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Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/72971/1/j.1553-2712.1999.tb01228.x.pd
Physics of thin-film ferroelectric oxides
This review covers the important advances in recent years in the physics of
thin film ferroelectric oxides, the strongest emphasis being on those aspects
particular to ferroelectrics in thin film form. We introduce the current state
of development in the application of ferroelectric thin films for electronic
devices and discuss the physics relevant for the performance and failure of
these devices. Following this we cover the enormous progress that has been made
in the first principles computational approach to understanding ferroelectrics.
We then discuss in detail the important role that strain plays in determining
the properties of epitaxial thin ferroelectric films. Finally, we look at the
emerging possibilities for nanoscale ferroelectrics, with particular emphasis
on ferroelectrics in non conventional nanoscale geometries.Comment: This is an invited review for Reviews of Modern Physics. We welcome
feedback and will endeavour to incorporate comments received promptly into
the final versio
Functional characterisation of murine gammaherpesvirus 68 glycoprotein 150
Murine gammaherpesvirus 68 (MHV-68) is a B cell tropic pathogen of small rodents
which shares genetic and pathobiological similarities with Epstein-Barr virus (EBV)
and Kaposi's sarcoma associated herpesvirus (KSHV). Unlike EBV and KSHV,
MHV-68 replicates well in vitro and infects inbred mice making it a valuable and
amenable model for the study of gammaherpesvirus replication and their interaction
with the host. Glycoprotein 150 (gpl50) is a virion membrane glycoprotein of
MHV-68 that shares similarities with gp340/220 a membrane glycoprotein of EBV
which facilitates EBV attachment to B cells. Antibodies against gpl50 have been
reported to neutralise MHV-68 infection. The aim of this study was to determine the
function of gpl50 and latterly to assess the potential of gpl50 as a vaccine antigen to
prime and protect inbred mice against MHV-68 infection. For functional studies of
gpl50 two main strategies were adopted; (i) the production of a recombinant virus in
which the gene encoding gpl50 is made dysfunctional resulting in a gpl50
'knockout' (KO) virus and (ii) generation and use of purified gpl50 in cell binding
studies to determine if gpl50 can bind to cells. Recombinant viruses were generated;
virus induced plaques expressing the green fluorescent protein, used as a marker
gene for identification of recombinant viruses, were observed. However, no viruses
in which the required deletion of the gpl50 gene had occurred were isolated. A
gpl50-His fusion protein (gpl50-His) consisting of the extracellular domain of
gpl50 attached to a hexahistidine residue was successfully cloned, expressed in
bacteria and purified. Similarly, a glutathione-S-transferase-His (GST-His) fusion
protein was generated to be used as a control in binding studies. No significant
binding of gpl50-His to murine epithelial cells was detected in an enzyme linked
immunosorbent assay (ELISA) or by fluorescent associated cell sorting (FACS)
analysis. In contrast, significant binding of gpl50-His to primary splenocytes was
shown by FACS analysis. Gpl50-His also bound to purified splenic B cells and both
CD19+ (B cells) and CD 19" splenocytes. Antibodies against gpl50 failed to block
binding of MHV-68 to murine epithelial cells. Results indicate that gpl50-His binds
the heterogeneous splenic cell population as a whole i.e. not a particular subset of
lymphocytes. This suggests gpl50 may interact with a ubiquitous cell surface
protein or perhaps a protein specific to leukocytes and could be involved in MHV-68
attachment to these cells. Gene gun nucleic acid immunisation of inbred mice with a
plasmid encoding gpl50 under the control of a constitutive promoter, alone or in
combination with a recombinant vaccinia virus expressing gpl50 (VVᵍᵖ¹⁵⁰) was
undertaken followed by intranasal challenge with MHV-68. Virus specific antibody
appeared earlier in the group that received gpl50 DNA plus VVᵍᵖ¹⁵⁰. The groups
that received gpl50 DNA in conjunction with either VVᵍᵖ¹⁵⁰ or a control vaccinia
virus (VVgpt) appeared to have reduced levels of latently infected cells in the spleen
day 15 post infection and reduced splenomegaly (a phenomenon of MHV-68
infection) in comparison with control mice. This could indicate that vaccinia virus,
in a non-specific manner, boosts the specific immune response to previously
administered DNA and in this case was able to limit the level of MHV-68 reaching
the spleen. However, this vaccine regimen failed to significantly alter the level of
infectious virus in the lung or prevent the establishment of latent virus in the spleen
Statistical switching kinetics in ferroelectrics
By assuming a more realistic nucleation and polarization reversal scenario we
build a new statistical switching model for ferroelectrics, which is different
from either the Kolmogorov-Avrami-Ishibashi (KAI) model or the
Nucleation-Limited-Switching (NLS) model. After incorporating a time-dependent
depolarization field this model gives a good description about the retardation
behavior in polycrystalline thin films at medium or low fields, which can not
be described by the traditional KAI model. This model predicts correctly n=1
for polycrystalline thin films at high Eappl or ceramic bulks in the ideal
case
Unusual behaviour of the ferroelectric polarization in PbTiO/SrTiO superlattices
Artificial PbTiO/SrTiO superlattices were constructed using
off-axis RF magnetron sputtering. X-ray diffraction and piezoelectric atomic
force microscopy were used to study the evolution of the ferroelectric
polarization as the ratio of PbTiO to SrTiO was changed. For
PbTiO layer thicknesses larger than the 3-unit cells SrTiO
thickness used in the structure, the polarization is found to be reduced as the
PbTiO thickness is decreased. This observation confirms the primary role
of the depolarization field in the polarization reduction in thin films. For
the samples with ratios of PbTiO to SrTiO of less than one a
surprising recovery of ferroelectricity that cannot be explained by
electrostatic considerations was observed
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