Accuracy of protein secondary structure determination from circular dichroism spectra based on immunoglobulin examples

• Published in: Analytical biochemistry 2003-10, Vol.321 (2), p.183-187
• Main Authors: Tetin, Sergey Y, Prendergast, Franklyn G, Venyaminov, Sergei Yu
• Format: Article
• Language: English
• Subjects: Circular Dichroism - methods; Comparison of circular dichroism and X-ray analysis; Immunoglobulin Fab Fragments - chemistry; Monoclonal antibody; Protein Structure, Secondary; Proteins - chemistry; Secondary structure; Sensitivity and Specificity
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1016/S0003-2697(03)00458-5

Strong contribution of the aromatic amino acid side chain chromophores to the far-UV circular dichroism (CD) spectra substantially distorts a relatively weak CD signal originating from β sheet, the main type of immunoglobulin secondary structure. In this study we compared the secondary structure calculated from the far-UV CD spectra with the X-ray data for three antibody Fab fragments. Calculations were performed with three different algorithms, using two sets of reference proteins. Low standard deviations between all six estimates indicate stable mathematical solutions. Despite pronounced differences in the shape and amplitude of the CD spectra, we found a strong correlation between CD and X-ray data in the secondary structure for every protein studied. The number and average length of the secondary structure elements estimated from the CD spectra closely resemble those of the X-ray data. Agreement between spectroscopic and crystallographic results demonstrates that modern methods of secondary structure calculation are resilient to distortions of the far-UV CD spectra of immunoglobulins caused by aromatic side chain chromophores.