Lecture 3 - Viral Architecture Flashcards

1
Q

What is the virual struture consist of?

A
Nucleic acid (DNA or RNA)
 Outer shell (capsid)
 Nucleocapsid: nucleic acid genome packaged within the capsid
 \+/- Envelope
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2
Q

What is the function of the Viral Capsid?

A
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3
Q

Describe the Capsid Design

A
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4
Q

What are viral capsids?

Capsomers?

A
  • Proteins associate into identical structural units called capsomers or capsomeres.
  • Capsomers are arranged symmetrically around viral genome.
  • Can consist of one type of protein or several different protein subunits.
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5
Q

What is involved in the self- assembly of a virus?

A

Economy and efficiency
Construction and rapid assembly of “basic units”
Sub-assembled structures form and break apart on route to the most stable structure

12 solid yellow pieces represent viral subunits
Magnets represent attractive forces between subunits.
Strength of shaking represents temperature of microenvironment

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6
Q

Describe Virus-like particles

A

Self-assembly sometimes results in particles empty of genetic material
Not infectious, but immunogenic
Vaccine approach; safer alternative to attenuated viruses
Delivery system for genes or other therapeutics

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7
Q

Describe Helical Capsids

A
  • Simplest way to arrange multiple, identical protein subunits is to use rotational symmetry
  • Arrange the irregularly shaped proteins around the circumference of a circle to form a disc
  • Central cavity
  • Length of capsid related to length of nucleic acid within.
  • ssRNA, ssDNA in some cases
  • Diameter dependent on the size and arrangement of capsomers
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8
Q

Describe Icosahedral shape

A

Most animal viruses are icosahedral or near-spherical with icosahedral symmetry
Regular polyhedron with:
20 identical equilateral triangular faces
30 edges
2 vertices
optimal way of forming a closed shell from identical protein sub-units (capsomeres)
minimum of 3 subunits per face(60 total)
Most virions, due to their size, have more than 60 subunits

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9
Q

What is a 5-3-2 axis symmetry?

A

12 five-fold rotation axes
20 three-fold rotational axes
30 two-fold rotational axes

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10
Q

Why do larger viruses assemble in complex packages?

A

True icosaherdron consists of only 20 facets/subunits
Difficult for >60 subunits to be arranged in an equivalent fashion
Casper and Klug (1962)
Quasi-equivalent bonding
Triangulation number: # of subunits per facet or simply 60 x N

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11
Q

What is the triangulation number (T-number)?

A

Number used to describe the relation between the # of:
Pentamers= capsomers at the apices surrounded by 5 other capsomers
Hexamers= capsomers on the triangular faces surrounded by 6 other capsomers
12 subunits x 20 = 240

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12
Q

What is Quasi-equivalent Bonding?

A
  • Attainment of maximum stability is overriding factor determining final structure of a virus particle
  • More economical to use 180 identical subunits to build a capsid than 60 copies each of three different proteins
  • Subunits will not all be in identical positions
  • Distinct binding interactions with nearest neighbors
  • Requirement for nearly-equivalent bonding arrangements
  • “any small variation in regular internal bonding pattern leading to a more stable structure”
Each comma is a subunit
 180 subunits (T=3)
 Head-to-head, neck-to-neck, tail-to-tail interactions
 60 tail-to-tail interactions in clusters of 5 (“A”)
 120 tail-to-tail interactions in clusters of 6 (“B” and “C”)
 Subunits do not need to bind all three places with each other
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13
Q

Why Subunit Construction? What is involved?

A
  1. Necessity: small genome; viruses are 50-90% protein
  2. Self-assembly: free energy minimum
  3. Fidelity: smaller protein means less chance of error occurring
  4. Economy: correct structure can be formed with minimal waste; only small incorrect subunits need to be discarded
  5. Complexity: larger the number of the subunits, the more stable the virus becomes; larger particle means a bigger genome
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14
Q

What kind of influence does the nucleic acid have on the structure?

A
  • ssRNA viruses often possess helical capsid structure
  • Cylinder container allows for direct contact between (-) charged nucleic acid and (+) charged protein subunits
  • Almost all dsDNA viruses have icosahedral symmetry
  • Circular DNA, highly coiled
  • Compact globular structure easily contained within a spherical capsid
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15
Q

The structure of a virus whether it is naked or enveloped

A
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16
Q

Describe Viral Envelopes

A
  • Acquired by budding through a host cell membrane
  • External (plasma membrane)
  • Internal (Golgi)
  • Enveloped virus do not necessarily have to kill their host cell in order to be released
  • Some budding viruses are also persistent
  • Viral envelope proteins synthesized by host ribosomes
  • Inserted into host cell membrane by normal trafficking routes
  • Enveloped viruses are only infectious if the envelope is intact
  • Viral attachment proteins contained in envelope
  • Damage to the envelope may reduce infectivity (alcohols, detergents)
17
Q

What are Viral Spikes?

A
  • Glycoproteins that project from some enveloped viruses are called spikes
  • Viral spikes determine what types of hosts (host range) and cells (tropism) the virus can infect
18
Q

What are complex viruses?

A
  • Unusual morphology
  • Don’t fit the typical helical or icosahedral design
  • Extra structures like tails or outer walls
  • Larger genomes
19
Q

What are Pox Viruses?

A
  • Oval or ‘brick-shaped’ particles 200-400nm long
  • Genome is associated with proteins within a central disk structure known as a nucleoid
  • Nucleoid is surrounded by a membrane
20
Q

What are tailed phages?

A
  • Head consists essentially of an icosahedral shell attached via a collar to a contractile, helical tail (“prolate”).
  • End of the tail is a plate at end of tail functions in attachment to, and penetration of, bacteria.
  • Thin protein fibers attached to the plate involved in binding to receptor molecules on host cell wall.
21
Q

What is the dissembly of viruses?

A

Virions are primed to enter cells and release their genomes
The release of the viral genome can occur by multiple mechanisms:
Proteolytic cleavage of capsid proteins
Unspooling of genome into cell
Interaction of genome with cytoplasmic components