4.1.12 Biophysics


Profile of the graduate (in Slovak)

The graduate of the study program Biophysics is proficient in scientific methods of biophysics and can apply them in a creative way to solve a wide range of problems in the field of life sciences (physiology, molecular biology, biochemistry, pharmacology and theoretical medicine, theoretical biology and medicine, immunology, bioinformatics). The graduate is familiar with the methods of state-of-the-art interdisciplinary sciences in the field of biology, nanotechnology, and bioinformatics technologies, as well as their practical application. The graduate scientifically investigates and brings original solutions of problems and has actively acquired research methodology, scientific formulation of the problem, publication of scientific results and their presentation at professional events.

Regulations for doctoral studies at UPJŠ (in Slovak)
Study program (in Slovak)
Allocation of credits at UPJŠ (in Slovak)


Chief Guarantor Ing. Alexandra Zahradníková, DrSc.
Co-Guarantors Mgr. Marta Gaburjáková, PhD.
RNDr. Ivan Zahradník, CSc.


Mgr. Jana Gaburjáková, PhD.
doc. RNDr. Ľubica Lacinová, DrSc.
RNDr. Michal Cagalinec, PhD
RNDr. Alexandra Zahradníková, PhD.
Mgr. Vladimír Leksa, PhD., Ústav molekulárnej biológie SAV
RNDr. Karol Ondriaš, DrSc., Ústav klinického a translačného výskumu, BMC SAV

Entrance exams for the academic year 2016/17 were held on 16. 6. 2016 at 10:00 AM. in boardroom of DMCR IMPG SAS

Dissertation topics – akademic year 2016/2017:


Site: Department of Muscle Cell Research
Institute of Molecular Physiology and Genetics SAS
Topic: Local aspects of calcium feedback in excitation-contraction coupling.
Supervisor: RNDr. Alexandra Zahradníková, PhD. saschia.zahradnikova@savba.sk


Feedback in calcium signaling during excitation-contraction coupling regulates calcium homeostasis in heart muscle cells, action potential duration, and rate of membrane repolarization, which affects occurence of early afterdepolarizations. The aim of the work is to monitor the impact of local calcium release on the course of inactivation of calcium current, and changes in the molecular complex responsible for feedback that occur during postnatal development and physiological and pathological cardiac hypertrophy. The main methods are patch-clamp in combination with confocal mikroskopy, qPCR and Western blot to determine the expression of the protein and immunofluorescent staining of proteins of the dyadic complex.

Site: Department of Muscle Cell Research
Institute of Molecular Physiology and Genetics SAS
Topic: Study of morphological changes in Wolfram syndrome using super-resolution microscopy.
Supervisor: RNDr. Michal Cagalinec, PhD. michal.cagalinec@et.ee


Wolfram syndrome (WS) is a disease caused by a mutation of the WFS1 gene. WFS1 is expressed at high levels in brain and heart, and is localized in the membrane of endoplasmic reticulum (ER) where it modulates the level of calcium and ER stress. In addition, typical WS symptoms are symptoms of mitochondrial disease. The aim of this project is therefore to clarify whether in rats  with deletion of the WFS1 gene there are ultrastructural changes in cardiac cells to be detected by super-resolution microscopy  as an alternative to electron microscopy techniques.

Site: Department of Cell Physiology and Genetics
Institute of Molecular Physiology and Genetics SAS
Topic: Calcium regulation of the cardiac ryanodine receptor.
Supervisor: Mgr. Marta Gaburjáková, PhD. marta.gaburjakova@savba.sk
Supervisor-specialist: Mgr. Jana Gaburjáková, PhD. jana.gaburjakova@savba.sk


Contraction of cardiac muscle cells occurs after massive release of Ca2+ from the sarcoplasmic reticulum cisternae through activated ryanodine receptors (RYR2s) operating as Ca2+ channels. The main physiological activator of RYR2 channels is cytosolic Ca2+, which binds to the voluminous cytosolic domain. An important role is played by luminal regulation mediated by binding of Ca2+ to the small luminal portion of the RYR2 channel. At present, intensive search for the binding sites on the Ca2+ channel,  and the aim of the study will be to acquire new knowledge of the localization of these physiologically important regulatory sites. To achieve the objectives PhD. work  electrophysiological experiments at the level of single RYR2 channels will be performed in combination with spectroscopic, biochemical and bioinformatics methods.