Márta Kotormán

Dr. Márta Kotormán


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2004 in Biochemical and Biophysical Research Communications
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Journal Article
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LSL.M Simon
L.M Simon
MKMárta Kotormán
Márta Kotormán
ASAndras Szabo
Andras Szabo
Győző GarabGyőző Garab
Győző Garab
ILI Laczkó
I Laczkó

1 July 2006 in Journal of Molecular Catalysis B: Enzymatic
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Journal Article
Closed access
ASAndras Szabo
Andras Szabo
MKMárta Kotormán
Márta Kotormán
ILIlona Laczkó
Ilona Laczkó
LSL. Mária Simon
L. Mária Simon

10 May 2017 in Protein & Peptide Letters
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Journal Article
Open access
MKMárta Kotormán
Márta Kotormán
PKPhanindra B. Kasi
Phanindra B. Kasi
LHLaszlo Halasz
Laszlo Halasz
Attila BoricsAttila Borics
Attila Borics
The aim of the present study was to examine the potential role and applicability of dietary supplements in reducing the risk of development of amyloid diseases associated with the gastrointestinal tract, such as type II diabetes. Trypsin, a well-known serine protease was used as a model protein in our experiments. The effect of various red wines on the formation of amyloid-like fibrils of trypsin was studied in vitro, in aqueous ethanol, at pH 7.0. Turbidity measurements, aggregation kinetics experiments, Congo red binding assays and electronic circular dichroism spectroscopic measurements were used to follow the aggregation process in the presence or absence of various red wines. The results suggest that red wines effectively inhibit the formation of amyloid-like fibrils of trypsin and the inhibitory effect is dose-dependent. The extent of inhibition was found to be proportional to the total concentration of phenolic compounds.

2 November 2015 in Protein & Peptide Letters
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Journal Article
Closed access
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MKMárta Kotormán
Márta Kotormán
LSL. Mária Simon
L. Mária Simon
Attila BoricsAttila Borics
Attila Borics
MSMárton Richárd Szabó
Márton Richárd Szabó
KSKitti Szabó
Kitti Szabó
LFLivia Fülop
Livia Fülop
Abstract: The formation of amyloid-like fibrils was studied by using the well-known serine protease trypsin as a model protein in the presence of ethanol as organic solvent. Trypsin forms amyloid-like fibrils in aqueous ethanol at pH = 7.0. The dye Congo red (CR) was used to detect the presence of amyloid-like fibrils in the samples. The binding of CR to fibrils led to an increase in absorption intensity and a red shift in the absorption band of CR. Thioflavin T (ThT) and 8-anilino-1- naphthalenesulfonic acid (ANS) binding assays were employed to characterize amyloid-like fibril formation. The ThT binding assay revealed that the protein exhibited maximum aggregation in 60% (v/v) ethanol after incubation for 24 h at 24 oC. The ANS binding results indicated that the hydrophobic residues were more exposed to the solvent in the aggregated form of the protein. The effects of polyethylene glycol (PEG) on the formation of amyloid-like fibrils was studied in vitro. The aggregation of trypsin was followed via the kinetics of aggregation, the far-UV circular dichroism (CD) and transmission electron microscopy (TEM) in the presence and absence of PEG. The CD measurements indicated that the protein aggregates have a cross-beta structure in 60% ethanol. TEM revealed that trypsin forms fibrils with a thread-like structure. The inhibitory effect of PEG on the aggregation of trypsin increased with rising PEG concentration. PEG therefore inhibits the formation of amyloid-like fibrils of trypsin in aqueous ethanol.

1 December 2018 in Acta Biologica Hungarica
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Journal Article
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MKMárta Kotormán
Márta Kotormán
AVAlexandra Varga
Alexandra Varga
PKPhanindra Babu Kasi
Phanindra Babu Kasi
JNJános Nemcsók
János Nemcsók
During the study of inhibition of amyloid fibril formation, α-chymotrypsin protein was developed in 55% ethanol at pH 7.0. We investigated the inhibitory effect of different spices on amyloid fibril formation using turbidity measurements and Congo red binding assays. We found that all spices except the black pepper and caraway seed prevented fibril formation. The highest inhibition was measured with the clove, which reduced the amount of aggregates by 90%. We studied the inhibitory effect of the cloves at different concentrations on aggregation, it was found that the inhibitory activity of clove is dependent on concentration. We have measured the total phenolic content of the spice extracts too. Based on all these findings we have come to the following conclusion: Our results indicate that spices can contain other compounds too – not only phenolic compounds – which influence the formation of amyloid fibrils, and the effectiveness of various phenolic compounds are different.

1 June 2018 in Acta Biologica Hungarica
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Journal Article
Closed access
MKMárta Kotormán
Márta Kotormán
ZKZita Kelemen
Zita Kelemen
PKPhanindra Babu Kasi
Phanindra Babu Kasi
JNJános Nemcsók
János Nemcsók
We tested the amyloid fibril formation inhibitory effect of seven teas diluted in 55% ethanol at pH 7.0 at a protein concentration of 0.15 mg/ml α-chymotrypsin. In the experiments we investigated the formation and inhibition of amyloid fibrils by turbidity measurements, aggregation kinetics experiments and Congo red binding assay. The results suggest that the different teas effectively inhibit the formation of amyloidlike fibrils. The two most potent inhibitors were peppermint and melilot, extracts which almost completely inhibited the formation of aggregates in 5-fold dilution. The inhibitory effect on the aggregation formation of melilot and peppermint extracts was concentration dependant. The extent of inhibition was found to be proportional with the total concentration of phenolic compounds.