Biology Reference
In-Depth Information
Most virus capsids consist of identical copies of coat
proteins. However, there are also capsids that are formed by several different
coat proteins. In
The P numbers.
(CPMV) two different coat proteins form
the capsid, the small (S) and large (L) coat protein subunits. The S protein
is a one-domain (A domain) and the L protein is a two-domain protein (B
and C domains). The three domains can be arranged in so-called
Cowpea mosaic virus
pseudo
-
equivalence. The
T
numbers are assigned as
pseudo T
or
P
numbers. CPMV
has
= 3 symmetry and consists of 60 copies of each coat protein subunit
(Fig. 2.6; Lin, T., Chen, Z., Usha, R., Stauffacher, C. V., Dai, J. B., Schmidt, T., and
Johnson, J. E. (1999) The refined crystal structure of cowpea mosaic virus at
2.8 Å resolution,
P
(1), 20-34.).
Tuning capsid symmetry using nanotechnology.
Virology
,
265
Nanotechnology
has been applied as a technique to understand virus assembly. In particular,
synthetic nanoparticles can be used as cores to nucleate assembly of BMV
particles (Chen
et al
., 2006; Dixit
et al
., 2006; Dragnea
et al
., 2003; Sun
et
al
., 2007) (see Chapter 5). Assessing whether the morphology of the capsid
could be tuned using different-sized nanoparticle cores, it was found that
the capsid symmetry indeed is dependent on the nanoparticle core size.
Incorporated gold cores of 9 nm yielded particles similar to
pseudo
T
= 2
symmetry,
= 1 symmetry, and
particles with cores of a size of 12 nm resulted in particles similar to native
particles with
1
particles with gold cores of 6 nm size showed
T
., 2007). Studies along these lines are
expected to provide further insights into the fundamental understanding of
viral self-assembly.
T
= 3 symmetry (Sun
et al
2.1.2.2 Rod-shaped VNPs: helical tubes and ilamentous structures
Icosahedral particles are relatively more common than rod-shaped or
filamentous structures. There are, however, a number of rod-shaped particles
relevant to nanotechnology including:
Tobacco mosaic virus
(TMV),
Potato
virus X
(PVX), M13, and
Sulfolobus islandicus
rod-shaped virus 2 (SIRV2) (for
example, see references: Carette
et al
., 2007; Lee
et al
., 2009; Mao
et al
., 2004;
Nam
et al
., 2006, 2008; Schlick
et al
., 2005; Shenton
et al
., 1999; Steinmetz
et
al
., 2008; Tseng
et al
., 2006; Yi
et al
., 2007; Yoo
et al
., 2006).
1
T
= 2 symmetry is typically referred to as
pseudo T
= 2 symmetry. According to the model by
Kasper and Klug (see Eq. 1), a
= 2 would not be feasible. However, proteins and potein-protein
interactions are flexible — also allowing symmetries that would not have been predicted using
mathematical models.
T
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