Professor of Biophysics


Our research

In the last 15 years our research has been focused on the development of methods of characterising the structure, dynamics and interactions of proteins in previously inaccessible states. These methods are based on the use of experimental data, in particular from nuclear magnetic resonance spectroscopy, as structural restraints in molecular dynamics simulations. Through this approach it is possible to obtain information about a variety of protein conformations, as for example those populated during the folding process, and about protein interactions in complex environments, including those generating aggregate species that are associated with neurodegenerative disorders such as Alzheimer's and Parkinson's diseases.

Application to neurodegenerative diseases

More recently, these studies have led us to investigate the physico-chemical principles of proteins homeostasis and their application to the development of therapeutic strategies against neurodegenerative diseases. Starting from the observation that proteins are expressed in the cell at levels close to their solubility limits, we are developing approaches to prevent or delay misfolding disorders based on the enhancement of our quality control mechanisms against protein aggregation.

Watch Professor Vendruscolo discuss his research

Take a tour of the Una Finlay Laboratory in the Centre for Misfolding Diseases

Publications

The αC-β4 loop controls the allosteric cooperativity between nucleotide and substrate in the catalytic subunit of protein kinase A
C Olivieri, Y Wang, C Walker, MV Subrahmanian, KN Ha, D Bernlohr, J Gao, C Camilloni, M Vendruscolo, SS Taylor, G Veglia
eLife
(2024)
12
Identification of high-affinity secondary nucleation inhibitors of Aβ42 aggregation from an ultra-large chemical library using Deep Docking
M Vendruscolo, M Brezinova, ZF Brotzakis, R Horne, VR Chowdhury, R Gregory, F Gentile
(2024)
Aggregate-binding aptamers for Parkinson's disease diagnostics
M Nowinska, J Chovas, M Donde, M Canzano, M Vendruscolo
FEBS OPEN BIO
(2024)
14
Optimizing performance characteristics of antibodies for single-molecule quantitative bioimaging
JC Breiter, C Loiseau, JS Beckwith, R Andrews, B Fu, PJ Magill, SF Lee, M Vendruscolo
FEBS OPEN BIO
(2024)
14
Kinetics and thermodynamics characterization of serum amyloid A (SAA) protein
H Nadwa, A Santucci, D Braconi, F Brotzakis, M Vendruscolo
FEBS OPEN BIO
(2024)
14
Secondary pathways cause the proliferation of amyloid aggregates of medin, an aortic medial amyloid peptide associated with cerebral amyloid angiopathy
VR Chowdhury, RI Horne, AG Diaz, M Vendruscolo
FEBS OPEN BIO
(2024)
14
Effects of aminosterols and berberine on the structural and dynamical properties of biological membranes against the action of misfolded protein oligomers
S Errico, G Lucchesi, D Odino, R Cascella, C Capitini, M Vendruscolo, M Zasloff, F Chiti
FEBS OPEN BIO
(2024)
14
The diversity of SNCA transcripts in neurons, and its impact on antisense oligonucleotide therapeutics
JR Evans, EK Gustavsson, I Doykov, D Murphy, GS Virdi, J Lachica, A Röntgen, MH Murtada, CW Pang, H Macpherson, AI Wernick, CE Toomey, D Athauda, ML Choi, J Hardy, NW Wood, M Vendruscolo, K Mills, W Heywood, M Ryten, S Gandhi
(2024)
Pharmacological inhibition of α-synuclein aggregation within liquid condensates.
ST Dada, Z Toprakcioglu, MP Cali, A Röntgen, MC Hardenberg, OM Morris, LK Mrugalla, TPJ Knowles, M Vendruscolo
Nature Communications
(2024)
15
Effects of α-synuclein proteoforms on the liquid-liquid phase separation and aggregation of α-synuclein
A Rontgen, Z Toprakcioglu, S Dada, O Morris, M Vendruscolo
FEBS OPEN BIO
(2024)
14

Co-Director

Research Interest Groups

Telephone number

01223 763873

Email address