Herwig Schüler

Herwig Schüler

Senior lecturer

Personal profile

Research

My research revolves around ADP-ribosyltransferases, which cleave NAD+ to link ADP-ribose to their targets - proteins or nucleic acids. This flags target proteins for specific activities in our cells. A number of human enzymes, the PARP enzymes, catalyze this reaction. PARP enzymes are drug targets: Drugs that inhibit PARP activity are already in use today in treatment of certain forms of cancer. We want to understand enzymatic mechanisms and improve the fit of PARP inhibitors to their enzymatic pockets. This will lead to more potent, more selective drugs in the future. Many bacterial toxins, produced by pathogenic bacteria, have the same activity. We strive to contribute to a better understanding of these toxins and to create inhibitors also for their activities, with the aim of creating new anti-infective drugs.

PhD students

Carmen Ebenwaldner

Constantinos Chatzicharalampous

BSc/MSc students

Herman Sjölin

Ikechukwu Casmir

Ljubomir Grcic

Alumni

Archimede Torretta (postdoc)

Angelica Nash (BSc)

Anton Hansson (BSc)

Antonio Ginés Garcia Saura (postdoc)

Elin Olsson (BSc)

Hannah Olsson (BSc)

Mathieu Long (postdoc)

Moa Rundberg (BSc)

Noah Björklöf Dolan (BSc)

Virginia Cristobal Martin (BSc)

Teaching

KEMA03/KEMA13 - Biochemistry, basic course (course responsibility)

MOBA02 - Chemistry of the cell (course responsibility)

KEMC03 - Experimental protein chemistry (lecturer)

KEML10, KEMR30 - Project work on Bachelor and Masters level

Societal impact

Expertise related to UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  • SDG 3 - Good Health and Well-being

UKÄ subject classification

  • Biochemistry and Molecular Biology
  • Structural Biology
  • Biophysics
  • Medicinal Chemistry

Free keywords

  • ADP-ribosylation
  • bacterial toxins
  • drug development
  • enzyme mechanism
  • protein structure
  • protein complexes

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Collaborations the last five years

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