| Literature DB >> 33058881 |
Jelena Cveticanin1, Tridib Mondal2, Elizabeth M Meiering3, Michal Sharon4, Amnon Horovitz5.
Abstract
About 20% of all familial amyotrophic lateral sclerosis (ALS) cases are associated with mutations in superoxide dismutase (SOD1), a homodimeric protein. The disease has an autosomal-dominant inheritance pattern. It is, therefore, important to determine whether wild-type and mutant SOD1 subunits self-associate randomly or preferentially. A measure for the extent of bias in subunit association is the coupling constant determined in a double-mutant cycle type analysis. Here, cell lysates containing co-expressed wild-type and mutant SOD1 subunits were analyzed by native mass spectrometry to determine these coupling constants. Strikingly, we find a linear positive correlation between the coupling constant and the reported average duration of the disease. Our results indicate that inter-subunit communication and a preference for heterodimerization greatly increase the disease severity.Entities:
Keywords: amyotrophic lateral sclerosis; double-mutant cycles; native mass spectrometry; protein interactions; superoxide dismutase
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Year: 2020 PMID: 33058881 DOI: 10.1016/j.jmb.2020.09.025
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469