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Depletion of pH dependence upon removal of amino acids
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
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Manuscript (Other academic)
URN: urn:nbn:se:su:diva-25427OAI: diva2:199691
Part of urn:nbn:se:su:diva-8146Available from: 2008-09-04 Created: 2008-09-04 Last updated: 2010-01-13Bibliographically approved
In thesis
1. The birth and growth of the protein folding nucleus: Studies of protein folding focused on critical contacts, topology and ionic interactions
Open this publication in new window or tab >>The birth and growth of the protein folding nucleus: Studies of protein folding focused on critical contacts, topology and ionic interactions
2008 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Proteins are among the most complex molecules in the cell and they play a major role in life itself. The complexity is not restricted to just structure and function, but also embraces the protein folding reaction. Within the field of protein folding, the focus of this thesis is on the features of the folding transition state in terms of growing contacts, common nucleation motifs and the contribution of charged residues to stability and folding kinetics.

During the resent decade, the importance of a certain residue in structure formation has been deduced from Φ-value analysis. As a complement to Φ-value analysis, I present how scatter in a Hammond plot is related to site-specific information of contact formation, Φ´(βTS), and this new formalism was experimentally tested on the protein L23. The results show that the contacts with highest Φ growth at the barrier top were distributed like a second layer outside the folding nucleus. This contact layer is the critical interactions needed to be formed to overcome the entropic barrier.

Furthermore, the nature of the folding nucleus has been shown to be very similar among proteins with homologous structures and, in the split β-α-β family the proteins favour a two-strand-helix motif. Here I show that the two-strand-helix motif is also present in the ribosomal protein S6 from A. aeolicus even though the nucleation and core composition of this protein differ from other related structure-homologues.

In contrast to nucleation and contact growth, which are events driven by the hydrophobic effect, my most recent work is focused on electrostatic effects. By pH titration and protein engineering the charge content of S6 from T. thermophilus was altered and the results show that the charged groups at the protein surface might not be crucial for protein stability but, indeed, have impact on folding kinetics. Furthermore, by site-specific removal of all acidic groups the entire pH dependence of protein stability was depleted.

Place, publisher, year, edition, pages
Stockholm: Institutionen för biokemi och biofysik, 2008. 73 p.
protein folding, protein stability, two-state folding, chevron plot, transition-state movements, Hammond behaviour, topology, electrostatic interactions, pH dependence, mass-action, protein engineering, pKa
National Category
Biochemistry and Molecular Biology
Research subject
urn:nbn:se:su:diva-8146 (URN)978-91-7155-704-9 (ISBN)
Public defence
2008-09-26, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 12 A, Stockholm, 13:00
Available from: 2008-09-04 Created: 2008-09-04Bibliographically approved

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