Matrix protein 2 of influenza a virus contagious,zyzz workout supplements gnc,injecting testosterone base,buy growth hormone booster - PDF Review

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This protein forms a continuous shell on the inner side of the lipid bilayer in virion, where it binds the ribonucleocapsids. Viren infizieren einen Wirtsorganismus, um seinen Stoffwechsel fur ihre eigene Vermehrung zu benutzen.
In bezug auf Viren kann man das gleichsetzen mit der DNA, allerdings nur in den Fallen, wo die Viren auch tatsachlich DNA enthalten.
Wurde je erforscht, ob Viren nicht nur Krankmacher sind, sondern auch genetische Informationen zwischen Lebewesen austauschen konnen? RNA packaged inside the togavirus capsid; note that the capsid is fenestrated (it has 'windows'). The nucleocapsid is partially covered by a coat of C protein and enveloped by a phospholipid bilayer viral membrane )derived from the host cell's membrane) which contains the viral protein spikes.Adhesion and Injection of DNAThe protein spikes adhere to specific receptors on the target cell surface-membrane. ViroidsViroids are plant pathogens that consist of circular ssRNA of about 300b (220 to 380 bases, the smallest is 220b). Subviral SatellitesHepatitis D virus (HDV) is the smallest known animal virus and has as mall genome of circular single-stranded RNA or (-)sscRNA of 1.7 kb, in which about 70% of the nucleotides pair with other bases in the molecule, forming a rod-like molecule. InfluenzaInfluenza virus is a (-)ssRNA virus whose genome is divided into 8 separate chromosomes (unusual for a virus!). The third type of projection, the short proteins (unshaded rods) that are not labelled in this diagram, and which project from between the M1 protein (unshaded circles) capsid, are M2 ions channels.
Function of the HA spikesThe haemagluttinin is involved in cell binding and each strain of influenza has one of 16 subtypes of H (designated H1 to H16).
The nucleocapsid, with its C protein shell enters the host cytosol and the RNA is released and escapes from the capsid.ReplicationThe replication of the RNA and the protein capsid and their packaging are summarised in the diagram below. This is translated from the second START codon, producing a different polyprotein which is cleaved to produce the late proteins which form the virus particle, and include the C protein. This virus is not able to complete its life-cycle without a helper virus, in this case hepatitis B virus (HBV). Influenza B, which infects humans, has a genome size of 14.648 kb and forms particles which are spherical to filamentous). The single-stranded RNA is a plus or positive-strand, meaning that it is of the right sense to be immediately transcribed directly into mRNA. In the meantime, the (-)-RNA is copied repeatedly to produce lots of (+)-strand RNA genomes which are packaged into the assembling virions. HDV must coinfect the same cell as HBV in order to complete its development as it requires some of the HBV genes. These 8 RNA segments are packaged into 8 helical ribonucleoprotein particles (RNPs) enclosed in a protein capsid (made of the matrix or M1 protein) surrounded by a phospholipid bilayer envelope (with the M protein lining the inside of the envelope). Three identical copies of the haemagluttinin polypeptide form a single haemagluttinin spike (it is trimeric, specifically a homotrimer).HA binds sialic acid-containing receptors on the target cell surface membrane. HIV has two (+)ssRNA molecules in its genome, represented above as the spirals (red) in the centre of the elongated inner core (yellow) which are both identical copies of the genome wound with packaging proteins to form ribonucleoprotein.


The model above is a togavirus (such as Semliki Forest Virus (SFV) or Sindbis virus).The core of the virus is the nucleocapsid - single-stranded RNA (ssRNA) packaged inside a protein capsid with icosahedral symmetry (not an icosahedron, in this instance as there are more than 20 triangular faces, but the symmetry is icosahedral). They code for no proteins and have no protein capsid or protein-coat at all: they are naked infectious RNA molecules and thus one of the simplest parasites conceivable.
A virus like HDV is called a satellite virus (or subviral satellite) and is thus parasitic on HBV. Embedded in the envelope are two types of glycoprotein spike: haemagluttinin (HA or H) so-called because it will cause red blood cells to stick together, and neuraminidase (NA or N). The elongated conical core shell (the shape of which is characteristic of the lentivirus variety of retrovirus, the core being icosahedral in some retroviruses).
Spike proteins are manufactured by the rough endoplasmic reticulum and Golgi apparatus of teh host cell before being added to the host cell-surface membrane, where they form patches (excluding host proteins) to which the assembled virions add and bud from the cell, acquiring their envelope as they do so. Their replication requires RNA polymerase II, provided by the host cell and occurs by rolling circle replication.
Sialic acid is a component of carbohydrate chains borne on the cell surface (the glycocalyx) and also of mucus (mucoproteins).The virus then tricks the target cell to take it up (by activating the receptor upon binding to it) and it is taken-up by (coated-pit) endocytosis into a vesicle called a coated vesicle. HIV is enveloped, that is it is enclosed in a phospholipid bilayer membrane (cyan) derived from the host cell-surface membrane. This is the fastest known self-cleaving ribozyme in nature, cutting the RNA in less than one second.
Some are ribozymes, meaning that they fold to form structures with enzymatic activity, such as catalysis of cutting the concatemers (produced by rolling circle replication) into individual viroids. Just beneath the envelope is a protein shell 9inner shell or matrix) which stabilises the structure of the envelope.HIV is well-known as the causative agent of AIDs (Acquired-immunodeficiency syndrome or acquired immune-deficiency syndrome) in which destruction of key components of the body's immune system leaves it very susceptible to many other infections. This occurs because HIV targets certain immune cells, especially T-helper cells (cells that act as alarms and 'officers' for the immune system - activating and directing other immune cells).
When the pH drops below 6, the HA changes shape, partially unfolding, which exposes a hydrophobic region (hydrophobic literally means 'water-fearing' and refers to substances that prefer to dissolve in lipids, rather than water) which attaches to the endosome membrane, like a grappling hook, then the HA stabilises and refolds, retracting as it does so and bringing the viral membrane so close to the endosomal membrane that the two membranes fuse.Function of the N spikesThe neuraminidase is a sialidase, an enzyme which cuts sialic acid residues from the ends of carbohydrate chains.
HIV will target these cells, enter them and turn them into virus factories!Retrovirus Cycle - example HIV1.
This breaks-up the long carbohydrate chains that form the slimey lining of respiratory airways and makes the mucus of the respiratory tract more watery, which helps the virus move easily to its target cells (one of the functions of mucus is to entangle foreign particles, such as viruses, and the N spikes counter this by cutting the entangling threads). These receptors are more-or-less specific, since viruses infect only one or a few cell types. The N spikes will also cleave sialic acid residues to which HA binds, if the target is inappropriate (such as a mucoprotein in the mucus layer rather than the cell receptor).There are also several types of N and the H and N types carried by a particular strain charcterise the virus. In the case of HIV, the gp120 spikes bind to CD4 receptors on T-cells (HIV can also infect a few other cell types, such as macrophages).
They import protons and are involved in triggering uncoating - the disassembly of the protein capsid which allows the RNPs to enter the host cytosol.Function of the three polymerase peptidesOnce in the cytosol the nucleoprotein which packages the RNA of each RNP, allows movement of the RNPs into the host cell nucleus. This is followed by a secondary and more stable adhesion between the vrius and a second receptor on the cell surface (CCR5 or CXCR4).


Once inside the nucleus, the three polymerase units (PA, PB1 and PB2) initiate transcription of the viral RNA. Once stably bound or adsorbed, the lipid envelope of the virus fuses with the host cell membrane (this fusion is triggered by gp41).
PB2 attaches to the cap present at the head end (5') of host mRNA, PB1 then cleaves this cap which attaches to PB2 - the virus steals the 5'-cap off host RNA to make itself look like mRNA! PB1 also adds the usual 3' tail to the end of the viral RNA, so now it resembles host mRNA ready to be transcribed! RNPs are assembled in the host cell nucleus and are then exported to the cytoplasm.M protein, HA and N accumulate together in the host cell-surface membrane (after being processed and delivered there by the rough endoplasmic reticulum and Golgi apparatus of the host cell). To complete this unusual task, of synthesising dsDNA from a ssRNA template, HIV carries the viral enzyme reverse transcriptase (RT) - blue spheres inside inner core in the diagram above. Note that as this step proceeds efficient gene expression, the virus must carry integrase, RNase and reverse transcriptase with it.
All these enzymes are represented by the blue spheres inside the viral core.HIV is unusual in that it can insert its provirus and replicate inside non-dividing cells. It does this with the help of at least two viral proteins: MA, which apparently acts as a key granting access past the NPC and Vpr. Transcription and expression of viral genesThe synthesis of virus proteins only begins efficiently once the provirus is integrated into the host DNA.
Some 95% of the time, Gap is produced, but 5% of the time, the ribosome shifts frame (due to a signal carried on the Gag mRNA and so misses the Gag STOP codon and continues onto pol which is encoded on the same mRNA, producing Gag-Pol.
A viral protease (Pro) then cleaves the Gag from the Pol and cuts up the Pol polypeptide into RT (reverse transcriptase, p50), In (integrase, p31), Pro (protease) and RNase H (p15, 50% of which remains linked to RT). About 20 Gag are produced to every Gag-Pol.Env - envelope glycoprotein -Env is sent to the host cell's Golgi apparatus where carbohydrate chains are added to it (glycosylation) to convert it into a glycoprotein (gp). The virus then buds from the host cell, acquiring the lipid envelope and then completes its maturation.Evading the host's immune systemHIV has several tricks for evading the defences of its host.
Antibodies produced by the host can, for example, bind to gp120 and prevent new viruses from infecting cells. In particular, gp120 contains five hypervariable regions, that is regions whose amino acid sequence and structure differ greatly between one HIV strain and another. The HIV polymerase (RT + RNase H) also lacks a proof-reading function - it does not check for errors and so it makes mistakes fairly frequently, causing HIV to mutate extremely rapidly, again increasing variation.
By rapidly varying its antigens, HIV can stay one step ahead of the immune system, changing to a new form once antibodies are developed, making those antibodies redundant.
This helps to explain why antibodies indicate HIV infection and the possibility of developing full-blown AIDS - the function of the antibodies is impaired!



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