Dr. Vasa Radonic  
Project coordinator

vasarad@biosense.rs

Location:
BioSense Institute, University of Novi Sad
Dr. Zorana Đinđića 1, 21000 Novi Sad, Serbia

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Presenters

Dr. Hajnalka Jankovics

Senior research fellow, leader of the Bio-Nanosystems Laboratory, at the Research Institute of Biomolecular and Chemical Engineering, Faculty of Engineering, University of Pannonia, Hungary

Hajnalka Jankovics received her PhD degree from the University of Szeged (SZTE), Hungary in 2003 on the field of solution chemistry and solid synthesis of the complexes of organotin(IV) cations and biologically relevant ligands. As a Marie Curie Postdoctoral Fellow at Technical University of Denmark, she extended her scientific experience with recombinant DNA technology techniques, protein expression and purification and the synthesis of artificial metalloproteins. After returning to SZTE she took part in the establishment of a new molecular biology research laboratory. She has been working in the Bio-Nanosystems Laboratory (Research Institute of Biomolecular and Chemical Engineering, University of Pannonia, Veszprém, Hungary) since 2008. Currently she is the leader of the research group and among others works on selecting or engineering and study of flagellin-based polymerizable binding proteins and the development of immobilizable enzymes and specific binder proteins for diagnostic applications or environmental detection.

Talk Title: A self-assembling protein for versatile biosensing applications

Bacterial flagellin, a key protein in the locomotor system of the organism, is a protein that can self-assemble and polymerize in vitro. Distinct parts of flagellin are responsible for its polymerization ability, and the D3 domain, the surface part of the long filaments it forms, can be genetically engineered to be versatile without compromising its self-assembling ability. By modifying or substituting the D3 domain, variants with binding, enzymatic activity or signaling properties can be developed. These can be used to build multifunctional mixed or block polymers under in vitro conditions, with up to tens of thousands of sensing units on their surface, resulting in excellent signal amplification in biosensing. In addition, flagellin variants can be incorporated into the filaments to provide both anchoring to the sensor surface and stabilization of the filaments by cross-linking. This strategy makes biosensors functionalized with sensing flagellar filaments superior to other protein (e.g. antibody)-based biosensors. Furthermore, as the D3 domain has a stable structure on its own, it is a suitable scaffold protein for directed evolutionary processes that can respond efficiently and rapidly to sensor development for the detection of emerging contaminants.

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This project is funded by the European Union under Horizon Europe GA 101159710