Biomedical Engineering Reference
In-Depth Information
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Figure 16.7
Binding (raw data) of 500 pM cy3-labelled targets to different areas on a 20-mer capture
probe spotted on glass ( Schultz et al., 2008 ): (a) Area 1, (b) Area 2, (c) Area 3. When only a solid
line (--) is used then a single-fractal analysis applies. When both a dashed (- - -) and a solid (--)
line are used then the dashed line represents a single-fractal analysis and the solid line represents a
dual-fractal analysis.
dimension, D f , for a single-fractal analysis, and (b) the binding rate coefficients, k 1 and k 2 ,
and the fractal dimensions, D f1 and D f2 , for a dual-fractal analysis are given in Table 16.5 .
For a dual-fractal analysis, it is of interest to note that as the fractal dimension increases by a
factor of 1.93 from a value of D f1 equal to 1.2272 to D f2 equal to 2.3698, the binding rate
coefficient increases by a factor of 33.29 from a value of k 1 equal to 0.1629 to k 2 equal to
5.4224. The changes in the degree of heterogeneity or the fractal dimension on the sensor sur-
face and in the binding rate coefficient are in the same direction.
Figure 16.7b shows the binding of 500 pM cy3-labelled target (raw data) to a 20-mer capture
probe immobilized on Area 2 (control) on the microarray biosensor ( Schultz et al., 2008 ).
It shows, once again, that a dual-fractal analysis is required to adequately describe the bind-
ing kinetics. The values of (a) the binding rate coefficient, k , and the fractal dimension, D f ,
for a single-fractal analysis, and (b) the binding rate coefficients, k 1 and k 2 , and the fractal
dimensions, D f1 and D f2 , for a dual-fractal analysis are given in Table 16.5 .
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