Sonia Vega

Mrs. Sonia Vega


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 April 2021 in Biomedicines
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Bruno RizzutiBruno Rizzuti
Bruno Rizzuti
Fedora GrandeFedora Grande
Fedora Grande
Filomena ConfortiFilomena Conforti
Filomena Conforti
AJAna Jimenez-Alesanco
Ana Jimenez-Alesanco
LCLaura Ceballos
Laura Ceballos
AVAdrian Velazquez-Campoy
Adrian Velazquez-Campoy
The pandemic, due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has stimulated the search for antivirals to tackle COVID-19 infection. Molecules with known pharmacokinetics and already approved for human use have been demonstrated or predicted to be suitable to be used either directly or as a base for a scaffold-based drug design. Among these substances, quercetin is known to be a potent in vitro inhibitor of 3CLpro, the SARS-CoV-2 main protease. However, its low in vivo bioavailability calls for modifications to its molecular structure. In this work, this issue is addressed by using rutin, a natural flavonoid that is the most common glycosylated conjugate of quercetin, as a model. Combining experimental (spectroscopy and calorimetry) and simulation techniques (docking and molecular dynamics simulations), we demonstrate that the sugar adduct does not hamper rutin binding to 3CLpro, and the conjugated compound preserves a high potency (inhibition constant in the low micromolar range, Ki = 11 μM). Although showing a disruption of the pseudo-symmetry in the chemical structure, a larger steric volume and molecular weight, and a higher solubility compared to quercetin, rutin is able to associate in the active site of 3CLpro, interacting with the catalytic dyad (His41/Cys145). The overall results have implications in the drug-design of quercetin analogs, and possibly other antivirals, to target the catalytic site of the SARS-CoV-2 3CLpro.

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FMFrancesca Mangiavacchi
Francesca Mangiavacchi
PBPaweł Botwina
Paweł Botwina
EMElena Menichetti
Elena Menichetti
LBLuana Bagnoli
Luana Bagnoli
OROrnelio Rosati
Ornelio Rosati
Claudio SantiClaudio Santi
Claudio Santi
The development of new antiviral drugs against SARS-CoV-2 is a valuable long-term strategy to protect the global population from the COVID-19 pandemic complementary to the vaccination. Considering this, the viral main protease (Mpro) is among the most promising molecular targets in light of its importance during the viral replication cycle. The natural flavonoid quercetin 1 has been recently reported to be a potent Mpro inhibitor in vitro, and we explored the effect produced by the introduction of organoselenium functionalities in this scaffold. In particular, we report here a new synthetic method to prepare previously inaccessible C-8 seleno-quercetin derivatives. By screening a small library of flavonols and flavone derivatives, we observed that some compounds inhibit the protease activity in vitro. For the first time, we demonstrate that quercetin (1) and 8-(p-tolylselenyl)quercetin (2d) block SARS-CoV-2 replication in infected cells at non-toxic concentrations, with an IC50 of 192 μM and 8 μM, respectively. Based on docking experiments driven by experimental evidence, we propose a non-covalent mechanism for Mpro inhibition in which a hydrogen bond between the selenium atom and Gln189 residue in the catalytic pocket could explain the higher Mpro activity of 2d and, as a result, its better antiviral profile.

1 September 2021 in Pharmaceuticals
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Bruno RizzutiBruno Rizzuti
Bruno Rizzuti
LCLaura Ceballos
Laura Ceballos
DADavid Ortega Alarcon
David Ortega Alarcon
AJAna Jimenez-Alesanco
Ana Jimenez-Alesanco
SVSonia Vega
Sonia Vega
AVAdrian Velazquez-Campoy
Adrian Velazquez-Campoy
Inhibiting the main protease 3CLpro is the most common strategy in the search for antiviral drugs to fight the infection from SARS-CoV-2. We report that the natural compound eugenol is able to hamper in vitro the enzymatic activity of 3CLpro, the SARS-CoV-2 main protease, with an inhibition constant in the sub-micromolar range (Ki = 0.81 μM). Two phenylpropene analogs were also tested: the same effect was observed for estragole with a lower potency (Ki = 4.1 μM), whereas anethole was less active. The binding efficiency index of these compounds is remarkably favorable due also to their small molecular mass (MW < 165 Da). We envision that nanomolar inhibition of 3CLpro is widely accessible within the chemical space of simple natural compounds.

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SVSonia Vega
Sonia Vega
JNJosé L. Neira
José L. Neira
Carlos MarcuelloCarlos Marcuello
Carlos Marcuello
Anabel LostaoAnabel Lostao
Anabel Lostao
Olga AbianOlga Abian
Olga Abian
AVAdrian Velazquez-Campoy
Adrian Velazquez-Campoy
The nonstructural protein 3 (NS3) from the hepatitis C virus (HCV) is responsible for processing the non-structural region of the viral precursor polyprotein in infected hepatic cells. NS3 protease activity, located at the N-terminal domain, is a zinc-dependent serine protease. A zinc ion, required for the hydrolytic activity, has been considered as a structural metal ion essential for the structural integrity of the protein. In addition, NS3 interacts with another cofactor, NS4A, an accessory viral protein that induces a conformational change enhancing the hydrolytic activity. Biophysical studies on the isolated protease domain, whose behavior is similar to that of the full-length protein (e.g., catalytic activity, allosteric mechanism and susceptibility to inhibitors), suggest that a considerable global conformational change in the protein is coupled to zinc binding. Zinc binding to NS3 protease can be considered as a folding event, an extreme case of induced-fit binding. Therefore, NS3 protease is an intrinsically (partially) disordered protein with a complex conformational landscape due to its inherent plasticity and to the interaction with its different effectors. Here we summarize the results from a detailed biophysical characterization of this enzyme and present new experimental data.

19 July 2019 in Cancers
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ARAlberto Rodrigo
Alberto Rodrigo
JOJorge L. Ojeda
Jorge L. Ojeda
SVSonia Vega
Sonia Vega
OSOscar Sanchez-Gracia
Oscar Sanchez-Gracia
ALAngel Lanas
Angel Lanas
Olga AbianOlga Abian
Olga Abian
Risk population screening programs are instrumental for advancing cancer management and reducing economic costs of therapeutic interventions and the burden of the disease, as well as increasing the survival rate and improving the quality of life for cancer patients. Lung cancer, with high incidence and mortality rates, is not excluded from this situation. The success of screening programs relies on many factors, with some of them being the appropriate definition of the risk population and the implementation of detection techniques with an optimal discrimination power and strong patient adherence. Liquid biopsy based on serum or plasma detection of circulating tumor cells or DNA/RNA is increasingly employed nowadays, but certain limitations constrain its wide application. In this work, we present a new implementation of thermal liquid biopsy (TLB) for lung cancer patients. TLB provides a prediction score based on the ability to detect plasma/serum proteome alterations through calorimetric thermograms that strongly correlates with the presence of lung cancer disease (91% accuracy rate, 90% sensitivity, 92% specificity, diagnostic odds ratio 104). TLB is a quick, minimally-invasive, low-risk technique that can be applied in clinical practice for evidencing lung cancer, and it can be used in screening and monitoring actions.

6 November 2003
Verified
Journal Article
Closed access
AVAdrian Velazquez-Campoy
Adrian Velazquez-Campoy
SVSonia Vega
Sonia Vega
EFErin Fleming
Erin Fleming
UBUsman Bacha
Usman Bacha
Yasien SayedYasien Sayed
Yasien Sayed
EFErnesto Freire
Ernesto Freire