.

7 ability of these types of drugs to cross the bacterial outer membrane.

8 allows diffusion of small solutes across the bacterial outer membrane.

9 pecific 5',3'-nucleotidases localized to the bacterial outer membrane.

10 s primarily through pores or channels in the bacterial outer membrane.

11 dD, a putative lipoprotein, localized to the bacterial outer membrane.

12 rt of small hydrophobic molecules across the bacterial outer membrane.

13 lity to drive their own secretion across the bacterial outer membrane.

14 the mechanism of colicin import through the bacterial outer membrane.

15 PS in the outer leaflet of the Gram-negative bacterial outer membrane.

16 lebs indicate that the blebs derive from the bacterial outer membrane.

17 1969, I became interested in the function of bacterial outer membranes, a line of work that led to th

18 (U) into the host cell and expression of the bacterial outer membrane adhesin, intimin.

19 However, other cellular receptors or bacterial outer membrane adhesins essential for this pro

20 ort function and attaches the adhesin to the bacterial outer membrane after export is complete.

21 Rd/HapS243A, resulted in loss of Hap in the bacterial outer membrane and a decrease in hap transcrip

22 36 protein was exposed on the surface of the bacterial outer membrane and bound to the host extracell

23 ed early (15 min and 1 hr) disruption of the bacterial outer membrane and cell wall, as demonstrated

24 des possessing both enhanced mobility in the bacterial outer membrane and spatial structure facilitat

25 tein interacts with the inner leaflet of the bacterial outer membrane and that the two monomers provi

26 ormation of a direct interaction between the bacterial outer membrane and the plasma membrane of ME18

27 rides (LOS) are the main lipid components of bacterial outer membranes and are essential for cell via

28 es with lipopolysaccharides of Gram-negative bacterial outer membranes and find that lipopolysacchari

29 e micelles associate non-covalently with the bacterial outer-membrane and that this interaction incre

30 s such as LPS, a glycolipid component of the bacterial outer membrane, and formylated peptides (fMLP)

31 that TspO normally forms a dimer within the bacterial outer membrane, and the dimer form of TspO may

32 biochemical, and antigenic properties of the bacterial outer membrane are profoundly influenced by th

33 al translocator domain that inserts into the bacterial outer membrane as a beta-barrel structure and

34 was shown to retain its structure within the bacterial outer membrane as assayed by its binding prope

35 l fluorescent imaging of the dynamics of the bacterial outer membrane as cells divide.

36 ound that the asymmetry of the Gram-negative bacterial outer membrane as well as the TM residues of a

37 The functional properties of two bacterial outer-membrane beta-barrel proteins, OmpT and

38 y help us to understand important aspects of bacterial outer membrane biogenesis, but also have signi

39 e insertion of beta-barrel proteins into the bacterial outer membrane, but it is unclear whether it t

40 se incorporating lipopolysaccharide, a major bacterial outer membrane component) and induce a compara

41 ling and on innate inflammatory responses to bacterial outer membrane components, including purified

42 studied; however, the contribution of other bacterial outer membrane components, such as Braun (mure

43 The bacterial outer membrane comprises two main classes of c

44 ccharide (LPS), a component of Gram-negative bacterial outer membranes, comprises three regions: lipi

45 ollowing release of these molecules from the bacterial outer membrane during cell division or attack

46 ed in formation of lipopolysaccharide in the bacterial outer membrane), ebgR (lactose utilization rep

47 e OspE1/OspE2 proteins were localized to the bacterial outer membrane following exposure to bile salt

48 e; the insertion of the pore domain into the bacterial outer membrane follows the rules of beta-barre

49 The Gram-negative bacterial outer membrane fortifies the cell against envi

50 ic, major, integral protein component of the bacterial outer membrane, functions as a critical determ

51 tes the assembly of the T3SS secretin in the bacterial outer membrane, highlighting the molecular rol

52 robably contribute to the remodelling of the bacterial outer membrane in response to the host environ

53 al peptide, this protein is localized on the bacterial outer membrane, indicating that it is transpor

54 The understanding of the Gram-negative bacterial outer membrane is therefore critical to develo

55 The assembly of proteins into bacterial outer membranes is a key cellular process that

56 ExsB, a lipoprotein localized in the bacterial outer membrane, is one of the components of th

57 e insertion of proteins in the gram-negative bacterial outer membrane, is the surface molecule recogn

58 Bacterial outer membrane lipopolysaccharide (LPS) potent

59 The peptide is reconstituted in bacterial outer membrane lipopolysaccharide extract as w

60 ts of eukaryotic membranes (cholesterol) and bacterial outer membranes (lipopolysaccharide or LPS).

61 iderophore transporters of the Gram-negative bacterial outer membrane manifest a unique architecture:

62 t to sporulation as a mechanism by which the bacterial outer membrane may have arisen and A. longum a

63 Zot localizes in the bacterial outer membrane of V. cholerae with subsequent

64 ide (CAMP) antibiotic that permeabilizes the bacterial outer membrane (OM) and has been used to treat

65 The bacterial outer membrane (OM) is a barrier containing me

66 The Gram-negative bacterial outer membrane (OM) is a unique bilayer that f

67 lly consists of a transporter located in the bacterial outer membrane (OM) which is responsible for t

68 nslocation intermediates associated with the bacterial outer membrane (OM), we generated constructs i

69 locate their N-terminal passenger across the bacterial outer membrane (OM).

70 ibutes to the stability and integrity of the bacterial outer membrane (OM).

71 rfamily, and seven families of Gram-negative bacterial outer membrane porins, largely account for the

72 e substrate exhibiting high activity for the bacterial outer-membrane protease (OmpT).

73 The bacterial outer membrane protein G (OmpG), a monomeric p

74 e of host cells, where it interacts with the bacterial outer membrane protein intimin and triggers ce

75 Interaction of translocated Tir with the bacterial outer membrane protein intimin is required to

76 asma membrane and clustered upon binding the bacterial outer membrane protein intimin.

77 into nonphagocytic cells is mediated by the bacterial outer membrane protein invasin.

78 The bacterial outer membrane protein OmpA is one of the few

79 in and lipid on the folding mechanism of the bacterial outer membrane protein PagP.

80 Intimin is a bacterial outer membrane protein required for intimate a

81 o hypothesize that TP0453 is a novel type of bacterial outer membrane protein which may render the T.

82 vent is mediated, in part, by binding of the bacterial outer membrane protein, intimin, to a second E

83 osphorylated; and (iii) interacting with the bacterial outer membrane protein, intimin.

84 e energy landscape for the dimerization of a bacterial outer membrane protein, NanC, in a phospholipi

85 Using the bacterial outer-membrane protein OmpX as an example, we

86 oprotein (PAL) is a ubiquitous gram-negative bacterial outer-membrane protein that is shed by bacteri

87 BtuB is a bacterial outer-membrane protein that transports vitamin

88 Recombinant OmpW antigen (a bacterial outer-membrane protein) of V. cholerae was exp

89 Almost all bacterial outer membrane proteins (OMPs) contain a beta

90 g bacteria bound to at least three conserved bacterial outer membrane proteins (OMPs), but not LPS, a

91 Bacterial outer membrane proteins A and C co-purify in l

92 pid bilayer via transmembrane alpha-helices, bacterial outer membrane proteins adopt a beta-barrel ar

93 NanC is a member of the KdgM-family of bacterial outer membrane proteins and is responsible for

94 design of biological nanopores is focused on bacterial outer membrane proteins and pore-forming toxin

95 he phagosome, following interaction with the bacterial outer membrane proteins OmpC and OmpF.

96 Ushers constitute a family of bacterial outer membrane proteins responsible for the as

97 Secretins are bacterial outer membrane proteins that are important for

98 TonB-dependent transporters (TBDTs) are bacterial outer membrane proteins that bind and transpor

99 Autotransporters are bacterial outer membrane proteins that consist of a larg

100 Crystal structures have been solved for two bacterial outer membrane proteins, FhuA and FepA, which

101 r substitutions that do not occur in natural bacterial outer membrane proteins, we succeeded in engin

102 enylalanine, which is highly conserved among bacterial outer membrane proteins.

103 us encoded a protein with characteristics of bacterial outer membrane proteins.

104 Prior studies indicate that 3 bacterial outer-membrane proteins (OMPs) are released in

105 ng proteins, haem may be transported via the bacterial outer membrane receptor into the cell.

106 s of siderophores covalently linked to their bacterial outer membrane receptors represent a credible

107 ism by which TcpF is translocated across the bacterial outer membrane requires the TCP biogenesis mac

108 A search for the TSF binding targets on the bacterial outer membrane resulted in identification of P

109 y mediate their own translocation across the bacterial outer membrane: the carboxy-terminal beta doma

110 Attached to the bacterial outer membrane, these new cell wall components

111 posed that the phage are extruded across the bacterial outer membrane through pIV channels.

112 that hopanoids interact with glycolipids in bacterial outer membranes to form a highly ordered bilay

113 nzymes and filamentous bacteriophages across bacterial outer membranes to the extracellular milieu.

114 The binding and recognition of ligands by bacterial outer membrane transport proteins is mediated

115 selected sites within the beta-barrel of the bacterial outer-membrane transport protein BtuB by site-

116 ompare transmembrane signaling events in the bacterial outer-membrane transport proteins BtuB, FecA,

117 The bacterial outer membrane transporter for vitamin B(12),

118 n tissue and most likely in the form of shed bacterial outer membrane vesicles ("blebs"), we examined

119 is translocated into the host cytoplasm via bacterial outer membrane vesicles (OMV).

120 We have engineered bacterial outer membrane vesicles (OMVs) with dramatical

121 Our results demonstrate that production of bacterial outer membrane vesicles is a fully independent

122 st a novel role of BPI in the interaction of bacterial outer membrane vesicles with dendritic cells t

123 th use of reverse vaccinology) combined with bacterial outer-membrane vesicles.

124 The bacterial outer-membrane vitamin B(12) transporter, BtuB

125 lecular forms of Tpr are associated with the bacterial outer membrane where they are likely responsib

126 ce arises through charge modification of the bacterial outer membrane with the attachment of the cati

127 membrane vesicle (OMV) which is composed of bacterial outer membrane wrapped around contents of the