Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10537362 | Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics | 2005 | 8 Pages |
Abstract
Using far and near-UV CD, ANS fluorescence and 2D NMR spectroscopy, an acid-induced partly folded state (A state) at extremely low pH for hUBF HMG Box1 was identified and characterized. As compared to the native state (N), the A state has similar secondary structure, less compact pack with larger amounts of exposed hydrophobic surface, and narrower chemical shift dispersion in 1H-15N HSQC spectrum, which implies that it is a molten globule (MG)-like species. On the other hand, substantial tertiary contacts and cooperative thermal denaturing transition indicate that the A state is closer-relative to the classic MG-to the native folded state. In addition, when the solution pH is adjusted to neutrality, the protein in the A state refolds to the native state easily. All these data suggest that the A state of hUBF HMG Box1 could represent a potential folding intermediate on protein folding pathway.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Xuecheng Zhang, Jiahai Zhang, Xuan Li, Junjie Xu, Hongda Huang, Quan Chen, Jihui Wu, Yunyu Shi,