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.
This changes a lot of what scientists thought they knew about how water bears deal with radiation,
as they were previously thought to have
proteins that repaired
damaged DNA, rather than
proteins that halt
damage altogether.
That's because the body is breaking down old,
damaged proteins and building new ones, which is a process called
protein breakdown and
protein synthesis, known collectively
as protein turnover.
It must be noted, however, that there are injurious grain
proteins that cause
damage and produce symptoms by mechanisms that are
as yet obscure.
As for the microwaves
damaging your food, it does so no more than any other cooking method (all heating of food will
damage proteins and enzymes, but your stomach does the same thing!
Joseph Mercola's new book «Fat For Fuel» has extremely good information on the importance of keeping a tight control on
protein (
as well
as carbs) because of the
damage they can cause to mitochondria — in fact he steers clear of almonds for that reason.
The reality is not «gentle
proteins», cute pink hearts or «probiotics just like those in breastmilk» but dirty contaminated bottles, diarrhea, babies screaming with pain from otitis media, babies separated from their mothers in pediatric wards with acute respiratory disease,
damaged guts that morph into chronic lifelong conditions such
as Crohn's disease, more women dying of breast cancer, the cost and pain of living a life with diabetes and lives cut short because of cardiac disease and so on.
The latter ties overproduction of free radicals to oxidative
damage to lipids,
proteins, and DNA, leading to chronic diseases such
as atherosclerosis, cancer, diabetes, and rheumatoid arthritis.
Other
proteins such
as histones are involved in the packaging of DNA or repairing the
damage to DNA that causes mutations.
Among those are
proteins that contribute to the production of seeds,
as well
as proteins involved in defending cells from heavy metal and radiation
damage.
One is that the cancer - related
proteins used by the test reflect tissue
damage and can also appear in people with inflammatory diseases such
as arthritis.
In a report on their study, published June 20
as an Early View article online in Annals of Neurology, the Johns Hopkins team found that increasing levels of the
protein clumps corresponded with worsening nerve
damage, indicating that the smaller skin biopsies they used appear to work well
as a measure of disease severity.
A common feature of neurodegenerative diseases such
as Alzheimer's, Parkinson's or Huntington's disease are deposits of aggregated
proteins in the patient's cells that cause
damage to cellular functions.
Current research is looking at why inhibiting certain molecules, such
as mouse
protein Stat3, promote muscle regeneration in mice and how to engineer orthopedic implants from stem cells to replace
damaged cartilage and bone, but the results of that effort aren't expected to be necessarily aimed at the old.
An earlier study indicated that the intermediate step was likely a floppy loop area formed by
proteins, which didn't seem compatible with the tough,
damaging fibril
as an end result.
Arising from the abnormal buildup of a
protein known
as alpha - synuclein in the brain, such conditions
damage the nerves that control blood pressure and heart rate.
Autophagy is also used for self - cleaning to eliminate other
proteins as well
as damaged or unneeded cellular components.
Generally,
as an organism ages, not only are there more
damaged proteins in need of disposal, but the proteasome itself becomes
damaged and less efficient in clearing out the
damaged proteins.
The
protein itself has been known to researchers for some time
as a result of research on zebrafish, where it plays an important role in the healing process following
damage to the spinal cord.
This study, published recently in PLOS Genetics, shows that in the particular case of meiotic cells such
as spermatocytes, the signalling route of the ATM
protein also participates in the control system of the cell cycle progression in response to DNA
damage, something which until now was unknown.
BRCA1 and 2, genes whose
proteins are supposed to work
as tumor suppressors and also repair DNA
damage, were the first known risk factor genes for familial breast cancer
as well
as ovarian and other cancers.
As researchers develop drugs that target the DUX4
protein, the hope is that these mice will be used to determine whether such drugs can reach skeletal muscle and allow muscle
damage to be repaired, even in the presence of DUX4.
In aging, this gene expression presumably occurs to compensate for the accumulation of
protein damages; during diapause, the same genes may be activated to prepare the whole embryo to catch up with the interrupted development and be ready to hatch
as the rainy season starts.
As study director Brack - Werner explained: «Several viral
proteins are toxic to neurons and may cause immune
damage in the brain.
Since Lipton's group co-discovered the SNO reaction some 20 years ago, scientists have linked the reaction to
protein misfolding and nerve cell
damage in cases of Alzheimer's, Huntington's, amyotrophic lateral sclerosis (ALS / Lou Gehrig's disease) and Parkinson's disease,
as well
as heart / cardiovascular disease and cancer.
Misshapen
proteins become entangled with neurons in prion diseases such
as Creutzfeldt - Jakob disease,
damaging or killing cells.
Just
as oxygen can rust iron that makes up a horseshoe or frying pan, it can
damage the iron - and - sulfur
proteins of the photosynthetic apparatus.
RIPK1, the researchers found, inflicts
damage by directly attacking the body's myelin production plants — nerve cells known
as oligodendrocytes, which secrete the soft substance, rich in fat and
protein that wraps around axons to support their function and shield them from
damage.
As expected, the antioxidants did reduce
damage to DNA but also reduced levels of p53, an essential
protein that suppresses...
That's good for probing delicate samples, such
as proteins, than can be
damaged by high - intensity light.
In research published in Molecular Cell, Rutgers scientists discovered that a
protein (p62), which is supposed to act
as an antioxidant to prevent cell
damage, was not working efficiently in laboratory mice with liver and heart disease that mimicked these conditions in humans.
CD74 is broken into products that fit into the groove of cell surface immune response
proteins as part of the chain of events that activates T cells — immune cells that normally attack infected (or
damaged) cells in the body.
Inside these cells is a
protein called alpha - synuclein, which is known to go awry and lead to
damaging clumps in the brains of Parkinson's patients,
as well
as those with Alzheimer's disease.
In 2011, UT Southwestern researchers in Dr. Levine's laboratory identified the
protein Smurf1
as important for the elimination of viruses and
damaged mitochondria from cells via a cellular housekeeping process called autophagy.
This could be one of the mechanisms responsible for the reduced regeneration capacity in the aged brain
as stem cells that retain larger amounts of
damaged proteins require longer for the next cell division.
The researchers were able to model the characteristics of A-T in the laboratory, such
as the cell's lack of ATM
protein and inability to repair DNA
damage.
When such DNA
damage occurs,
proteins known
as PARPs move to the site of
damage and begin to mend these broken strands of DNA, allowing cancerous cells and tumors to recover, grow and proliferate, thereby escaping the effects of treatment.
But over the years,
as damaged proteins accumulate in the lens, these chaperones become overwhelmed.
But until he understands how the cells are stressed in the first place, he won't know much: «We frankly don't have a clue
as to how much microwave radiation is needed to cause irreversible
damage to cellular
proteins.
Johns Hopkins University biologists have found that a
protein that plays a key role in the lives of stem cells can bolster the growth of
damaged muscle tissue, a step that could potentially contribute to treatments for muscle degeneration caused by old age and diseases such
as muscular dystrophy.
He then explains how x-rays from NSLS - II can provide new capabilities to study
proteins —
as they jiggle and wiggle — to learn more about them, including their remarkable roles in repairing
damaged DNA.
As luck would have it, cells in the brain called microglia act as the brain's street sweeper, zapping infectious agents, damaged cells, and, importantly, protein tangles and plaques that are thought to cause dementi
As luck would have it, cells in the brain called microglia act
as the brain's street sweeper, zapping infectious agents, damaged cells, and, importantly, protein tangles and plaques that are thought to cause dementi
as the brain's street sweeper, zapping infectious agents,
damaged cells, and, importantly,
protein tangles and plaques that are thought to cause dementia.
At the same time, when mice that lacked the RGS6
protein were treated chronically with alcohol, they experienced less
damage to heart and liver
as well
as the lining of the gut compared to mice with the
protein.
As the DNA replication process unzips the DNA and becomes blocked by DNA
damage, sometimes a motor
protein recognizes the stall.
When this vasculature — the blood - brain barrier (BBB)-- ruptures, blood
proteins can enter into the brain and cause edema and neuronal
damage in a variety of neurological diseases, such
as stroke, multiple sclerosis, Alzheimer's disease, and spinal cord injury.
The
protein p53 is a key activator of the cell's protective machinery against genetic
damage, such
as the mutations that drive cancer cells» explosive growth.
A large variety of methods is used including genetic, molecular and cytogenetic techniques, fluorescence in situ hybridisation and DNA «combing»,
as well
as high throughput sequencing approaches such
as DNA - seq for mutation landscape analyses, RNA - seq for transcriptome analyses and ChIP - seq mapping of chromatin - associated
proteins and their genome - wide modulation in response to DNA
damages.
Bradshaw PS, Stavropoulos DJ, Meyn MS. Human telomeric
protein TRF2 associates with genomic double - strand breaks
as an early response to DNA
damage.
Persistent DNA
damage and DDR signaling triggers senescent cells to secrete immunomodulatory
proteins, a phenomenon known
as the senescence - associated secretory phenotype (SASP).
The
proteins and other constituents of our cells are all eventually
damaged as the result of biochemical accidents that occur during normal metabolism, or simply outlive their usefulness.