Reaseach Group Dr. Christina Schüler

Dr. Christina Schüler

ORCID: 0000-0002-8694-1738

Curriculum Vitae

Since 2016   Junior Group Leader; Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences

2011-2016   Postdoctoral fellow in the lab of Prof. Dr. Alexander Gottschalk; Goethe University Frankfurt, Buchmann Institute for Molecular Life Sciences

2010-2011   Postdoctoral fellow in the lab of Joachim W. Deitmer; University of Kaiserslautern, Department of Biology, General Zoology and Cellular Neurobiology

2006-2010   PhD thesis: „Funktionelle Interaktion zwischen Carboanhydrasen und dem elektrogenen Natriumbikarbonat-Kotransporter NBCe1 - Untersuchungen im Xenopus-Oozyten-Expressionssystem“ in the lab of Joachim W. Deitmer; University of Kaiserslautern, Department of Biology, General Zoology and Cellular Neurobiology

2002-2006   Studies in Biology; University of Kaiserslautern

2001-2002   Technical Assistant; Boehringer Ingelheim Pharma KG

1998-2001   Vocational Training; Boehringer Ingelheim Pharma KG

Extracurricular Experience & Awards

2007-2010   Associated member of the Research Training Group GRK 845 ”Molecular, physiological and pharmacological analysis of cellular membrane transport“

2007   Award of the ”Freundeskreis der Universität Kaiserslautern e.V.“ for the diploma thesis

 

Projects:

Characterization of catecholaminergic polymorphic ventricular tachycardia (CPVT) mutations and specific drug screen in the pharynx of C. elegans as an optogenetic arrhythmia model

CPVT is an inherited disturbance of the heart rhythm (arrhythmia) that is induced by stress, or that occurs during exercise. If untreated, CPVT is highly lethal. It often remains unnoticed, due to normal baseline electrocardiograms. Most mutations that have been linked to CPVT are found in two genes, i.e. ryanodine receptor 2 (RyR2) and calsequestrin 2 (CASQ2), two proteins fundamentally involved in the regulation of intracellular Ca2+ in cardiac myocytes. Many different (>170) CPVT mutations and polymorphisms are known. We inserted several CPVT mutations into C. elegans genes unc-68 (RyR) and csq-1 (CASQ) and crossed them with our strain expressing ChR2 in pharyngeal muscle cells to allow an optogenetic stimulation. We characterize those CPVT mutations by electrophysiology and calcium imaging, and perform drug tests with a screening platform to identify candidates for a patient-specific treatment.

Employees:

Marcial Engel – PhD student

Yves Wörmann – student worker

Hanna Kaestner – student worker

Alumnis:

Paula Dyck

Bojana Languille

Caroline Kollmannsperger

Dana Maureen Hebchen

Franziska Hannig