pH Sensitivity of the SERF1a Conformational Ensemble
The MOAG-4/SERF class of proteins is a positive regulator of the aggregate formation of amyloid proteins that play an important role in the origin of numerous age-related diseases. In this class of proteins, previous structural studies showed that SERF1a is a very flexible protein, containing at least one α-helical region. The present work proposes the first description of the conformational space of SERF1a at two pH values (6 and 6.8) using nuclear magnetic resonance (NMR) and small-angle X-ray scattering (SAXS). SERF1a NMR conformations have been generated using the CYANA-FLYA procedure as well as the TAiBP (Threading-Augmented interval Branch-and-Prune) procedure, based on the systematic enumeration of protein conformations within an original distance geometry scheme. The generated conformations were filtered using Pepsi-SAXS by fitting small-angle X-ray experiments based on size exclusion chromatography (SEC-SAXS). At pH 6.8, a good fit of the SEC-SAXS curves was obtained for the CYANA and TAiBP NMR conformations, while at pH 6, analysis of the NMR conformations and the SEC-SAXS curves indicated that there could be a conformational exchange between a compact conformation displaying long-range nuclear Overhauser effects (NOEs) between residues LYS-13 and THR-32, and slightly more extended conformations. The shortening of the C-terminal α-helix, as well as the destabilization of the N-terminal α-helix at acidic pH, may be related to the physiological function of SERF1a in the nucleoli. Interestingly, the N-terminal region of SERF1a displays numerous possible binding pockets, particularly in the region interacting with α-synuclein, detected by chemical shift perturbations. In general, the TAiBP procedure allows for a more expanded exploration of the SERF1a conformational space as well as for a description of the internal dynamics of SERF1a in agreement with NMR relaxation and with predictions from the protein primary sequence.
Authors
- U‐Ser Jeng (ORCID: https://orcid.org/0000-0002-2247-5061)
- Thérèse E. Malliavin (ORCID: https://orcid.org/0000-0002-3276-3366)
- Chang Chi-Fon
- Jung‐Hsin Lin (ORCID: https://orcid.org/0000-0002-6712-4994)
- Shu-Yu Huang
- Orion Shih
Institutions
- National Taiwan University (TW)
- Chang Gung University (TW)
- American Association of Colleges of Pharmacy (US)
- National Tsing Hua University (TW)
- Genomics Research Center, Academia Sinica (TW)
- National Synchrotron Radiation Research Center (TW)
- Research Center for Applied Science, Academia Sinica (TW)
- Laboratoire de Physique et Chimie Théoriques
- Academia Sinica (TW)
- Université de Lorraine (FR)
Publication Details
- Journal
- ACS Omega
- Published
- 2026-01-05
- DOI
- https://doi.org/10.1021/acsomega.5c07620
- Primary Topic
- Alzheimer's disease research and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00