Thus, distribution and mobility of specific lipid species at the plasma membrane appears to precisely
regulated by membrane - associated proteins.
Not exact matches
Fermentation
by intestinal probiotics leads to enhanced production of short - chain fatty acids, including butyrate, which is a major energy source for the intestinal cell
membrane; propionate, which is involved in
regulating cholesterol; and acetate, which is involved in cholesterol synthesis.
It was commissioned
by Roderick MacKinnon, who shared the Nobel prize in 2003 for his work describing the structural and mechanistic properties of such channels, which are tunnels that
regulate the flow of ions across cellular
membranes.
The synaptic vesicle protein that mediates
membrane fusion during exocytosis also
regulates the rate and extent of this process
by controlling vesicle tethering.
«This is the first drug molecule that can
regulate memory loss
by directly blocking ions from leaking through nerve cell
membranes,» said Ratnesh Lal, a professor of bioengineering at the University of California San Diego and co-senior author of the study.
However, endocytic waves may be initiated
by clathrin through a positive feedback mechanism between clathrin and downstream proteins which includes actin
regulating proteins as well as
membrane proteins such as PIP3.
These cell activities are
regulated by proteins normally found at the cell's
membrane.
Eukaryotic cells are compartmentalized
by membranes, whose shape and dynamics are precisely
regulated to maintain their correct functions.
Arterial tone is
regulated in large part
by the influx of calcium through voltage-gated calcium (CaV channels, which are found in the
membranes of excitable cells throughout the body.
Voltage - dependent potassium ion (K +) channels (Kv channels) conduct K + ions across the cell
membrane in response to changes in the
membrane voltage, thereby
regulating neuronal excitability
by modulating the shape and frequency of action potentials.
OPTN may act
by regulating membrane trafficking and cellular morphogenesis via a complex that contains Rab8 and hungtingtin (HD).
The extracellular leaflet of the plasma
membrane is not characterized
by unique molecular targets but
by overexpressed antigens that are relatively down
regulated in healthy cells.
Dysferlin
regulates cell
membrane repair
by facilitating injury - triggered acid sphingomyelinase secretion.
Living cells are surrounded
by a
membrane that tightly
regulates what gets in and out of the cell.
Targeting of the FYVE domain to endosomal
membranes is
regulated by a histidine switch.
Bif - 1
regulates Atg9 trafficking
by mediating the fission of Golgi
membranes during autophagy.
The intrinsic pathway drives cell death
by permeabilization of the outer mitochondrial
membrane and is
regulated by the Bcl - 2 oncogene family of pro- and antiapoptotic factors.
Abbreviations: Aβ, amyloid β - peptide; AD, Alzheimer's disease; ALS, amyotrophic lateral sclerosis; Ambra1, activating molecule in Beclin -1-
regulated autophagy; AMPK, AMP - activated protein kinase; APP, amyloid precursor protein; AR, androgen receptor; Atg, autophagy - related; AV, autophagic vacuole; Bcl, B - cell lymphoma; BH3, Bcl - 2 homology 3; CaMKKβ, Ca2 + - dependent protein kinase kinase β; CHMP2B, charged multivesicular body protein 2B; CMA, chaperone - mediated autophagy; 2 ′ 5 ′ ddA, 2 ′, 5 ′ - dideoxyadenosine; deptor, DEP - domain containing mTOR - interacting protein; DRPLA, dentatorubral pallidoluysian atrophy; 4E - BP1, translation initiation factor 4E - binding protein - 1; Epac, exchange protein directly activated
by cAMP; ER, endoplasmic reticulum; ERK1 / 2, extracellular - signal -
regulated kinase 1/2; ESCRT, endosomal sorting complex required for transport; FAD, familial AD; FDA, U.S. Food and Drug Administration; FIP200, focal adhesion kinase family - interacting protein of 200 kDa; FoxO3, forkhead box O3; FTD, frontotemporal dementia; FTD3, FTD linked to chromosome 3; GAP, GTPase - activating protein; GR, guanidine retinoid; GSK3, glycogen synthase kinase 3; HD, Huntington's disease; hiPSC, human induced pluripotent stem cell; hVps, mammalian vacuolar protein sorting homologue; IKK, inhibitor of nuclear factor κB kinase; IMPase, inositol monophosphatase; IP3R, Ins (1,4,5) P3 receptor; I1R, imidazoline - 1 receptor; JNK1, c - Jun N - terminal kinase 1; LC3, light chain 3; LD, Lafora disease; L - NAME, NG - nitro - L - arginine methyl ester; LRRK2, leucine - rich repeat kinase 2; MIPS, myo - inositol -1-phosphate synthase; mLST8, mammalian lethal with SEC13 protein 8; MND, motor neuron disease; mTOR, mammalian target of rapamycin; mTORC, mTOR complex; MVB, multivesicular body; NAC, N - acetylcysteine; NBR1, neighbour of BRCA1 gene 1; NOS, nitric oxide synthase; p70S6K, ribosomal protein S6 kinase - 1; PD, Parkinson's disease; PDK1, phosphoinositide - dependent kinase 1; PE, phosphatidylethanolamine; PI3K, phosphoinositide 3 - kinase; PI3KC1a, class Ia PI3K; PI3KC3, class III PI3K; PI3KK, PI3K - related protein kinase; PINK1, PTEN - induced kinase 1; PKA, protein kinase A; PLC, phospholipase C; polyQ, polyglutamine; PS, presenilin; PTEN, phosphatase and tensin homologue deleted from chromosome 10; Rag, Ras - related GTP - binding protein; raptor, regulatory - associated protein of mTOR; Rheb, Ras homologue enriched in brain; rictor, rapamycin - insensitive companion of mTOR; SBMA, spinobulbar muscular atrophy; SCA, spinocerebellar ataxia; SLC, solute carrier; SMER, small - molecule enhancer of rapamycin; SMIR, small - molecule inhibitor of rapamycin; SNARE, N - ethylmaleimide - sensitive factor - attachment protein receptor; SOD1, copper / zinc superoxide dismutase 1; TFEB, transcription factor EB; TOR, target of rapamycin; TSC, tuberous sclerosis complex; ULK1, UNC -51-like kinase 1; UVRAG, UV irradiation resistance - associated gene; VAMP, vesicle - associated
membrane protein; v - ATPase, vacuolar H + - ATPase; Vps, vacuolar protein sorting
More recently, Drs. Goldstein and Brown discovered the SREBP family of
membrane - bound transcription factors and the elucidation of the proteolytic pathway
by which the SREBPs become activated to
regulate lipid metabolism.
Dietary fibre modifications that are low in fat and glucose reduce the risk for AD
by not only effecting cell
membranes and nutrient sensing G coupled receptors but also
by regulating number of nuclear receptors such as histone deacetylases (HDAC) and peroxisome proliferator activated receptors (PPAR) that control glucose, fatty acids and cholesterol and have significant effects on the brain cholesterol homeostasis and amyloidosis.