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Aggrescan3D (A3D) 2.0: prediction and engineering of protein solubility

Nucleic acids research, 2019-07, Vol.47 (W1), p.W300-W307

2019

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Development of the ATLAS Liquid Argon Calorimeter Readout Electronics for the HL-LHC

EPJ Web of Conferences, 2024, Vol.295, p.2010

2024

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Advances in the Prediction of Protein Aggregation Propensity

Current medicinal chemistry, 2019, Vol.26 (21), p.3911-3920

2019

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Editorial: Protein Solubility and Aggregation in Bacteria

Frontiers in microbiology, 2016-07, Vol.7, p.1178-1178

Ventura, Salvador

2016

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Design and redesign journey of a drug for transthyretin amyloidosis

Neural regeneration research, 2025-04, Vol.20 (4), p.1096-1097

2025

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AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides

BMC bioinformatics, 2007-02, Vol.8 (1), p.65-65, Article 65

2007

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Computational re-design of protein structures to improve solubility

Expert opinion on drug discovery, 2019-10, Vol.14 (10), p.1077-1088

2019

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AMYCO: evaluation of mutational impact on prion-like proteins aggregation propensity

BMC bioinformatics, 2019-01, Vol.20 (1), p.24-24, Article 24

2019

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α-Helical peptidic scaffolds to target α-synuclein toxic species with nanomolar affinity

Nature communications, 2021-06, Vol.12 (1), p.3752-14, Article 3752

2021

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What makes a protein sequence a prion?

PLoS computational biology, 2015-01, Vol.11 (1), p.e1004013-e1004013

2015

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Minimalist Prion-Inspired Polar Self-Assembling Peptides

ACS nano, 2018-06, Vol.12 (6), p.5394-5407

2018

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Functionalized Prion-Inspired Amyloids for Biosensor Applications

Biomacromolecules, 2021-07, Vol.22 (7), p.2822-2833

2021

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Editorial: Protein Aggregation and Solubility in Microorganisms (Archaea, Bacteria and Unicellular Eukaryotes): Implications and Applications

Frontiers in microbiology, 2020-11, Vol.11, p.620239-620239

2020

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Staphylococcal Bap Proteins Build Amyloid Scaffold Biofilm Matrices in Response to Environmental Signals

PLoS pathogens, 2016-06, Vol.12 (6), p.e1005711-e1005711

2016

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Specific Hsp100 Chaperones Determine the Fate of the First Enzyme of the Plastidial Isoprenoid Pathway for Either Refolding or Degradation by the Stromal Clp Protease in Arabidopsis

PLoS genetics, 2016-01, Vol.12 (1), p.e1005824

2016

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Fluorescent dye ProteoStat to detect and discriminate intracellular amyloid-like aggregates in Escherichia coli

Biotechnology journal, 2014-10, Vol.9 (10), p.1259-1266

2014

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Coiled-coil inspired functional inclusion bodies

Microbial cell factories, 2020-06, Vol.19 (1), p.117-16, Article 117

2020

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Tolcapone, a potent aggregation inhibitor for the treatment of familial leptomeningeal amyloidosis

The FEBS journal, 2021-01, Vol.288 (1), p.310-324

2021

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pH-Responsive Self-Assembly of Amyloid Fibrils for Dual Hydrolase-Oxidase Reactions

ACS catalysis, 2021-01, Vol.11 (2), p.595-607

2021

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Amyloidogenic regions and interaction surfaces overlap in globular proteins related to conformational diseases

PLoS computational biology, 2009-08, Vol.5 (8), p.e1000476

2009

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Cryo-EM structure of hnRNPDL-2 fibrils, a functional amyloid associated with limb-girdle muscular dystrophy D3

Nature communications, 2023-01, Vol.14 (1), p.239-12, Article 239

2023

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Repositioning tolcapone as a potent inhibitor of transthyretin amyloidogenesis and associated cellular toxicity

Nature communications, 2016-02, Vol.7 (1), p.10787-10787, Article 10787

2016

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C-mannosylation supports folding and enhances stability of thrombospondin repeats

eLife, 2019-12, Vol.8

2019

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In-Silico Analysis of pH-Dependent Liquid-Liquid Phase Separation in Intrinsically Disordered Proteins

Biomolecules (Basel, Switzerland), 2022-07, Vol.12 (7), p.974

2022

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Prion-like domain disease-causing mutations and misregulation of alternative splicing relevance in limb-girdle muscular dystrophy (LGMD) 1G

Neural regeneration research, 2020-12, Vol.15 (12), p.2239-2240

2020

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Aggrescan3D (A3D) 2.0: prediction and engineering of protein solubility

Development of the ATLAS Liquid Argon Calorimeter Readout Electronics for the HL-LHC

Advances in the Prediction of Protein Aggregation Propensity

Editorial: Protein Solubility and Aggregation in Bacteria

Design and redesign journey of a drug for transthyretin amyloidosis

AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptides

Computational re-design of protein structures to improve solubility

AMYCO: evaluation of mutational impact on prion-like proteins aggregation propensity

α-Helical peptidic scaffolds to target α-synuclein toxic species with nanomolar affinity

What makes a protein sequence a prion?

Minimalist Prion-Inspired Polar Self-Assembling Peptides

Functionalized Prion-Inspired Amyloids for Biosensor Applications

Editorial: Protein Aggregation and Solubility in Microorganisms (Archaea, Bacteria and Unicellular Eukaryotes): Implications and Applications

Staphylococcal Bap Proteins Build Amyloid Scaffold Biofilm Matrices in Response to Environmental Signals

Specific Hsp100 Chaperones Determine the Fate of the First Enzyme of the Plastidial Isoprenoid Pathway for Either Refolding or Degradation by the Stromal Clp Protease in Arabidopsis

Fluorescent dye ProteoStat to detect and discriminate intracellular amyloid-like aggregates in Escherichia coli

Coiled-coil inspired functional inclusion bodies

Tolcapone, a potent aggregation inhibitor for the treatment of familial leptomeningeal amyloidosis

pH-Responsive Self-Assembly of Amyloid Fibrils for Dual Hydrolase-Oxidase Reactions

Amyloidogenic regions and interaction surfaces overlap in globular proteins related to conformational diseases

Cryo-EM structure of hnRNPDL-2 fibrils, a functional amyloid associated with limb-girdle muscular dystrophy D3

Repositioning tolcapone as a potent inhibitor of transthyretin amyloidogenesis and associated cellular toxicity

C-mannosylation supports folding and enhances stability of thrombospondin repeats

In-Silico Analysis of pH-Dependent Liquid-Liquid Phase Separation in Intrinsically Disordered Proteins

Prion-like domain disease-causing mutations and misregulation of alternative splicing relevance in limb-girdle muscular dystrophy (LGMD) 1G

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