Konstanty Cieśliński

ORCID: 0000-0002-3504-1772
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About
Contact & Profiles
Research Areas
  • Microtubule and mitosis dynamics
  • Advanced Fluorescence Microscopy Techniques
  • Advanced Electron Microscopy Techniques and Applications
  • Photosynthetic Processes and Mechanisms
  • Protist diversity and phylogeny
  • RNA Research and Splicing
  • Nuclear Structure and Function
  • Monoclonal and Polyclonal Antibodies Research
  • Synthesis and Biological Evaluation
  • Bacteriophages and microbial interactions
  • Plant nutrient uptake and metabolism
  • Supramolecular Self-Assembly in Materials
  • Molecular Biology Techniques and Applications
  • Radiopharmaceutical Chemistry and Applications

European Molecular Biology Laboratory
2021-2023

DKFZ-ZMBH Alliance
2023

German Cancer Research Center
2023

Heidelberg University
2021

European Molecular Biology Organization
2019

European Molecular Biology Laboratory
2014-2017

Human chromosomes are captured along microtubule walls (lateral attachment) and then tethered to microtubule-ends (end-on through a multi-step end-on conversion process. Upstream regulators that orchestrate this remarkable change in the plane of kinetochore-microtubule attachment human cells not known. By tracking kinetochore movements using markers specific status, we reveal spatially defined role for Aurora-B kinase retarding To understand how activity is counteracted, compare roles two...

10.1038/s41467-017-00209-z article EN cc-by Nature Communications 2017-07-21

Proper chromosome segregation is crucial for cell division. In eukaryotes, this achieved by the kinetochore, an evolutionarily conserved multiprotein complex that physically links DNA to spindle microtubules and takes active role in monitoring correcting erroneous spindle–chromosome attachments. Our mechanistic understanding of these functions how they ensure error-free outcome mitosis still limited, partly because we lack a complete kinetochore structure cell. study, use single-molecule...

10.1083/jcb.202209094 article EN cc-by The Journal of Cell Biology 2023-01-27

Abstract Quantitative fluorescence and superresolution microscopy are often limited by insufficient data quality or artifacts. In this context, it is essential to have biologically relevant control samples benchmark optimize the of microscopes, labels imaging conditions. Here we exploit stereotypic arrangement proteins in nuclear pore complex as situ reference structures characterize performance a variety modalities. We created four genome edited cell lines which endogenously labeled...

10.1101/582668 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-03-20

Abstract Proper chromosome segregation is crucial for cell division. In eukaryotes, this achieved by the kinetochore, an evolutionarily conserved multi-protein complex that physically links DNA to spindle microtubules and takes active role in monitoring correcting erroneous spindle-chromosome attachments. Our mechanistic understanding of these functions how they ensure error-free outcome mitosis still limited, partly because we lack a comprehensive kinetochore structure cell. study, use...

10.1101/2021.12.01.469648 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2021-12-01
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