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Relini, A.

Publications and source records attributed to Relini, A..

2 recordsLinked to original sources

Extracellular chaperones modulate AL light chains fibrillar aggregation and contribute to amyloid structural heterogeneity

In AL amyloidosis, monoclonal immunoglobulin light chains (LCs) aggregate as amyloid fibrils in tissues. In synergy with the intrinsic aggregation propensity of specific LC sequences, microenvironment factors may be involved in tuning the disease pathophysiology, in particular proteolytic LC remodelling and heterotypic interactions in the extracellular milieu. Accounting for extrinsic modulators is critical for understanding the phenotypic variability of AL, usually imputed mainly to the LC diversity. We investigated the effects of apolipoprotein E (allele 3, apoE3) and clusterin (CLU), two amyloid-signature proteins involved in extracellular proteostasis, on the fibrillogenesis kinetics of amyloidogenic LC fragments from patient-derived sequences, as well as on aggregate composition, fibril morphology and thermodynamic stability. We show that apoE3 and CLU act as heterotypic interactors of prefibrillar and fibrillar LCs, significantly modulating LC amyloidogenesis, with complex and non-monotypic effects that range from anti- to pro-amyloidogenic depending on their concentration and on the LCs intrinsic amyloidogenicity. ApoE3 and CLU also influence fibril morphology, possibly by modifying protofilament association, and alter their thermodynamic properties. LC interactors may play a significant and insofar underappreciated role in the AL pathophysiology in vivo, likely contributing to phenotypic variability and structural polymorphisms and, possibly, to fibril resilience to amyloid reabsorption strategies.

biochemistry↗

Cholesterol-containing liposomes decorated with Au nanoparticles as minimal tunable fusion machinery

Membrane fusion is essential for the basal functionality of eukaryotic cells. In physiological conditions, fusion events are regulated by a wide range of specialized proteins, as well as by a finely tuned local lipid composition and ionic environment. SNARE proteins, for example, provide the mechanical energy necessary to achieve vesicle fusion in neuromediator release, and their action is assisted by other soluble proteins, membrane cholesterol, and calcium ions. Similar cooperative effects must be explored when considering synthetic approaches to achieve controlled and selective membrane fusion. Here we show that liposomes decorated with amphiphilic Au nanoparticles (AuLips) can act as minimal tunable fusion machinery. AuLips fusion is triggered by divalent ions, while the number of fusion events dramatically depends on, and can be finely tuned by, the liposome cholesterol content. Our results, obtained via a combination of experimental (Quartz-Crystal-Microbalance with Dissipation monitoring, Fluorescence assays, Small-Angle X-ray Scattering) and computational techniques (Molecular Dynamics with coarse-grained resolution), reveal new mechanistic details on the fusogenic activity of amphiphilic Au nanoparticles in synergy with membrane cholesterol, and demonstrate the ability of these synthetic nanomaterials to induce fusion regardless of the divalent ion used (Ca2+ or Mg2+). This evidence provides a novel contribution to the development of new artificial fusogenic agents for next-generation biomedical applications that require tight control of the rate of fusion events (e.g., targeted drug delivery).

biophysics↗