Publication Date:
2024-03-28
Description:
This reprint presents recent developments in the field of biological liquid–liquid phase separation (LLPS, also known as biomolecular condensation). LLPS and related biogenesis of various membraneless organelles (MLOs) and biomolecular condensates (BMCs) represent fundamental molecular mechanisms governing the spatio-temporal organization of the intracellular space. In fact, MLOs and BMCs, being liquid droplets, represent specific compartments within a cell that are not enclosed by a lipid membrane. Most biological LLPS processes are reversible, and many MLOs/BMCs exist transiently; they rapidly emerge when conditions are changed and rapidly disintegrate as soon as the original conditions are restored, thereby showing a characteristic “now you see me, now you don’t” behavior. Numerous MLOs/BMCs are found inside eukaryotic cells, where they exist as liquid droplets (or cellular bodies, puncta, etc.) in the cytoplasm, nucleoplasm, mitochondrial matrix, and stroma of chloroplasts. Furthermore, MLOs/BMCs are commonly observed in Archaea, bacteria, and, likely, viruses. MLOs/BMCs have numerous crucial functions, and their biogenesis is known to be controlled by various external factors and environmental cues, such as changes in temperature, pH, and ionic strength of the solution. All of these have garnered the close attention of many researchers to biological LLPS, MLOs, and BMCs.
Keywords:
Alzheimer’s disease
;
amyloid aggregation
;
lipid bilayer
;
cholesterol
;
time-lapse AFM imaging
;
molecular dynamics
;
liquid–liquid phase separation (LLPS)
;
membraneless organelles
;
phase-separated condensates
;
human diseases
;
liquid–liquid phase separation
;
intrinsically disordered proteins
;
proteins with low complexity
;
P-body
;
Nst1
;
polyampholyte domain
;
aggregation-prone domain
;
Saccharomyces cerevisiae
;
membrane-less organelle
;
nuclear speckle
;
nucleolus
;
phase separation
;
chromatin organization
;
nuclear condensate
;
intrinsically disordered region
;
transcription
;
DNA damage repair
;
super-enhancer
;
quantitative imaging
;
CTP synthase
;
cytoophidium
;
fluorescence recovery after photobleaching (FRAP)
;
stimulated emission depletion (STED)
;
Drosophila
;
epithelium
;
follicle cell
;
ingression
;
paramyxoviruses
;
Hendra virus
;
amyloid-like fibrils
;
Taylor Dispersion Analysis (TDA)
;
negative staining Transmission Electron Microscopy (ns-TEM)
;
Polyethylene glycol (PEG) precipitation assays
;
Congo Red
;
Small-Angle X-ray Scattering (SAXS)
;
actin
;
actin polymerization
;
actin-binding proteins
;
coacervate
;
membrane
;
signaling proteins
;
n/a
;
thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
;
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
Language:
English
Format:
application/octet-stream
