While working with Jung at Harvard, she identified a novel molecular mechanism through which
a protein in human cells called RIG - I mediates defense against viruses.
PLUMP PARTICLES Fats lurking in house dust can activate
a protein in human cells that researchers think plays a key role in obesity.
«By identifying this major regulator of noncoding editing in C. elegans we can now focus on dissecting the regulatory mechanism and determining the conservation of this regulatory
protein in human cells.»
This work raises the possibility that histones can signal to non-histone
proteins in human cells, and that deregulation of these events caused by MLL mutations might contribute to leukemia development.
[PRESS RELEASE 2017-05-05] A new study in Science from Karolinska Institutet maps out how different DNA - binding
proteins in human cells react to certain biochemical modifications of the DNA molecule.
Not exact matches
But
in the lab, when the scientists manipulated
human cells to be able to create the water bear shielding
protein — called Dsup — they showed about half the DNA damage as normal
cells.
For example, instead of using the
protein scissors to cut a virus, they can be used to cut out DNA
in a
human cell and replace it with DNA of the scientist's choosing.
Humans have roughly 20,000 to 25,000 genes, which encode
proteins that perform vital jobs
in our
cells.
Capsaicin only inflames
human cells because heat - detecting
proteins in our nerve endings called TRPV1 receptors become activated
in the chemical's presence, mistakenly interpreting capsaicin as a sign of extreme heat, and sending the body's burn defenses into overdrive.
Because the
human cells had been genetically engineered to express green fluorescent
protein, the tiny blobs showed up
in brilliant lime through the transparent window that the scientists glued into the mice's skull.
Then a team of Chinese researchers used that base editor to correct a mutation
in human embryos that causes the blood disorder beta - thalassemia, reported September 23
in Protein &
Cell (SN: 11/25/17, p. 7).
Sharon joined Anglister's lab for her master's project and Ph.D., studying the three - dimensional structure of a region
in the HIV - 1
protein envelope that helps the virus enter
human cells.
Hematopoietic stem
cells, that form mature blood
cells, require a very precise amount of
protein to function — and defective regulation of
protein production is common
in certain types of aggressive
human blood cancers.
Other researchers have tried changing
cell behavior by creating
protein switches from scratch, but Lim's approach — mixing and matching naturally existing
proteins — may be more versatile and practical: «It can be useful as a biotechnology device or for repairing
cells in humans.
Endocytosis of Frizzled 4 (Fz4)
in human embryonic kidney 293
cells was dependent on added Wnt5A
protein and was accomplished by the multifunctional adaptor
protein β - arrestin 2 (βarr2), which was recruited to Fz4 by binding to phosphorylated Dvl2.
In humans, Huntington's is an inherited disease caused by a gene encoding a toxic
protein, called mutant huntingtin, which causes brain
cells to die.
Strategies that boost the
cell's quality control programs, rather than disarm specific pathologic
proteins, have looked promising
in lab animals that serve as models for
human neurodegenerative disorders including Alzheimer's, Parkinson's, Huntington's, amyotrophic lateral sclerosis (ALS) and frontotemporal dementia.
Using
human fetal «mini-brains» grown
in 3 - D cultures, scientists determined that a specific
protein produced by the Zika virus changes the properties of neural stem
cells in the developing brain of an infected fetus, potentially causing microcephaly
in newborns (Ki - Jun Yoon, abstract 103.06, see attached summary).
But the London researchers have shown a few small changes
in the shape of a surface
protein were all it took to enable the bird version of Spanish flu to bind onto
human cells.
In experiments on zebrafish, Freiburg researchers have demonstrated that the same proteins that lead to the formation of metastases in humans also cause the cells to migrate during embryonic developmen
In experiments on zebrafish, Freiburg researchers have demonstrated that the same
proteins that lead to the formation of metastases
in humans also cause the cells to migrate during embryonic developmen
in humans also cause the
cells to migrate during embryonic development.
There are hundreds of RNA - binding
proteins in the
human genome that together regulate the processing, turnover and localization of the many thousands of RNA molecules expressed
in cells.
But Welte speculates that when internal temperatures do fluctuate
in humans, as
in the case of fevers, our
cells may also need a way to coordinate the
protein - building process.
Goats as Drug Factories Initially, GTC generated transgenic goats by microinjecting into the developing nucleus of a one -
cell embryo a gene encoding the desired
human protein (along with DNA that promotes activation of that gene
in milk).
«Artemisinin causes damage to the
proteins in the malaria parasite that kill the
human cell, but the parasite has developed a way to deal with that damage.
Human immunodeficiency virus - type 1 (HIV - 1) replicates actively
in infected individuals, yet
cells with intracellular depots of viral
protein are observed only infrequently.
By analyzing chemical changes of the IRS - 2
protein in immortalized cultures of
human white blood
cells, it determined that IRS - 2 appeared
in two different forms — «on,» which allows the signal to pass through, and «off,» which stops the signal from activating the
cells into M2 macrophages.
Professor Ali Tavassoli, who led the study with colleague Dr. Ishna Mistry, explains: «
In an effort to better understand the role of HIF - 1 in cancer, and to demonstrate the potential for inhibiting this protein in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
In an effort to better understand the role of HIF - 1
in cancer, and to demonstrate the potential for inhibiting this protein in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
in cancer, and to demonstrate the potential for inhibiting this
protein in cancer therapy, we engineered a human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed in a hypoxic environmen
in cancer therapy, we engineered a
human cell line with an additional genetic circuit that produces the HIF - 1 inhibiting molecule when placed
in a hypoxic environmen
in a hypoxic environment.
The researchers observed the effect of the synthetically produced molecule, JK - 31, on the growth and proliferation of a model
human breast cancer
cell line and found that it effectively blocked the
protein cyclin - dependent kinase 1 (CDK1), which plays a key part
in the process of the division of cancer
cells, and therefore inhibited the proliferation of the
cells.
In the
human body
cells turn genes on and off by means of chemical modifications that change DNA and related
proteins.
Lambs produced from the genetically manipulated
cells produce foreign
proteins; such animals may be able to manufacture large quantities of medically valuable
human proteins in their milk.
Meanwhile, a
protein commonly found
in the blood of young mice (and
humans) may hold the key to rejuvenating brain
cells.
Scientists have a better way to study
human proteins — large molecules that are part of every
cell in the body — thanks to a new technology developed by University of Toronto researchers.
«Most previous research into ways of delaying the onset of HD symptoms have focused on studying the mutant
protein in cells or
in animal models, but the relevance of abnormalities
in those systems to what actually happens
in patients remains a huge assumption,» says James Gusella, PhD, director of the Center for
Human Genetic Research (CHGR) at Massachusetts General Hospital (MGH), corresponding author of the
Cell paper.
Now, scientists have a provocative new theory that might explain
in part this universal
human decline: Dying
cells secrete a
protein that could trigger others to die as well, accelerating the body's deterioration.
«This technology gives us a new tool to examine membrane
proteins in their natural environment of the
human cell,» said Igor Stagljar, a Professor
in the Donnelly Centre for Cellular and Biomolecular Research.
Their major hurdle: to come up with a replacement for hemoglobin (an iron - enriched
protein in red blood
cells that transports oxygen from the lungs to the rest of the body) that can be directly introduced into the
human circulatory system.
Follow - up tests
in human cell cultures confirmed that MIR168a interferes with production of a cholesterol - clearing
protein.
The result, published January 5
in Science Immunology, suggests that the
protein, a receptor involved
in immune
cell signaling, plays a role
in spontaneous abortions and other
human pregnancy complications.
«
In our
human airway epithelial model system, one of the drugs destabilizes and deactivates the
protein that the other drug tries to correct,» said Martina Gentzsch, PhD, an assistant professor of
cell biology and physiology and senior author of the UNC Science Translational Medicine paper.
SIX3 and a related gene, SIX2, with a similar pattern of expression
in human beta
cells, encode
proteins known as transcription factors that control the expression of many other genes
in the
cell.
First, the destabilizing effects of VX - 770 on the corrected CFTR
protein might be less robust
in the
human body than were the effects seen
in lab tests using
human lung
cells.
In all, scientists estimate that the human body contains about 100,000 different proteins, each the result of millions of years of evolutionary shuffling, culminating in a precise lineup of pleats, coils, and furrows required to carry out a specific job in the cel
In all, scientists estimate that the
human body contains about 100,000 different
proteins, each the result of millions of years of evolutionary shuffling, culminating
in a precise lineup of pleats, coils, and furrows required to carry out a specific job in the cel
in a precise lineup of pleats, coils, and furrows required to carry out a specific job
in the cel
in the
cell.
Working with
human breast cancer
cells and mouse models of breast cancer, scientists identified a new
protein that plays a key role
in reprogramming cancer
cells to migrate and invade other organs.
With more than 800 members
in the
human genome, GPCRs are the largest family of
proteins involved
in decoding signals as they come into the
cell and then adapt the
cell's function
in response.
In the past decade, scientists have watched protein and RNA molecules condensing into droplets, or membrane - free condensates, in many kinds of cells, from bacterial to huma
In the past decade, scientists have watched
protein and RNA molecules condensing into droplets, or membrane - free condensates,
in many kinds of cells, from bacterial to huma
in many kinds of
cells, from bacterial to
human.
Prof Robin Lovell Badge, Crick Institute, on the science: «The experiments reported by Junjiu Huang and colleagues (Liang et al)
in the journal
Protein Cell on gene editing
in abnormally fertilised
human embryos are, I expect, the first of several that we will see this year.
The DNA
in human cells is translated into a multitude of
proteins required for a
cell to function.
Specifically, the study — reported online
in The Journal of Infectious Diseases — shows that E. coli K1 modulates the
protein peroxisome proliferator - activated receptor - gamma (PPAR - γ) and glucose transporter - 1 (GLUT - 1) levels at the blood - brain barrier
in human brain microvascular endothelial
cells.
The researchers, who report their work
in the 26 October issue of Molecular
Cell, hope to soon create an altered version of the
protein that will work
in humans.
Losing a genetic switch that increases production of a
protein called GDF6 may have created the big toe and helped shape the
human foot for bipedalism, scientists propose
in a paper published online January 7
in Cell.