Not exact matches
Burke predicts
more fluorescent
proteins and dyes that indicate
cellular events (e.g., neurotransmission) will make real - time, rapid imaging appealing to many scientists.
For instance, Evan's blue, a dye that stains the
cellular protein albumin, penetrates the brain 10 times
more efficiently in stressed mice than in unstressed mice.
Because they act while embedded within the
cellular membrane, transmembrane
proteins have proven to be
more difficult to study than
proteins that operate in the watery solution that make up the cells» cytoplasm or in the extracellular fluid.
After
more than six years of research, the research team led by María Soengas, head of CNIO's Melanoma Group, showed that RAB7 acts as an orchestra director, determining the fate of melanoma cells: at high concentrations of RAB7,
cellular autodigestion is very active, and this allows tumor cells to obtain energy, prevent the accumulation of toxic components and thus divide and proliferate; when RAB7 is reduced, cells use endosomes to recycle metastatic
proteins, favouring their dispersal throughout the body.
Once considered nothing
more than a
cellular courier, RNA turns out to be astonishingly versatile, not only encoding genetic information but also acting like a
protein.
What's
more, only a very small percentage (6 %) of
proteins encoded by Pandoravirus salinus are similar to those already identified in other viruses or
cellular organisms.
The latter are
more easily accessible to the
cellular machinery that translates genes into their
protein products.
They found that by attaching to a mitochondrial
protein called TOM20, alpha - synuclein prevented the mitochondria from functioning optimally, which resulted in the production of less energy and
more damaging
cellular waste.
«Single enzyme's far - reaching influence in human biology, disease: Enzyme Fam20C chemically modifies
more than 100 different secreted
proteins, thus directing numerous
cellular processes.»
The researchers found that the
more aggressive the cancer, the higher the expression of this
protein, which helps maintain
cellular stability.
Previous studies in the lab showed that once HCMV is inside the cell, it quickly becomes latent by entering the cell's nucleus and co-opting a
cellular protein called Daxx — part of the intrinsic immune system — to shut down its own replication, the process of reproducing its genetic material to make
more copies of itself.
By fiddling with the
cellular postal codes that direct
proteins to the appropriate destination, they inserted a
more efficient mannosidase and engineered a yeast strain with glycoproteins containing far fewer mannose groups, they reported earlier this year.
«Since
protein synthesis is one of the most prominent hallmarks of
cellular life, it shows that these new viruses are
more «cell - like» than any virus anyone has ever seen before.»
A universal difference between
cellular genomes is that they are far larger and have far
more proteins called histones than viral genomes.
In this new paper, the researchers reveal
more about that mechanism, showing that without the protective ability of BRCA1, breaks in the DNA strands go unfixed, prompting the molecule ATM kinase to activate a
cellular «suicide» pathway involving a
protein called p53.
In the current paper, the shapes are made up of strut - reinforced tripods, which assemble themselves from individual DNA strands in a process called â $ œDNA origami.â $ Already, at 5 megadaltons, each tripod is
more massive than the largest known single
protein (titin, involved in muscle contraction) and
more massive than a ribosome, one of the
cellular factories in which
proteins are made.
For example, inflammation in brain tissue caused by either genetic susceptibility or triggered by accumulating
cellular proteins and external events, such as severe concussions, will leave the brain
more open to injury.
Autophagy (
more specifically macroautophagy) is the process by which
cellular compartments, such as membranes and organelles and also
protein aggregates, are recycled back into their building blocks [122].
Hartl, a biochemist, and Horwich, a geneticist, are pioneers in the realm of
cellular protein... Read
more
In these tools, NanoLuc - fluorescent
protein fusion shifts NLuc's bright blue luminescence to wavelenghts
more friendly for
cellular and in vivo imaging.
On their own, these unstable
proteins might be expected to perform their
cellular duties
more poorly, possibly causing harm to the organism.
Certain particle compounds may directly generate ROS in vivo because of their surface chemistry (eg, metals, organic compounds, and semiquinones) or after bioactivation by cytochrome P450 systems (eg, polycyclic aromatic hydrocarbon conversion to quinones).6, 290 a, 290 b A particle surface or anions present on otherwise
more inert particles may disrupt iron homeostasis in the lung and thereby also generate ROS via Fenton reactions.291 Other PM constituents may do so indirectly by the upregulation of endogenous
cellular sources (eg, nicotinamide adenine dinucleotide phosphate [NADPH]-RRB- oxidase) 292,293 or by perturbing organelle function (eg, mitochondria) by taken - up PM components.261 Particle stimulation of irritant and afferent ANS fibers may also play a role in local and systemic oxidative stress formation.294 Given the rich antioxidant defenses in the lung fluid, secondarily generated oxidization products of endogenous molecules (eg, oxidized phospholipids,
proteins) or a reduction in endogenous antioxidants per se may be responsible at least in part for the state of oxidative stress in the lungs (along with instigating the subsequent
cellular responses) rather than ROS derived directly from PM and its constituents.
Abundant
cellular glucose, caused by high blood glucose levels, enable them to reproduce and generate immune - impairing
proteins more prolifically.
Glycated
proteins and
cellular structures have altered function, increased vulnerability to oxidative damage, and reduced degradation and clearance.6 Slowing the entry of glucose into the brain would delay these processes and possibly give the body's defenses
more time to dispose of the AGEs.
As cells become
more insulin resistant, the pancreas faithfully cranks out even
more insulin, causing levels of C - reactive
protein to rise in the body — which triggers
cellular inflammation.
Large amounts of this
protein create a
cellular matrix, or a scaffolding, to which other structural
proteins attach themselves to reform the wound, including
more collagen itself.
The
more mitochondria we have, and the better they work, the better the
cellular infrastructure for cranking out new
proteins to GROW.
Well, it could be that the supplements are full of amino acids and phytonutrients that are amazing for the overall health of the body (which naturally improves the health of the skin) or it could be that the specific amino acids that the collagen
protein are utilized to produce
more collagen — again, the jury is still out at the
cellular level.