Books:
Mechanisms of Protein Folding, 2nd edn., (2000) R. H. Pain (ed.), Oxford University Press.
Protein Folding-Misfolding: some current concepts of protein chemistry. Zbilut JP and Scheibel T (eds.), Nova Sci Publi., New York, 2007.
Protein misfolding diseases; current and emerging therapies. eds Raminez-Alvarado, J.W. Kelly, C.M. Dobson, Wiley Series in Protein and Peptide Science, Series Ed. V.N. Uversky. John Wiley & Sons, New Jersey 2010.
Selected papers:
Lion et al., 2021. A framework for understanding the functions of biomolecular condensates across scales. Nat Rev Mol Cell Biol, 2021 Mar;22(3):215-235. doi: 10.1038/s41580-020-00303-z.
ŽEROVNIK, Eva. Viroporins vs. other pore-forming proteins : what lessons can we take. Frontiers in chemistry, ISSN 2296-2646. [Online ed.], 2021, vol. 9, str. 626059-1-626059-6, doi: 10.3389/fchem.2021.626059.
issue: http://www.mdpi.com/journal/biomolecules/special_issues/protein-folding#published
Eichner T, Kalverda AP,. Thompson GS, Homans SW. and Radford SE (2011) Conformational Conversion during Amyloid Formation at Atomic Resolution. Molecular Cell 41: 161-172.
Sharma, S. et al. (2008). Monitoring protein conformation along the pathway of chaperone-assisted folding. Cell, 133,142-153.
Felitsky et al., (2008). Modeling transient collapsed states of an unfolded protein to provide insights into early folding events. Proc. Natl. Acad. Sci USA 105: 6278-6283.
Žerovnik E, Stoka V, Mirtič A, Gunčar G, Grdadolnik J, Staniforth RA, Turk D, Turk V. (2011). Mechanisms of amyloid fibril formation--focus on domain-swapping. FEBS J. 278:2263-82. doi: 10.1111/j.1742- 4658.2011.08149.x. Epub 2011 May 31. Review.
Di Scala e tal., (2016) Common molecular mechanism of amyloid pore formation by Alzheimer's b- amyloid peptide and a-synuclein Scien. Reports, DOI: 10.1038/srep28781.
Sengupta U, Nilson N.A., Kayed R., The role of amyloid-b oligomers in toxicity, propagation, and immunotherapy EBioMedicine , 2016, vol6, 42-49."""