Virology: Chapter 3 Flashcards

(40 cards)

1
Q

where is the location of protein assembly

A

cytoplasm / nucleus
(some start in the nucleus and complete it in the cytoplasm)

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2
Q

all components of virus particles must accumulate in …

A

1 location

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3
Q

proteins must ….. with viral genome in order to be packaged

A

bind

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4
Q

proteins have affinity for viral nucleic acids, this means…

A

they can interact with nucleic acids

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5
Q

what is the trigger of assembly

A

when high concentration of viral genome + proteins accumulate exceeding a threshold
(they have high affinity)

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6
Q

when does protein assembly happen

A

after genome replication

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7
Q

assembly requires energy yes or no

A

yes it’s energetically favourable

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8
Q

capsid is made out of subunits that spontaneously assemble, what are the 3 interactions?

A

folding into secondary / tertiary structures
hydrogen bonds
hydrophobic interactions

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9
Q

what is the difference between simple and complex assembly

A

simple: only rely on capsin protein interactions and it’s affinity

complex: multi-step process that involves structural, non-structural and cellular proteins

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10
Q

genome packaging in the capsid can be done both either early or later on

A

yes, true

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11
Q

Helical capsid assembly

A

self-assemble around the genome (in cytoplasm)

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12
Q

Icosahedral capsids

A

assemble by affinity around the genome (in cytoplasm)

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13
Q

Complex capsids

A

use scaffolding proteins forming empty procapsids then genome is added after those proteins are removed (in cytoplasm)

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14
Q

Assembly in the Nucleus (Nuclear Assembly), is usually for some DNA viruses, where their capsid proteins need….

A

nuclear localization signals

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15
Q

for assembly in the nucleus, large icosahedral capsids need what protein

A

scaffolding protein

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16
Q

Why are capsids made using subunit construction?

A
  • use less genetic material since it’s a repeating unit.
    if you use 1 large protein, it might not cover the entire genome
    misfolding proteins is common so using subunits, we can avoid that
  • subunits are more stable
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17
Q

2 types of virus egress

A

cell lysis and budding

18
Q

cell lysis is only for…

A

naked virus / non-enveloped

19
Q

budding is only for…

A

enveloped virus

20
Q

process of cell lysis

A

cell breaks open, release virus, kills host cell, due to viruses release viroporins / lytic phospholipids to disrupt membrane

21
Q

why does budding not harm the cell?

A

because it maintains the integrity of the plasma membrane

22
Q

process of cell budding (starting with virus is fully assembled)

A

virus move towards host membrane
viral proteins trigger membrane to curve around virus particle
virus wraps itself in the curve membrane so it becomes the virus envelope
scission: membrane “pinches off” and virus released

23
Q

Why enveloped viruses bud?

A

because they need to have a membrane envelope to infect the next cell

24
Q

what is the function of the envelope

A

hide from the immune system and carries spike proteins so virus can attach to receptor

25
Using eukaryotic cells as a host cell can have its limitations, one of which is the cell's DNA and RNA pol are in the nucleus, explain why is that a disadvantage towards RNA viruses that replicate in the cytoplasm
they can't use the DNA / RNA pol because its in the nucleus, so they bring their own enzymes, RDRP
26
another disadvantage is that eukaryotic cells lack enzymes that synthesize viral mRNA from viral RNA, so what does the virus have to do
bring it's own enzyme
27
viral mRNA don't have 5' cap or poly-3'-A tail like eukaryotic cell, why is that a limitation
the viral mRNA must out-compete the host mRNA for ribosomes to translate, or they must block host translation
28
eukaryotic ribosomes only translate one gene per mRNA (monocistronic), why is that a limitation for virus
this means virus must make an mRNA for each gene OR make mRNA for all genes that can be translated into one polyprotein, then it will be cleaved into multiple proteins
29
virus classification has 2 systems, which are..
classical system and baltimore system
30
in the classical system, viruses are group into genera based on their
shared properties NOT diseases / properties of the cell they infect
31
what are the 4 main properties of the classical system
1. Is Genome DNA/RNA? 2. Capsid Symmetry 3. Is there an envelope? 4. Dimension of virion + capsid
32
Baltimore system is based on the genetic system of each virus, it describes the relationship between...
genome and the production of the virus mRNA
33
what are the 3 main properties of the Baltimore system
1. Is Genome DNA/RNA 2. Is it (+) or (-) Sense 3. Does it use Reverse Transcriptase
34
Virus maturation happens after it leaves OR is leaving the host cell, it's the...
cleavage of protein
35
How are the virus genomes selected from all of the nucleic acid that might be present in an infected cell?
from specific protein---nucleic acid interactions (e.g: spliceosomes remove introns)
36
Virus capsid doesn't package host cell's nucleic acid, but in SOME cases it may package...
tRNA that is used as a primer for RT (HIV)
37
How would a mis-sense or non-sense mutation in a gene encoding a capsid protein result in the failure of a virus particles being produced during an infection?
mean that the virus could not assemble the components it needed for virus protein (i.e., no capsid protein or capsid proteins that don’t fit together. If the capsid cannot be assembled, the virus won’t be able to egress from the celll)
38
What usually ends a productive infection cycle?
the release of infectious virus particle
39
A new virus is able to infect a monkey cell but not a human cell when cultured in the laboratory. However, if the genome is extracted and then micro-injected into a human cell, a productive infection will occur. In other words, progeny viruses are produced. Is the human cell susceptible and/or permissive?
its permissive but not susceptible
40
For a DNA virus that replicates in the cytoplasm of the host cell, what is the on enzyme it must have packaged in its capsid to ensure its replication in the host cell? What enzyme is also likely to be present
Bring it's own RNA Pol Sometimes DNA pol to speed up the process