CRISPR/Cas9

Data science has long been part of our research – including artificial intelligence. However, AI has also permeated the daily lives of many people. At "Insights," we were curious: What books would ChatGPT & Co. recommend for laypeople interested in molecular medicine? The result: three bestsellers.

Sarah Hedtrich heads a guest group at the Max Delbrück Center. The Johanna Quandt Professor at the Berlin Institute of Health at Charité (BIH) is working on organ-on-a-chip models to develop new treatment options for rare hereditary and inflammatory skin and lung diseases.

The Max Delbrück Center is a partner of the doctoral network GetRadi, which was started in September. Young scientists who want to learn how to develop gene therapies for rare diseases can apply to be a part of the EU-funded project until October 20.

Klaus Rajewsky’s life reads like a chronicle of immunogenetics. He grasped the opportunities offered by radical changes in molecular biology. He established standard methods for researching gene functions and diseases like cancer. And he continues to contribute to our understanding of antibody-producing B cells.

MyoPax, a new spin-off of the Max Delbrück Center and Charité, receives a 1.3 million euros loan to jump-start its entrepreneurial activities. The start-up develops regenerative therapies for previously incurable muscle diseases using its innovative muscle stem cell technology.

A CRISPR-based rapid test called CrisprZyme could help general practitioners to diagnose heart attacks and distinguish between different types of prostate cancer. They do not even need a lab, as an international team of scientists – including Michael Kaminski – reports in "Nature Nanotechnology".

The molecular tool CRISPR-Cas9 can be used to treat inherited blood disorders, but this may cause unintended genetic alterations. A team led by MDC researchers Klaus Rajewsky and Van Trung Chu has now presented an approach in “Science Advances” that minimizes such adverse consequences.

Medical interventions in the human body can prolong our lives. But where do we draw the line? Questions like these were the subject of the Salon Sophie Charlotte "Still, Life is Life" of the Berlin-Brandenburg Academy of Sciences and Humanities. The MDC was part of it.

There’s likely to be a fundamental difference between how a medical practicioner and an artist view genetic editing with CRISPR. But both perspectives reveal possible ways to shape life in nature. Science meets art: the Max Delbrück Center at the Salon Sophie Charlotte 2022 in Berlin.

Mutations that lead to muscle atrophy can be repaired with the gene editor CRISPR-Cas9. A team led by ECRC researcher Helena Escobar has now introduced the tool into human muscle stem cells for the first time using mRNA, thus discovering a method suitable for therapeutic applications.