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Basal
bodystructureC.
Characteristics
of
MTaasssseemmbbllyyDynamicinstability
duethe
structuraldifferencesbetween
a
growinand
a
shrinkingmicrotubule
end.GTP
cap;Catastrophe:accidental
lossGTP
cap;Rescue:
regainof
GTP
cap·
Why
the
centrosome
can
act
as
MTOCStructureNo
centriolesin
Plant
andfungi·
Experiments
supporting
thatcentrosome
is
the
MTOCTreat
cell
withcolcemidCytosolic
MTs
depoly,
except
those
in
centrosomeRemovecolcemidTublin
repolyExpla
I:
MTOC
nucleatepoly
of
tubulinsExpla
II:
MTOC
gatherMTs
in
cytosolB
centrosome+TubulinsMT+TubulinsNoA·MT
are
nucleated
by
a
protein
complexcontaining
-tubulinThe
centrosome
is
the
major
MTOC
of
animal
cells·
Drugs
affect
the
assembly
of
MTsColchicineBinding
to
tubulin
dimers,
prevent
MTspolymerizationTaxolBinding
to
MTs,
stabilize
MTsThese
compounds
are
called
antimitotic
drugs,
and
haapplication
in
medical
practice
as
anticancer
drugs·
Microtuble-associated
proteins(MAPs)MAPs
modulate
MT
structure,
assembly,and
functionKatanin
like
proteinsMAPsTau:
In
axon,
cause
MTs
to
form
tight
bundlesMAP2:
In
dendrites,
cause
MTs
to
form
looser
bundlesMAP1B:
In
both
axons
and
dendrites
to
form
crossbridgebetween
microtubulesControlorganizatioMAPsMAP1A,
MAP1B,
MAP1CMAP2,
MAP2cMAP3,MAP4TauThe
importance
of
MAPs
for
neurite
formationOrganization
of
MT
bundles
by
MAPs
.Spacingof
MTs
depends
on
MAPsInsect
cell
expressiIngsect
cell
expressingMAP2
tauFrom
J.
Chen
et
al.
1992.
Nature
360:
674The
effects
of
proteins
that
bind
to
MT
ends(A)The
transitibetween
Mtgrowth
and
Mtshrinking
iscontrolled
in
cby
specialproteins.(B)Cappingproteins
help
tlocalize
Mt
inbudding
yeastcell.5.
Functions
ofMTs1.
Maintain
cell
shapeFig.
10-31
Microtubule
dynamics
in
a
living
cell.
A
fibroblast
was
injwith
tubulin
that
had
been
covalently
linked
to
rhodamine,
so
that
approxim1
tubulin
subunit
in
10
in
the
cell
was
labeled
with
a
fluorescent
dye.
Noteexample,
that
microtubule
#1
first
grows
and
then
shrinks
rapidly,
whereasmicrotubule
#4
grows
continuously.
(P.J.
Sammak
et
al.,
Nature
332:
724-73细胞内物质运输Motor
ProteinKinesin
FamilyDynein
Family染色体运动Intermediate
filaments,IFsIFs
are
the
most
abundant
andstable
components
of
thecytoskeletonFigure
10-13
The
domain
organization
of
intermediate
filamprotein
monomers. Most
intermediate
filament
proteins
shasimilar
rod
domain
that
is
usually
about
310
amino
acids
longforms
an
extended
alpha
helix.
The
amino-terminal
and
carboxyterminal
domains
are
non-alpha-helical
and
vary
greatly
in
siand
sequence
in
different
intermediate
filaments.Figure
10-14.
A
current
model
of
intermediate
filamentconstruction.Figure
10
–16.
Electron
micrographs
of
two
types
of
intermediatefilaments
in
cells
of
the
nervous
system.
(A)
Freeze-etch
image
ofneurofilaments
in
a
nerve
cell
axon,
showing
the
extensive
cross-linkingthrough
protein
cross-bridges
.
(B)
Freeze-etch
image
of
glial
filaments
icells
illustrating
that
these
filaments
are
smooth
and
have
few
cross-bridConventional
electron
micrograph
of
a
cross-section
of
an
axon
showing
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