1. Volume 82, Issue 6, Pages 3254-3268 (June 2002)
Oxidized Derivatives of Octopus vulgaris and Carcinus aestuarii Hemocyanins at pH 7.5 and Related Models by X-ray Absorption Spectroscopy 
Elena Borghi, Pier Lorenzo Solari, Mariano Beltramini, Luigi Bubacco, Paolo Di Muro, Benedetto Salvato 
Biophysical Journal 
Volume 82, Issue 6, Pages (June 2002)
DOI: /S (02)
Copyright © 2002 The Biophysical Society Terms and Conditions

2. Figure 1
Comparison of the (A) cubic k-weighted EXAFS and of the (B) corresponding Fourier transforms for the met-Hc and met-azido-Hc derivatives from O. vulgaris and C. aestuarii.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

3. Figure 2
Comparison of the (A) cubic k-weighted EXAFS and of the (B) corresponding Fourier transforms for the [Cu2(L-5,5)(X2)](ClO4)n complexes with X=OH−, H2O, N3−.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

4. Figure 3
Comparison of the (A) cubic k-weighted EXAFS and of the (B) corresponding Fourier transforms for the [Cu2(L-6,6)(X2)](ClO4)n complexes with X=OH−, H2O, N3−.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

5. Figure 4
Comparison of the (A) cubic k-weighted EXAFS and of the (B) corresponding Fourier transforms for the [Cu(2-BB)(H2O)2](PF6)2 and [Cu(2-BB)(N3)]ClO4 complexes.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

6. Figure 5
Results of the best fits of the cubic k-weighted EXAFS for (A) met-Hc and (B) met-azido-Hc derivatives from O. vulgaris and for (C) met-Hc and (D) met-azido-Hc derivatives from C. aestuarii. The total simulated signals (continuous line) are superimposed on the experimental signals (dotted line). At the bottom of panels the residual functions are plotted. The values of Rexp and Rth are reported.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

7. Figure 6
Comparison of the Cu K-edge XANES spectra (upper panel) and of the corresponding XANES derivative spectra (lower panel) for the met-Hc and met-azido-Hc derivatives from O. vulgaris and C. aestuarii. In the derivative spectrum the features (P, α, β, γ, δ, ϵ, φ) are shown.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

8. Figure 7
Comparison of the Cu K-edge XANES spectra (upper panel) and of the corresponding XANES derivative spectra (lower panel) for the [Cu2(L-5,5)(X2)](ClO4)n complexes with X=OH−, H2O, N3−. In the derivative spectrum the features (P, α, β, γ, δ, ϵ, φ) are shown.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

9. Figure 8
Comparison of the Cu K-edge XANES spectra (upper panel) and of the corresponding XANES derivative spectra (lower panel) for the [Cu2(L-6,6)(X2)](ClO4)n complexes with X=OH−, H2O, N3−. In the derivative spectrum the features (P, α, β, γ, δ, ϵ, φ) are shown.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

10. Figure 9
Comparison of the Cu K-edge XANES spectra (upper panel) and of the corresponding XANES derivative spectra (lower panel) for the [Cu(2-BB)(H2O)2](PF6)2 and [Cu(2-BB)(N3)]ClO4 complexes. In the derivative spectrum the features (P, α, β, γ, δ, ϵ, φ) are shown.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions