Privalsky
Lab. This image shows how a helix 12 at the C-terminus of these receptors
functions as a hormone-regulated "molecular toggle switch;" by altering its conformation,
helix 12 determines whether a corepressor or a coactivator is recruited to the nuclear
receptor.
»Click image for larger version.
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Segal
Lab. This image shows re-engineering the dimerization interface of a zinc
finger nuclease to reduce cytotoxicity.
»Click image for larger version.
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Heyer
Lab. Image of Rad51 filaments on DNA visualized by negative staining in
electron microscopy. Rad51 catalyzes the central reactions in homologous recombination,
homology search and DNA strand invasion. .
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Farnham
Lab. Image shows a technique called ChIP-chip (chromatin immunoprecipitation
followed by microarray analysis) that allows them to investigate chromatin structure
and protein-DNA interactions in living cells or in tumor tissues.
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Kaplan
Lab. A dominant mutation in the adenomatous polyposis coli tumor suppressor
gene causes mitotic abnormalities in human cells. The microtubule (red) spindle
has not properly segregated all the chromosomes (blue), as seen by the kinetochore
positive (green) chromosomes left at the midzone.
»Click image for larger version.
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Model used in Artyom Kopp's laboratory.
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Kaplan
Lab.This shows live-cell imaging in the budding yeast (S. cerevisiae) to
address how a class of kinetochore proteins, kinetochore-passenger proteins, ensure
the proper order of anaphase events.
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Starr
Lab. The position of the nucleus in the cell plays many important roles
in development. Here we show dorsal epidermal nuclei migrating to a new position
in a C. elegans embryo. Green shows the cell-cell boundaries and DAPI stained nuclei
are blue. Antibodies against UNC-83 (red) localize to the nuclear envelope of these
migrating nuclei. UNC-83 is required for these and other nuclear migration events.
For more information, please contact the Starr lab.
»Click image for larger version.
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Hammock
Lab. The image shows the potentially lethal scorpion Parabuthus with a
drop of highly toxic venom. We identify peptide toxins from such venoms by LC coupled
to a hybrid electrospray-time of flight mass spectrometer and study their effect
on vertebrate and insect cells. We express insect specific toxins in baculoviruses
as green approaches to insect pest control. Mammal specific toxins are used as probes
to study the vertebrate nervous system and potential pharmaceutical leads.
»Click image for larger version.
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Williamson
Lab. Root tip of the plant Medicago truncatula stained with a specific
dye for nitric oxide. Nitric oxide is an attractant to plant parasitic nematodes
and probably other organisms that interact with roots.
»Click image for larger version.
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Root
tip of the plant Medicago truncatula stained with a specific dye for nitric oxide.
Nitric oxide is an attractant to plant parasitic nematodes and probably other organisms
that interact with roots.
»Click image for larger version.
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The
image shows the potentially lethal scorpion Parabuthus with a drop of highly toxic
venom. We identify peptide toxins from such venoms by LC coupled to a hybrid electrospray-time
of flight mass spectrometer and study their effect on vertebrate and insect cells.
We express insect specific toxins in baculoviruses as green approaches to insect
pest control. Mammal specific toxins are used as probes to study the vertebrate
nervous system and potential pharmaceutical leads.
»Click image for larger version.
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Fisher
Lab. ATP sulfurylase catalyzes the adenylyl group transfer of ATP onto
inorganic sulfate to produce adenosine 5-phosphosulfate (APS). This is the first
step in the biological assimilation of inorganic sulfate. In fungi, ATP sulfurylase
is an oligomer composed of six identical subunits, and is allosterically regulated
by PAPS, the product of APS kinase. Shown here are the conformational changes seen
in the ATP sulfurylase hexamer upon binding the allosteric inhibitor PAPS, which
results in decreased enzyme activity.
»Click image for larger version.
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Wilson
Lab. Our lab studies the structure of proteins containing WD repeats, a
~40 amino acid motif found in approximately 1-2% of all eukaryotic proteins. Despite
the striking regularity and similarity of these propeller-like structures, they
function in very divergent cellular processes. Clockwise from the upper left, Bub3,
a mitotic checkpoint regulator; Ski8, a protein mediating nonstop mRNA degradation;
Aip1, a protein involved in actin depolymerization and Sif2, functioning in histone
deacetylation.
»Click image for larger version.
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Cheng
Lab. Alphavirus represents one of the best known model systems of macromolecular
assembly in the context of studying virus-cell interaction. The RNA genome (red)
is packaged into a nucleocapsid (orange for the capsid proteins), which is surrounded
by a lipid bilayer (green) with transmembrane spike proteins (blue). One of the
key questions is how the viral proteins drive the assembly reactions through the
cytoplasm (left), and how the nucleocapsids bud out from the cellular membrane in
forming a mature virion with lipid envelop, capable of further infections. Our research
interest is to determine the conformations of the virus and the cellular compartments
at the various stages of life cycle. This would help us to understand the mechanism
of virus functions as well as the design of anti-viral drugs more effectively.
»Click image for larger version.
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Kowalczykowski
Lab. The image is of a DNA catenane produced by RecQ helicase and DNA topoisomerase
III, in the presence of SSB protein. Atomic force microscopy was used to visualize
the DNA, which had been coated with RecA protein to enhance resolution and thereby
facilitate tracing of the path followed by the duplex DNA strands.
»Click image for larger version.
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