Chemistry Reference
In-Depth Information
Silaffin-1A
1
NH
2
SSK
K
S
G
S
Y
S
G
S
K
G
S
K
COOH
OH
NH
N
N
NH
NH
NH
n = 4-9
n=4-9
N
N
N
N
Silaffin-1A
2
NH
2
SSK
K
S
G
S
Y
S
G
Y
S
T
K
K
S
GSK
COOH
HO
N
NH
NH
N
NH
NH
n = 4-9
n=4-9
N
N
N
N
Fig. 3.1
The chemical structures of silaffin-1A
1
and silaffin-1A
2
. The post-translationally modi-
fied lysine residues contribute to the structure directing activity of the silaffins [
2
,
9
]
The silica precipitating action of silaffin-1A is dependent on these post-trans-
lationally modified lysine residues [
2
]. Silica precipitation assays using silaffin
preparations with a metastable silicic acid solution produced silica within seconds
[
1
]. The silaffins co-precipitated with silica suggesting that they act in a structure
directing role.
The silacidins on the other hand are rich in aspartate/glutamate and phosphorylated
serine residues that make them anionic at neutral pH [
3
]. These peptides produced
silica, when combined with polyamines, in a concentration dependent manner and it
has been hypothesized that these proteins are the biological anion required to direct
that precipitation of silica
in vivo
.