| Literature DB >> 36271180 |
Marisol Gouveia1, Cristine Schmidt2,3,4, Manuel Teixeira1, Mário Lopes5, Susana S Aveiro6,7, Pedro Domingues6, Ke Xia8,9, Wilfredo Colón8,9, Rui Vitorino1,2, Rita Ferreira10, Mário Santos4,11,12, Sandra Vieira1, Fernando Ribeiro13.
Abstract
This study characterizes the plasma levels and composition of SDS-resistant aggregates (SRAs) in patients with heart failure with preserved ejection fraction (HFpEF) to infer molecular pathways associated with disease and/or proteostasis disruption. Twenty adults (ten with HFpEF and ten age-matched individuals) were included. Circulating SRAs were resolved by diagonal two-dimensional SDS-PAGE, and their protein content was identified by mass spectrometry. Protein carbonylation, ubiquitination and ficolin-3 were evaluated. Patients with HFpEF showed higher SRA/total (36.6 ± 4.9% vs 29.6 ± 2.2%, p = 0.009) and SRA/soluble levels (58.6 ± 12.7% vs 40.6 ± 5.8%, p = 0.008). SRAs were carbonylated and ubiquitinated, suggesting they are composed of dysfunctional proteins resistant to degradation. SRAs were enriched in proteins associated with cardiovascular function/disease and with proteostasis machinery. Total ficolin-3 levels were decreased (0.77 ± 0.22, p = 0.041) in HFpEF, suggesting a reduced proteostasis capacity to clear circulating SRA. Thus, the higher accumulation of SRA in HFpEF may result from a failure or overload of the protein clearance machinery.Entities:
Keywords: Aggregates; Bioinformatics; Cardiovascular disease; Mass spectrometry; Proteostasis
Year: 2022 PMID: 36271180 DOI: 10.1007/s12265-022-10334-w
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 3.216