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1 n the capsid proteins and the genomic RNA of bacteriophage MS2.
2  three well-characterized model proteins and bacteriophage MS2.
3 virions of Herpes Simplex Type 1 viruses and bacteriophage MS2.
4 de display platform based on VLPs of the RNA bacteriophage MS2.
5 vaccine development based on the VLPs of RNA bacteriophage MS2.
6  translational operator stem-loop of the RNA bacteriophage MS2.
7 3 viral capsid, during reassembly of the RNA bacteriophage MS2.
8 esized and coupled to chymotrypsinogen A and bacteriophage MS2.
9 immunoassay has been developed for detecting bacteriophage MS2.
10 ion within the 3569-nucleotide RNA genome of bacteriophage MS2.
11 o model microorganisms: Escherichia coli and bacteriophage MS2.
12 achieved by columns for the bacterial virus (bacteriophage) MS2 110 (+/-19)%, as model organism, as w
13 eating of a suspension of a model virus, RNA bacteriophage MS2, 13 chemical digestion products were d
14  (99.99%+), moderately effective in reducing bacteriophage MS2 (99%+), and somewhat effective against
15 man blood, using a novel LAMP primer set for bacteriophage MS2 (a model RNA virus particle).
16 f of concept for the label-free detection of bacteriophage MS2, a model indicator of microbiological
17 gly similar to that previously observed with bacteriophage MS2, a phylogenetically distinct virus wit
18 chitectures to develop immunosensors for the bacteriophage MS2, a virus often detected in sewage-impa
19 sunlight inactivation of single-stranded RNA bacteriophage MS2, a widely used surrogate, and hNoV GII
20  3 (PV3), adenovirus type 2 (HAdV2), and two bacteriophage (MS2 and PRD1) was investigated in an arra
21  the viral genome, as exemplified by the RNA bacteriophage MS2 and as proposed for other RNA viruses
22                     Recombinant forms of the bacteriophage MS2 and its RNA-free (empty) MS2 capsid we
23 ation allowed for the discrimination between bacteriophage MS2 and other closely related RNA bacterio
24 extraction and amplification efficiency (the bacteriophage MS2 and phocine herpesvirus).
25          In simple ssRNA viruses such as the bacteriophage MS2 and small RNA plant viruses such as ST
26 ruses (MHV and varphi6) and two nonenveloped bacteriophages (MS2 and T3) in raw wastewater samples.
27 improved removal of about 4-log in regard to bacteriophages MS2 and PhiX174.
28 partite BMV viral capsid and the monopartite bacteriophages MS2 and Qbeta for which a dominant RNA co
29 activation of three-human adenovirus and two bacteriophages-MS2 and phiX174-in surface waters and was
30 igated the inactivation of Escherichia coli, bacteriophage MS2, and Bacillus subtilis spores as surro
31 strated here with tobacco mosaic virus U2, a bacteriophage MS2, and equine encephalitis TRD, is achie
32 s capsids, focusing on hepatitis B virus and bacteriophage MS2, and formation of glycoproteins in the
33 ally, the non-enveloped, double-stranded DNA bacteriophage MS2, and the Gram-negative E. coli and Gra
34 ularly imprinted polymer (MIP) targeting the bacteriophage MS2 as the template was investigated using
35  5% sodium chloride aerosol, and aerosolized bacteriophage MS2 between patient beds 3 meters apart an
36 be the cryo-electron microscopy structure of bacteriophage MS2 bound to its receptor, the bacterial F
37 e, the detection limit for quantification of bacteriophage MS2 by quantitative reverse transcriptase
38 we demonstrated the DESI-MS detection of the bacteriophage MS2 capsid protein from crude samples with
39  RNA hairpin containing the binding site for bacteriophage MS2 capsid protein.
40  the three-dimensional solution structure of bacteriophage MS2 capsids reassembled from recombinant p
41 single-stranded RNA (ssRNA) viruses, such as bacteriophage MS2, co-assemble their capsid with the gen
42 mes containing binding sites for BglG or the bacteriophage MS2 coat protein along with 2 fluorescent
43 sible to generate crosslinks between the RNA bacteriophage MS2 coat protein and the initiator stem-lo
44 roteins containing an RS domain fused to the bacteriophage MS2 coat protein are sufficient to activat
45 red assembly and solubility properties using bacteriophage MS2 coat protein as a model self-associati
46                           We have found that bacteriophage MS2 coat protein binds several Escherichia
47 that such quasi-equivalent conformers of RNA bacteriophage MS2 coat protein dimers (CP(2)) can be swi
48 g sequences and detected by co-expression of bacteriophage MS2 coat protein fused with EGFP.
49 ay, in which a fusion protein of PTB and the bacteriophage MS2 coat protein is recruited to a splicin
50 en the F and G beta strands (FG loop) of the bacteriophage MS2 coat protein subunit forms inter-subun
51 ed the kinetics of complex formation between bacteriophage MS2 coat protein subunits and synthetic RN
52                    We assayed the ability of bacteriophage MS2 coat protein to package large, defined
53  of the high sequence coverage obtained, the bacteriophage MS2 coat protein was identified with high
54 rform in-cellulo packaging experiments using bacteriophage MS2 coat proteins and a variety of RNA mol
55 ively expressing an ASH1 mRNA containing the bacteriophage MS2 coat-protein binding site adjacent to
56                Across the model proteins and bacteriophage MS2 (coat protein), differing widely in st
57 recent cryo-electron microscopy structure of bacteriophage MS2, determined with only 5-fold symmetry
58                     Whereas common surrogate bacteriophage MS2 does not serve as a conservative chlor
59 ystematically studied the adsorption of four bacteriophages (MS2, fr, GA, and Qbeta) to five model su
60 ynamics of negatively charged viruses (i.e., bacteriophages MS2, fr, GA, and Qbeta) and polystyrene n
61                          The coat protein of bacteriophage MS2 functions as a symmetric dimer to bind
62 from RNA footprinting in situ reveal how the bacteriophage MS2 genome regulates both particle assembl
63 one of four classes of biothreat agents, and bacteriophage MS2 has been used as a simulant for biothr
64  microorganisms, as well as for detection of bacteriophage MS2 in the presence of a large excess of E
65                                              Bacteriophage MS2 is a positive-sense, single-stranded R
66 w functionalization strategies, detection of bacteriophage MS2 is performed through either a direct a
67         The target of the fourth Sgl, L from bacteriophage MS2, is still unknown, but we review evide
68 zed using diverse techniques, the use of the bacteriophage MS2 method to encode genetically fluoresce
69 usly quantify airborne concentrations of the bacteriophage MS2 near the oral cavity of a dental manne
70  5% sodium chloride aerosol, and aerosolized bacteriophage MS2 released from the inner bed were carri
71 of 40 nm nominal pore size was used to study bacteriophage MS2 removal under different membrane condi
72 dated larger sample volumes in extraction of bacteriophage MS2 RNA from the various specimen matrices
73 est, including the long noncoding RNA NORAD, bacteriophage MS2 RNA, and human telomerase RNA, and we
74 e determined the secondary structures of the bacteriophage MS2 ssRNA genome (gRNA) frozen in defined
75 sed RNA oligomer segments from the genome of bacteriophage MS2 to UV254, simulated sunlight, and sing
76 surrogate viruses murine norovirus (MNV) and bacteriophage MS2 under identical experimental condition
77 tivation rates for a common surrogate virus, bacteriophage MS2 (up to 270% compared to the unmodified
78  the total damage incurred by a model virus (bacteriophage MS2) upon inactivation induced by five com
79 ckaging of a representative ssRNA virus, the bacteriophage MS2, via a series of biomolecular simulati
80 he device can capture and keep a bioaerosol (bacteriophage MS2) viable for downstream analysis.
81  + 8H]8+ to [M + 6H]6+ precursor ions of the bacteriophage MS2 viral coat protein following concentra
82   Applying the model to the test case of the bacteriophage MS2 virus, I show that the models ability
83 es covalently conjugated to the surface of a bacteriophage MS2 VLP.
84                                              Bacteriophage MS2 was aggregated by lowering the solutio
85 A full-length cDNA copy of the RNA genome of bacteriophage MS2 was assembled by the in-frame ligation
86                                              Bacteriophage MS2 was found to have a mobility diameter
87 oop (TR) encompassing 19 nt of the genome of bacteriophage MS2 was shown to act as an allosteric effe
88                                              Bacteriophage MS2 was used as a viral tracer and fluores
89                                        Using bacteriophage MS2, we demonstrate here via a combination
90                                          For bacteriophage MS2, we have shown that collapse is driven
91                                              Bacteriophages MS2 were spiked in tap water and concentr
92 xtrinsic controls (phocine herpesvirus 1 and bacteriophage MS2) were included to ensure extraction an
93 cept, I design a polycistronic mRNA based on bacteriophage MS2, where the upstream gene is capable of
94  case study, we consider the viral capsid of bacteriophage MS2, which is formed from 60 asymmetric (A
95 is system is the spherical protein capsid of bacteriophage MS2, which was used to house gold particle