Biomedical Engineering Reference
In-Depth Information
adhesion can be significantly influenced by glycocalyx [
64
-
66
], we hypothesize
that cell surface repellers such as glycocalyx may also play a role in the phenome-
non of critical bond spacing. To address this issue, we considered an alternative
model of cell adhesion via opposing forces induced by polymer repellers and
ligand-receptor bonds, where we treat repellers and binders as worm-like chains
confined in a nanoslit in which ligand-receptor bonds transition stochastically
between open and closed states.
When a free polymer chain of contour length
L
, persistence length
p
, and mean-
squared radius of gyration
R
g
[
67
] to be confined inside a nanoslit of separation
h
,a
force
f
will be imposed on the opposing parallel walls. This force can be derived
based on the free energy expression given by Chen and Sullivan [
68
], which
appears as a repulsive force when
h<<L
.
In the case that the two ends of the polymer chain are tethered to the opposing
walls of the slit, the effect of end tethering is expected to be small for
h !
0. In the
opposite limit of
h ! L
, the chain becomes strongly stretched, and its force-
separation relationship can be given by the classical Marko and Siggia formula
[
69
]. For the intermediate range 0
< h < L
, we propose an interpolating formula
on the force-separation relation [
39
]:
"
#
k
B
T
p
1
4
ð
1
h=LÞ
1
4
h
2
L
2
R
g
k
B
T
f ðh; p; LÞ¼
2
p
2
2
þ c
1
ðp=hÞþc
2
ðp=hÞ
(8.12)
5
=
3
2
6
h
3
½
1
þ c
3
ðp=hÞþc
4
ðp=hÞ
It can be easily verified that (
8.12
) matches the above-mentioned two limiting
cases of
h !
0 and
h ! L
.
Similar to the model as shown in Fig.
8.1
, we consider the molecular adhesion
mediated by polymer repellers of density
r
g
and binders of density
r
0
, among which
r
b
of them are actually closed. We adopt a rebinding rate per unit area of
g ¼ k
0
g
ðr
0
r
b
Þ
. Thus, (
8.4
) at steady state can be changed into
gðr
0
r
b
Þ¼
e
f ðh
eq
;L;pÞ=F
b
r
b
(8.13)
On the other hand, the stability of adhesion is considered as a competition
between attractive interactions of ligand-receptor binding and repulsive forces
due to the size mismatch between repellers and binders. According to (
8.12
), the
repulsive stress of polymer repellers and the attractive stress of the molecular bonds
can be expressed as
s
g
¼ r
g
f ðh
eq
; p
g
; L
g
Þ
and
s
b
¼ r
b
f ðh
eq
; p
b
; L
b
Þ
, which must
balance, i.e.,
s
b
¼ s
g
(8.14)
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