{"title":"SOD1的H46R和H80R疾病突变体的稳定性、灵活性和相分离特性研究:ALS发病机制的新见解","authors":"Ahana Banerjee, Dwipanjan Sanyal, Krishnananda Chattopadhyay","doi":"10.1021/acs.biochem.5c00289","DOIUrl":null,"url":null,"abstract":"<p><p>Human Cu, Zn superoxide dismutase (SOD1) is the primary enzyme in the cellular antioxidant defense system. Mutations in SOD1 are associated with amyotrophic lateral sclerosis (ALS), where protein misfolding and aggregation contribute to the disease pathology. Recently, SOD1 mutants have been shown to undergo phase separation, forming protein-rich droplets that can serve as precursors to the fibrillar aggregates, the pathological hallmarks of ALS. Protein phase separation is a critical process for membraneless organelle formation and the regulation of cellular activities, and its disruption is associated with neurodegeneration. In this study, we investigated two ALS-associated SOD1 mutants, H46R and H80R, and compared them to the wild-type (WT) and Apo forms to elucidate the relationship between phase separation and SOD1's biophysical properties. Using computational studies, chemical denaturation, in vitro condensate formation assays, and analyzing their dynamic behavior, we explored how these mutants influence protein phase separation propensity. Our findings demonstrate that altered secondary structures, stability, and inherent disorder in these mutants directly impact their phase separation behaviors. This study provides new insights into the role of phase separation in ALS pathogenesis and its potential as a therapeutic target.</p>","PeriodicalId":28,"journal":{"name":"Biochemistry Biochemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigating the Stability, Flexibility, and Phase Separation Properties of H46R and H80R Disease Mutants of SOD1: Insights into ALS Pathogenesis.\",\"authors\":\"Ahana Banerjee, Dwipanjan Sanyal, Krishnananda Chattopadhyay\",\"doi\":\"10.1021/acs.biochem.5c00289\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Human Cu, Zn superoxide dismutase (SOD1) is the primary enzyme in the cellular antioxidant defense system. Mutations in SOD1 are associated with amyotrophic lateral sclerosis (ALS), where protein misfolding and aggregation contribute to the disease pathology. Recently, SOD1 mutants have been shown to undergo phase separation, forming protein-rich droplets that can serve as precursors to the fibrillar aggregates, the pathological hallmarks of ALS. Protein phase separation is a critical process for membraneless organelle formation and the regulation of cellular activities, and its disruption is associated with neurodegeneration. In this study, we investigated two ALS-associated SOD1 mutants, H46R and H80R, and compared them to the wild-type (WT) and Apo forms to elucidate the relationship between phase separation and SOD1's biophysical properties. Using computational studies, chemical denaturation, in vitro condensate formation assays, and analyzing their dynamic behavior, we explored how these mutants influence protein phase separation propensity. Our findings demonstrate that altered secondary structures, stability, and inherent disorder in these mutants directly impact their phase separation behaviors. This study provides new insights into the role of phase separation in ALS pathogenesis and its potential as a therapeutic target.</p>\",\"PeriodicalId\":28,\"journal\":{\"name\":\"Biochemistry Biochemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemistry Biochemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.biochem.5c00289\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry Biochemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.biochem.5c00289","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Investigating the Stability, Flexibility, and Phase Separation Properties of H46R and H80R Disease Mutants of SOD1: Insights into ALS Pathogenesis.
Human Cu, Zn superoxide dismutase (SOD1) is the primary enzyme in the cellular antioxidant defense system. Mutations in SOD1 are associated with amyotrophic lateral sclerosis (ALS), where protein misfolding and aggregation contribute to the disease pathology. Recently, SOD1 mutants have been shown to undergo phase separation, forming protein-rich droplets that can serve as precursors to the fibrillar aggregates, the pathological hallmarks of ALS. Protein phase separation is a critical process for membraneless organelle formation and the regulation of cellular activities, and its disruption is associated with neurodegeneration. In this study, we investigated two ALS-associated SOD1 mutants, H46R and H80R, and compared them to the wild-type (WT) and Apo forms to elucidate the relationship between phase separation and SOD1's biophysical properties. Using computational studies, chemical denaturation, in vitro condensate formation assays, and analyzing their dynamic behavior, we explored how these mutants influence protein phase separation propensity. Our findings demonstrate that altered secondary structures, stability, and inherent disorder in these mutants directly impact their phase separation behaviors. This study provides new insights into the role of phase separation in ALS pathogenesis and its potential as a therapeutic target.
期刊介绍:
Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.