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Development of bioconjugates and modules for targeted treatment of high-mortality tumors

NVKP_16-1-2016-0036 Consortium Project

Head: László Kőhidai MD, PhD, Assoc. Professor

The main research topics of the Chemotaxis Research Group include:

(i) testing for cell adhesion, chemotaxis, and other cellular physiological effects;
(ii) analyzing signal phylogenesis in a ciliated model;
(iii) characterization 'Chemotaxome' as a novel concept of system biology.

It is also of great importance to contribute to the development of drug targeting conjugates (e.g. tumors, atherosclerosis).

The model cells of the experiments are unicellular (Tetrahymena pyriformis) and numerous mammalian tumor cell lines. The Research Group hosts the NKTH / NEKIFUT SKI Certified Impedance-Based Cellular Analysis Core Facility (ECIS / xCELLigence).

 

Today, oncology has become one of the leading causes of death in the world and in Hungary. Proper treatment is one of the most important strategic issues in health today. An important element of this new type of personalized therapy can be targeted tumor therapy, which can lead to improved life expectancy and quality of life for patients with high mortality and severe tumors, which of course has significant national economic benefits. In contrast, to the individual conjugates produced for this purpose by individual research teams working in the world, we aim to provide a 3-module library of compounds that allow multiple combinations of their individual elements to be easily adapted to individual tumor types. In doing so, a number of novel drugs, bifunctional linker molecules and peptide-based control molecules, will be chemically prepared and the biological activity of individual or combinations thereof will be investigated. Well-trained research staff (15-20 persons), high quality instrument pool (e.g. IR, NMR, HPLC-MS, RP-HPLC, peptide synthesizer, biological assay equipment, flow cytometer, microscopes, gel electrophoresis) , Western blot, RT-PCR) and an internationally recognized knowledge base on the subject. New applications (5-8 people) and new tools implemented within the project further increase the chances of effective implementation. Within 3 years, the number of compounds in the modules will be sufficient to produce from 50 to 100 new conjugates in combination, which may be capable of treating a broad spectrum of tumors. The individual compounds of the modules (intermediates) and the conjugates that can be made from them may, after appropriate patenting, become marketable products for researchers in the field or even for pharmaceutical companies. Potential revenues may also allow for continued expansion of compound stores.

 

 

       List of supported projects

Title                 (in Hungarian)

Type

Fund in ThHUF

 Period

Supervisor

Joint Researcher

Qalification

Hatóanyagot, epitopot illetve riporter molekulát tartalmazó peptid- és fehérjekonjugátumok szintézise, hatásvizsgálata

OTKA K 68285

20.000 eFt

2007-2011

 

Kőhidai L.

Active

The Integration of Biomolecular Motors for Bacterial Actuation, Sensing and Transport (BAST) at Micro/Nanoscale NSF (USA)

NSF CMMI-0745019

  2008-2010 Kim, MinJun Kőhidai L. Active

Epitópok illetve antimikrobiális hatású peptidek, peptidszármazékok célzott bevitele makrofág típusú sejtekbe.

OTKA T 43576

13.000 eFt

2003-2007

 

Kőhidai L.

Excellent

Kemotaktikus hatású SXWS peptid-család hatásvizsgálata egysejtű Tetrahymena és PMN-sejt modell-rendszerben. Receptor-evolúciós vizsgálatok.

OTKA T 032533

2680 eFt

2000-2004

Kőhidai L.

.

Good

Endogén citokinek vizsgálata a filogenezis korai szakaszát képviselő modellen.

OTKA T22754

2000eFt

1997-2002

Kőhidai L.

 

Good

Szignál-molekulák által kiváltott kemotaxis szelekciós hatásainak vizsgálata - Receptor-evolúciós és morfometriai aspektusok

OTKA

T17773

1.000

1994-1998

Kőhidai, L.

 

Adequate

Intracelluláris folyamatok nagyfelbontású video-mikroszkópos vizsgálóeljárásának továbbfejlesztése egysejtû és szövettenyészeti modellen

OTKA

1.000

1995-1996

 

Kőhidai L.

 

A kemotaktikus drug-targeting alkalmazása parodontitis prevenciójéában.

ETT-369

1.800

2006-2008

Kőhidai L.

 

Active

Új lehetőség a meddőség kezelésére: Szubletális stresszkezelt petesejtek…

JÁP

NKFP07_1-EGG_CARE-HU

45.000

2008-2010

Kőhidai L.

 

Active

Epitópok illetve antimikrobiális hatású peptidek, peptidszármazékok célzott bevitele makrofág típusú sejtekbe.

T43576

 

1300 eFt

 

2003-2006

 

 

Láng O.

Closed

 

 

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