| Literature DB >> 27861798 |
Michal Chojnacki1, Daoning Zhang2, Monika Talarowska3, Piotr Gałecki3, Janusz Szemraj1, David Fushman2, Mark A Nakasone2.
Abstract
The ubiquitin mutant UBB+1 has been identified as a hallmark of neurodegenerative diseases. In this study, we characterize polyubiquitinated forms of UBB+1 in vitro and from patient samples. The ability of UBB+1 to be readily ubiquitinated by several E2 enzymes provided a mechanism for the controlled synthesis and purification of defined conjugates. This allowed us to utilize polyUb-UBB+1 conjugates for biochemical assays, as well as solution NMR. Coupled with our immunoassay for detection of ubiquitinated forms of UBB+1 in patient blood samples, we gain a clearer picture of the molecular mechanisms underlying neurodegenerative diseases.Entities:
Keywords: zzm321990UBBzzm321990+1zzm321990; biomolecular NMR; deubiquitinase; neurodegeneration; polyubiquitin
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Year: 2016 PMID: 27861798 PMCID: PMC5182158 DOI: 10.1002/1873-3468.12484
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124