Advancing Synthethic Supramolecular chemical biology

Informacje na temat projektu

ASSEMBLY

Identyfikator umowy o grant: 844872

DOI

10.3030/844872

Realizacja projektu zakończyła się 30 Września 2021

Data podpisania przez KE 11 Kwietnia 2019

Data rozpoczęcia 1 Sierpnia 2019

Data zakończenia 23 Grudnia 2021

Finansowanie w ramach

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Koszt całkowity

€ 175 572,48

Wkład UE

€ 175 572,48

Koordynowany przez

TECHNISCHE UNIVERSITEIT EINDHOVEN
Netherlands

Periodic Reporting for period 1 - ASSEMBLY (Advancing Synthethic Supramolecular chemical biology)

Okres sprawozdawczy: 2019-08-01 do 2021-07-31

Podsumowanie kontekstu i ogólnych celów projektu

The use of cucurbituril as supramolecular tool to develop novel chemical biologically relevant interactions was explored. More robuust and elaborate systems are essential for the development of personalized medicine, advancement of the field of biosensors and development of more complex Logic gates and molecular diagnostics.

To start to tackle these issues a better understanding signaling networks is required. Split proteins offer great advantages when designing supramolecular synthetic signalling networks. When combined with our cucurbituril-bases molecular recognition system they have great promise to function in parallel with any natural signalling systems, thus having the potential to limit its biological interference, while still effecting the desired interactions.

Prace wykonane od początku projektu do końca okresu sprawozdawczego oraz najważniejsze dotychczasowe rezultaty

By attaching cucurbituril-selective guests to the novel split luciferase NanoLuc a powerful tool was created for signal readout allowing of finetuning of the ongoing interactions. To increase the stability of the system over time and to mitigate substrate depletion a secondary ratiometric system was developed that allows for a direct and fair calibration in the system, using the Nanoluc-mNeonGreen BRET pair.

The formed supramolecular assembly between the cucurbituril and its guests can be modulated via competitor systems. The development of a light-sensitive peptidic inhibitor allows for the direct assembly of the splitprotein-cucurbituril complex in the aqueous media. Additionally a light-sensitive peptidic inhibitor was developed that, after being exposed to light facilitated the direct, irreversible de-assembly of the reformed splitprotein-cucurbituril complex in aqueous media.

To increase the understanding of the multi-complex equilibria that are formed in the model systems, the use of computational modeling proved valuable. However, as every system is different it was found time-consuming to have to develop and mathematically derive all the elaborate thermodynamic equations by hand. To facilitate this, the error prone method was replaced by an automated derivitization process. The model builder program was designed to be easy to use and modular. Stress tests show that the novel developed algorithm can cope with very large multi-component complexes with ease.

Innowacyjność oraz oczekiwany potencjalny wpływ (w tym dotychczasowe znaczenie społeczno-gospodarcze i szersze implikacje społeczne projektu)

The manuscript for the development of the cucurbituril-controlled the split nanoluciferase with the ratiometric calibrator with competitor controlled modulation is under construction. This project offers a reliable and robuust system that can be implemented in synthetic signalling systems, biosensors.
The manuscript detailing the novel approach to construct computational models based on multi-component complex equilibria is currently under review. The program is already been shared and tested by different research groups within the department and has been useful in the creation of several models. The developed models help provide key insights into the molecular mechanisms that are underlying many of the processes that are studied in the department. As soon as the project clear review and the full program and coding will be publicly available.

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