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The functional diversity of proteins often arises from the remodeling of conformational ensembles, particularly through mutations and post-translational modifications (PTMs). However, experimentally characterizing such ensembles remains challenging due to their heterogeneous and transient nature. Here, we report the determination of the conformational substates of β-sheets and the effect associated with mutations and PTMs in human islet amyloid polypeptide (hIAPP) via scanning tunneling microscopy (STM). Thanks to the ultrahigh resolution of STM, the β-sheets formed by the assembly of hIAPP were revealed to be conformationally diverse, including 17 types of conformational substates concomitant with 60 types of interconformation interactions. These conformational substates are highly heterogeneous in the folding structures but close in energy. Four mutations and PTMs were carried out with hIAPP to investigate the evolvability of the β-sheet assembly. Regulation effects accomplished by the mutations and PTMs on the conformational ensembles of β-sheets have been identified, including the number of conformational substates, the most probable substates, and the topography of the energetic landscapes of inter-β-strand interactions. Different types of variations show divergence in the influences on the β-sheet conformational ensembles, which is correlated with the divergent aggregation propensity. Our results highlight the plasticity of conformational ensembles upon mutations and PTMs.
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http://dx.doi.org/10.1021/acscentsci.5c00421 | DOI Listing |
Biochem J
September 2025
Department of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur Campus, Mohanpur, 741246 Nadia, West Bengal, India.
Transcription initiation factor TFIID subunit 1 (TAF1) is a pivotal component of the TFIID complex, critical for RNA polymerase II-mediated transcription initiation. However, the molecular basis by which TAF1 recognizes and associates with chromatin remains incompletely understood. Here, we report that the tandem bromodomain module of TAF1 engages nucleosomal DNA through a distinct positively charged surface patch on the first bromodomain (BD1).
View Article and Find Full Text PDFMol Ther Nucleic Acids
September 2025
Department of Synthetic Biology and Immunology, National Institute of Chemistry, Hajdrihova 19, 1000 Ljubljana, Slovenia.
Loss-of-function mutations in the gene cause β-catenin deficiency, resulting in CTNNB1 syndrome, a rare neurodevelopmental disorder characterized by motor and cognitive impairments. Given the wide variety of mutations across and its dosage sensitivity, a mutation-independent therapeutic approach that preserves endogenous gene regulation is critically needed. This study introduces spliceosome-mediated RNA -splicing as a novel approach to restore β-catenin production.
View Article and Find Full Text PDFBiochim Biophys Acta Mol Basis Dis
August 2025
CHDI Management, Inc., the company that manages the scientific activities of CHDI Foundation, Inc., Los Angeles, USA. Electronic address:
Huntington's disease is a neurodegenerative disorder associated with a polyglutamine expansion within the first exon of the huntingtin protein (HTT exon 1). This mutation results in HTT dysfunction and the production of N-terminal HTT aggregates. The dimerization of the HTT exon 1 fragment through self-association of the first 17 residues (N17) is considered the initial step in the HTT exon 1 aggregation pathway.
View Article and Find Full Text PDFBiochem Soc Trans
August 2025
Department of Biochemistry, The University of Western Ontario, London, ON, N6A 5C1, Canada.
Parkin, a Ring-InBetweenRING-Rcat E3 ubiquitin ligase, plays a vital role in the clearance of damaged mitochondria (mitophagy) by ubiquitylating a broad spectrum of mitochondrial proteins. Mutations in the PRKN gene alter parkin ubiquitylation activity and are a leading cause of early-onset Parkinsonism, underlining its critical function in maintaining mitochondrial homeostasis. The structures, substrates, and ubiquitylation mechanisms used by parkin in mitophagy are well established.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Biological Sciences, Beck College of Sciences and Mathematics, Arkansas State University, Jonesboro, Arkansas, USA.
Post-translational modifications (PTMs), such as protein phosphorylation, are critical regulators of bacterial physiology. Here, we present the first comprehensive phosphoproteomic analysis of , revealing extensive -phosphorylation under non-stressed conditions. Using tandem mass tag (TMT)-based mass spectrometry and phosphopeptide enrichment, we identified 231 high-confidence phosphosites on 131 proteins, representing approximately 6.
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