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1 rt of small hydrophobic molecules across the bacterial outer membrane.
2 lity to drive their own secretion across the bacterial outer membrane.
3  the mechanism of colicin import through the bacterial outer membrane.
4 lebs indicate that the blebs derive from the bacterial outer membrane.
5 racted the IgA1 protease preprotein from the bacterial outer membrane.
6 on of lipid II perturbs the structure of the bacterial outer membrane.
7  of targeting of beta-barrel proteins to the bacterial outer membrane.
8 nute spherical structures emanating from the bacterial outer membrane.
9 phobic saccharolipid that anchors LPS to the bacterial outer membrane.
10 N-terminal translocation of P.69T across the bacterial outer membrane.
11 ane GldL/PorL ring to drive processes at the bacterial outer membrane.
12 embrane beta-barrel proteins (OMPs) into the bacterial outer membrane.
13 t overcome noxious compounds that damage the bacterial outer membrane.
14 PS in the outer leaflet of the Gram-negative bacterial outer membrane.
15 ilitating their own translocation across the bacterial outer membrane.
16 oxygen production in the surroundings of the bacterial outer membrane.
17 ability of these types of drugs to cross the bacterial outer membrane.
18 allows diffusion of small solutes across the bacterial outer membrane.
19 pecific 5',3'-nucleotidases localized to the bacterial outer membrane.
20 s primarily through pores or channels in the bacterial outer membrane.
21 dD, a putative lipoprotein, localized to the bacterial outer membrane.
22 e by wrapping synthetic polymeric cores with bacterial outer membranes.
23 tes in lipopolysaccharide (LPS) molecules in bacterial outer membranes.
24 popolysaccharides are critical components of bacterial outer membranes.
25 1969, I became interested in the function of bacterial outer membranes, a line of work that led to th
26 the ligand gated porins of the Gram-negative bacterial outer membrane actively acquire the resulting
27 (U) into the host cell and expression of the bacterial outer membrane adhesin, intimin.
28         However, other cellular receptors or bacterial outer membrane adhesins essential for this pro
29 ort function and attaches the adhesin to the bacterial outer membrane after export is complete.
30  Rd/HapS243A, resulted in loss of Hap in the bacterial outer membrane and a decrease in hap transcrip
31 36 protein was exposed on the surface of the bacterial outer membrane and bound to the host extracell
32 ed early (15 min and 1 hr) disruption of the bacterial outer membrane and cell wall, as demonstrated
33 pture the structure and function of Ail in a bacterial outer membrane and set the stage for probing i
34 des possessing both enhanced mobility in the bacterial outer membrane and spatial structure facilitat
35 tein interacts with the inner leaflet of the bacterial outer membrane and that the two monomers provi
36 ormation of a direct interaction between the bacterial outer membrane and the plasma membrane of ME18
37 rides (LOS) are the main lipid components of bacterial outer membranes and are essential for cell via
38 es with lipopolysaccharides of Gram-negative bacterial outer membranes and find that lipopolysacchari
39 spects of the biological complexity found in bacterial outer membranes and, by doing so, offers a pow
40 e micelles associate non-covalently with the bacterial outer-membrane and that this interaction incre
41 s such as LPS, a glycolipid component of the bacterial outer membrane, and formylated peptides (fMLP)
42  that TspO normally forms a dimer within the bacterial outer membrane, and the dimer form of TspO may
43 biochemical, and antigenic properties of the bacterial outer membrane are profoundly influenced by th
44 al translocator domain that inserts into the bacterial outer membrane as a beta-barrel structure and
45 was shown to retain its structure within the bacterial outer membrane as assayed by its binding prope
46 l fluorescent imaging of the dynamics of the bacterial outer membrane as cells divide.
47 ound that the asymmetry of the Gram-negative bacterial outer membrane as well as the TM residues of a
48  small molecular-weight, covalently attached bacterial outer membrane-associated lipid that is requir
49             The functional properties of two bacterial outer-membrane beta-barrel proteins, OmpT and
50 y help us to understand important aspects of bacterial outer membrane biogenesis, but also have signi
51                            TamB functions in bacterial outer membrane biogenesis.
52 e insertion of beta-barrel proteins into the bacterial outer membrane, but it is unclear whether it t
53 GBPs facilitate sensing of the gram-negative bacterial outer membrane component lipopolysaccharide (L
54 se incorporating lipopolysaccharide, a major bacterial outer membrane component) and induce a compara
55 ling and on innate inflammatory responses to bacterial outer membrane components, including purified
56  studied; however, the contribution of other bacterial outer membrane components, such as Braun (mure
57 lysaccharide biosynthesis, and biogenesis of bacterial outer-membrane components, like lipopolysaccha
58                                          The bacterial outer membrane comprises two main classes of c
59 ccharide (LPS), a component of Gram-negative bacterial outer membranes, comprises three regions: lipi
60 ollowing release of these molecules from the bacterial outer membrane during cell division or attack
61 ed in formation of lipopolysaccharide in the bacterial outer membrane), ebgR (lactose utilization rep
62 ssembly is membrane-assisted: Increasing the bacterial outer membrane fluidity decreases the populati
63 e OspE1/OspE2 proteins were localized to the bacterial outer membrane following exposure to bile salt
64 e; the insertion of the pore domain into the bacterial outer membrane follows the rules of beta-barre
65 provide insight into the permeability of the bacterial outer membrane for assessing lignin fragment u
66                            The Gram-negative bacterial outer membrane fortifies the cell against envi
67 ic, major, integral protein component of the bacterial outer membrane, functions as a critical determ
68 tes the assembly of the T3SS secretin in the bacterial outer membrane, highlighting the molecular rol
69 robably contribute to the remodelling of the bacterial outer membrane in response to the host environ
70 al peptide, this protein is localized on the bacterial outer membrane, indicating that it is transpor
71 e, the permeability of fosfomycin across the bacterial outer membrane is largely unexplored.
72                                          The bacterial outer membrane is the first line of defence ag
73       The understanding of the Gram-negative bacterial outer membrane is therefore critical to develo
74                The assembly of proteins into bacterial outer membranes is a key cellular process that
75         ExsB, a lipoprotein localized in the bacterial outer membrane, is one of the components of th
76 e insertion of proteins in the gram-negative bacterial outer membrane, is the surface molecule recogn
77 oes not only compromise the integrity of the bacterial outer-membrane, it also deactivates efflux pum
78                                              Bacterial outer membrane lipopolysaccharide (LPS) potent
79              The peptide is reconstituted in bacterial outer membrane lipopolysaccharide extract as w
80 ts of eukaryotic membranes (cholesterol) and bacterial outer membranes (lipopolysaccharide or LPS).
81 iderophore transporters of the Gram-negative bacterial outer membrane manifest a unique architecture:
82 t to sporulation as a mechanism by which the bacterial outer membrane may have arisen and A. longum a
83 tions, we created a surface-supported planar bacterial outer membrane model on an optically-transpare
84 nin-related compounds across a gram-negative bacterial outer membrane model.
85                     Glycan uptake across the bacterial outer membrane of these bacteria is mediated b
86                         Zot localizes in the bacterial outer membrane of V. cholerae with subsequent
87 ide (CAMP) antibiotic that permeabilizes the bacterial outer membrane (OM) and has been used to treat
88  well established that colistin disrupts the bacterial outer membrane (OM) by selectively targeting l
89                                          The bacterial outer membrane (OM) is a barrier containing me
90                            The Gram-negative bacterial outer membrane (OM) is a unique bilayer that f
91 integration of beta-barrel proteins into the bacterial outer membrane (OM) is catalysed by the beta-b
92 sertion of lipopolysaccharide (LPS) into the bacterial outer membrane (OM) is mediated by a druggable
93 embly at the surfaces-exposed leaflet of the bacterial outer membrane (OM) is mediated by the OM LPS
94 possible to obtain structural information on bacterial outer membrane (OM) proteins in intact cells f
95                   The extracellular loops of bacterial outer membrane (OM) transporters are thought t
96 lly consists of a transporter located in the bacterial outer membrane (OM) which is responsible for t
97 nslocation intermediates associated with the bacterial outer membrane (OM), we generated constructs i
98 ia maintains the integrity of the asymmetric bacterial outer membrane (OM).
99 locate their N-terminal passenger across the bacterial outer membrane (OM).
100 ibutes to the stability and integrity of the bacterial outer membrane (OM).
101 rfamily, and seven families of Gram-negative bacterial outer membrane porins, largely account for the
102 opolysaccharide (LPS) from the Gram-negative bacterial outer membrane potently activates the human in
103 e substrate exhibiting high activity for the bacterial outer-membrane protease (OmpT).
104                                          The bacterial outer membrane protein G (OmpG), a monomeric p
105 e of host cells, where it interacts with the bacterial outer membrane protein intimin and triggers ce
106     Interaction of translocated Tir with the bacterial outer membrane protein intimin is required to
107 asma membrane and clustered upon binding the bacterial outer membrane protein intimin.
108  into nonphagocytic cells is mediated by the bacterial outer membrane protein invasin.
109 n of the cell surface protein CD150 with the bacterial outer membrane protein Omp25, inducing efficie
110                                          The bacterial outer membrane protein OmpA is one of the few
111 in and lipid on the folding mechanism of the bacterial outer membrane protein PagP.
112                                 Intimin is a bacterial outer membrane protein required for intimate a
113 o hypothesize that TP0453 is a novel type of bacterial outer membrane protein which may render the T.
114 vent is mediated, in part, by binding of the bacterial outer membrane protein, intimin, to a second E
115 osphorylated; and (iii) interacting with the bacterial outer membrane protein, intimin.
116 e energy landscape for the dimerization of a bacterial outer membrane protein, NanC, in a phospholipi
117                                    Using the bacterial outer-membrane protein OmpX as an example, we
118 oprotein (PAL) is a ubiquitous gram-negative bacterial outer-membrane protein that is shed by bacteri
119                                    BtuB is a bacterial outer-membrane protein that transports vitamin
120                  Recombinant OmpW antigen (a bacterial outer-membrane protein) of V. cholerae was exp
121  chaperone network ensures the biogenesis of bacterial outer membrane proteins (OMPs) and has recentl
122                                   Almost all bacterial outer membrane proteins (OMPs) contain a beta
123                                              Bacterial outer membrane proteins (OMPs) contain a uniqu
124 ed proteomes to search for homologs of known bacterial outer membrane proteins (OMPs) led to the iden
125 g bacteria bound to at least three conserved bacterial outer membrane proteins (OMPs), but not LPS, a
126 ze the stability and folding kinetics of two bacterial outer membrane proteins (OMPs), OmpA and BamA.
127                                              Bacterial outer membrane proteins A and C co-purify in l
128 pid bilayer via transmembrane alpha-helices, bacterial outer membrane proteins adopt a beta-barrel ar
129       NanC is a member of the KdgM-family of bacterial outer membrane proteins and is responsible for
130 design of biological nanopores is focused on bacterial outer membrane proteins and pore-forming toxin
131 he phagosome, following interaction with the bacterial outer membrane proteins OmpC and OmpF.
132                Ushers constitute a family of bacterial outer membrane proteins responsible for the as
133                                Secretins are bacterial outer membrane proteins that are important for
134      TonB-dependent transporters (TBDTs) are bacterial outer membrane proteins that bind and transpor
135                         Autotransporters are bacterial outer membrane proteins that consist of a larg
136  Crystal structures have been solved for two bacterial outer membrane proteins, FhuA and FepA, which
137 r substitutions that do not occur in natural bacterial outer membrane proteins, we succeeded in engin
138 enylalanine, which is highly conserved among bacterial outer membrane proteins.
139 us encoded a protein with characteristics of bacterial outer membrane proteins.
140 induce functional antibody responses against bacterial outer membrane proteins.
141                Prior studies indicate that 3 bacterial outer-membrane proteins (OMPs) are released in
142 ort of iron-catecholate complexes across the bacterial outer membrane, providing the bacterium with i
143 ng proteins, haem may be transported via the bacterial outer membrane receptor into the cell.
144 s of siderophores covalently linked to their bacterial outer membrane receptors represent a credible
145 efense, and 2) transcriptional repression of bacterial outer membrane receptors required for phage ad
146 ism by which TcpF is translocated across the bacterial outer membrane requires the TCP biogenesis mac
147  A search for the TSF binding targets on the bacterial outer membrane resulted in identification of P
148 y mediate their own translocation across the bacterial outer membrane: the carboxy-terminal beta doma
149                              Attached to the bacterial outer membrane, these new cell wall components
150 posed that the phage are extruded across the bacterial outer membrane through pIV channels.
151  that hopanoids interact with glycolipids in bacterial outer membranes to form a highly ordered bilay
152 nzymes and filamentous bacteriophages across bacterial outer membranes to the extracellular milieu.
153    The binding and recognition of ligands by bacterial outer membrane transport proteins is mediated
154 selected sites within the beta-barrel of the bacterial outer-membrane transport protein BtuB by site-
155 ompare transmembrane signaling events in the bacterial outer-membrane transport proteins BtuB, FecA,
156                                          The bacterial outer membrane transporter for vitamin B(12),
157 n tissue and most likely in the form of shed bacterial outer membrane vesicles ("blebs"), we examined
158  is translocated into the host cytoplasm via bacterial outer membrane vesicles (OMV).
159                                              Bacterial outer membrane vesicles (OMVs) represent an in
160                           We have engineered bacterial outer membrane vesicles (OMVs) with dramatical
161 tline the advantages and challenges to using bacterial outer membrane vesicles (OMVs), nanoscale sphe
162 d A, MPLA) displayed increased biogenesis of bacterial outer membrane vesicles (OMVs).
163 lammation and fibrosis due to the release of bacterial outer membrane vesicles (OMVs).
164 y pathways that can facilitate this process: bacterial outer membrane vesicles (OMVs); the spike (S)
165   Our results demonstrate that production of bacterial outer membrane vesicles is a fully independent
166 st a novel role of BPI in the interaction of bacterial outer membrane vesicles with dendritic cells t
167 esicle species, including enveloped viruses, bacterial outer membrane vesicles, and mammalian extrace
168 th use of reverse vaccinology) combined with bacterial outer-membrane vesicles.
169                                          The bacterial outer-membrane vitamin B(12) transporter, BtuB
170                            The presence of a bacterial outer membrane was detected without extrinsic
171 ivo efficacy, its ability to permeate across bacterial outer membranes was insufficient for further d
172 lecular forms of Tpr are associated with the bacterial outer membrane where they are likely responsib
173 ce arises through charge modification of the bacterial outer membrane with the attachment of the cati
174 nits assemble to form a gated channel in the bacterial outer membrane, with associated soluble domain
175  membrane vesicle (OMV) which is composed of bacterial outer membrane wrapped around contents of the

 
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