extracellular parasitism - definição. O que é extracellular parasitism. Significado, conceito
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O que (quem) é extracellular parasitism - definição

Extracellular domain

Parasitism (social offense)         
  • hard labor]] in [[Arkhangelsk Oblast]] for "social parasitism". In 1987 he won the [[Nobel Prize in Literature]].
PEJORATIVE THAT IS LEVELED AGAINST A GROUP OR CLASS WHICH IS CONSIDERED TO BE DETRIMENTAL TO SOCIETY
Parasitism (social offense)
Social parasitism was a political crime in the Soviet Union in which the perpetrator was accused of living at the expense of other people or society. A number of Soviet intellectuals and dissidents were accused of the crime of parasitism, including Joseph Brodsky, Iosif Begun, Vladimir Voinovich, Lev Kopelev and Andrei Amalrik.
Extracellular vesicle         
VESICLE THAT IS PART OF THE EXTRACELLULAR REGION
Extracellular vesicles; Apoptotic body
Extracellular vesicles (EVs) are lipid bilayer-delimited particles that are naturally released from almost all types of cell and, unlike a cell, cannot replicate. EVs range in diameter from near the size of the smallest physically possible unilamellar liposome (around 20-30 nanometers) to as large as 10 microns or more, although the vast majority of EVs are smaller than 200 nm.
Extracellular polymeric substance         
  • Extracellular polymeric substance matrix formation in a [[biofilm]]
  • Sinorhizobium meliloti]]''
GLUEY POLYMERS SECRETED BY MICROORGANISMS TO FORM BIOFILMS
Extracellular polymeric substances; Exopolysaccharide; Exopolysaccharides; Extracellular polysaccharide
Extracellular polymeric substances (EPSs) are natural polymers of high molecular weight secreted by microorganisms into their environment. EPSs establish the functional and structural integrity of biofilms, and are considered the fundamental component that determines the physicochemical properties of a biofilm.

Wikipédia

Ectodomain

An ectodomain is the domain of a membrane protein that extends into the extracellular space (the space outside a cell). Ectodomains are usually the parts of proteins that initiate contact with surfaces, which leads to signal transduction. A notable example of an ectodomain is the S protein, commonly known as the spike protein, of the viral particle responsible for the COVID-19 pandemic. The ectodomain region of the spike protein (S) is essential for attachment and eventual entry of the viral protein into the host cell.

Ectodomains play a crucial part in the signaling pathways of viruses. Recent findings have indicated that certain antibodies including the anti-receptor binding domain (anti-RBD) or anti-spike ectodomain (anti-ECD) IgG titers can act as virus neutralization titers (VN titers) which can be identified in individuals with diseases, dyspnea and hospitalizations. In perspective of severe acute respiratory syndrome corona virus 2 (SARS-Cov-2) these specific ectodomains may detect antibody efficacy against SARS-Cov-2, in which VN titers can classify eligible plasma donors. Protective measures against diseases and respiratory conditions can further be advanced through ongoing research on ectodomains. Ectodomain's play a crucial part in the signaling pathways of viruses. In perspective of severe acute respiratory syndrome corona virus 2 (SARS-Cov-2) these specific ectodomains may detect antibody efficacy against SARS-Cov-2, in which VN titers can classify eligible plasma donors. Protective measures against diseases and respiratory conditions can further be advanced through ongoing research on ectodomains.

Ectodomains also interact with membrane systems inducing vesicle aggregation, lipid mixing and liposome leakage which provides information as to how certain viruses spread infection throughout the cellular domain. Specifically, the hepatitis C virus (HCV) utilize a fusion process in which the ectodomain of HCV E2 envelope protein confers fusogenic properties to membrane systems implying HCV infection proceeds throughout the cell through receptor mediated endocytosis. These findings in the role of the ectodomains interacting with target membranes give insight into virus destabilization and mechanism of the fusion of viral and cellular membrane which is yet to be further characterized.