Krzysztof Mikołajczyk

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Assistant professor

Ludwik Hirszfeld Institute of Immunology and Experimental Therapy

Poland

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About

Dr. Krzysztof Mikołajczyk is an Assistant Professor at the Ludwik Hirszfeld Institute of Immunology and Experimental Therapy in Poland. His research focuses on glycosylation processes and the interactions between glycoproteins and pathogens, as demonstrated in his recent publications. He actively explores the roles of glycosyltransferases and the mechanisms by which pathogens exploit glycosphingolipids. Additionally, his work includes the study of glycoengineered cell models and their applications in understanding Shiga toxin receptors.

Recent Grants

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Exploring the binding differences of Shiga toxins to CHO-Lec2 and HEK293T cells.

Open Date: 2023-11-01

Close Date: 2023-11-01

Grant: Close

Rola dimeryzacji glikozylotransferaz w wiązaniu toksyn Shiga do glikosfingolipidowych i glikoproteinowych receptorów.

Open Date: 2022-01-01

Close Date: 2025-01-01

Grant: Close

Ludzka syntaza Gb3/CD77: czy N-glikany mogą wpływać na syntezę glikosfingolidów?

Open Date: 2017-09-07

Close Date: 2020-09-06

Articles (13)

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2025

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2021

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POLAND

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Katarzyna Kapczyńska

Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences

POLAND

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Jolanta Lukasiewicz

Head

Ludwik Hirszfeld Institute of Immunology and Experimental Therapy

POLAND

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Krzysztof Mikołajczyk

Research Interests

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Recent Grants

Articles (13)

Expression of a human Gb3/CD77 synthase in insect and human cells: comparison of activity and glycosylation

Phage receptor binding protein and Fc fragment fusion enhances phagocytosis of Y. enterocolitica

Glycoproteins, Glycolipids, or Both: Why do Glycosyltransferases Recognize Different Acceptors?

B4GALT5-deficient CHO-Lec2 cells expressing human α1,4-galactosyltransferase: A glycoengineered cell model for studying Shiga toxin receptors

Delving into human α1,4-galactosyltransferase acceptor specificity: The role of enzyme dimerization

Gb3 trisaccharide-bearing exosomes as a novel neutralizer for Shiga toxin type 1

One of the two N-glycans on the human Gb3/CD77 synthase is essential for its activity and allosterically regulates its function

Microbial lectome versus host glycolipidome: How pathogens exploit glycosphingolipids to invade, dupe or kill

Sialic Acids as Receptors for Pathogens

Missing the sweet spot: one of the two N-glycans on human Gb3/CD77 synthase is expendable

Human Gb3/CD77 synthase produces P1 glycotope-capped N-glycans, which mediate Shiga toxin 1 but not Shiga toxin 2 cell entry

Two paralogous gb3/cd77 synthases in birds show different preferences for their glycoprotein and glycosphingolipid substrates

How glycosylation affects glycosylation: the role of N-glycans in glycosyltransferase activity

Collaborators (8)

Lukasz Sobala

Marcin Czerwinski

Sebastian Kmiecik

Edyta Majorczyk

Mariusz Olczak

Katarzyna Haczkiewicz-Leśniak

Katarzyna Kapczyńska

Jolanta Lukasiewicz

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