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Genetic Code Expansion for Studying Posttranslational Modifications
Last Updated: 2026-02-05 16:30:52
Abstract
In this block course we will prepare proteins bearing site-specifically installed post-translational modifications using genetic code expansion. The impact of the post-translational modifications on enzymatic activity and protein-protein interactions will be studied.
Objective
Students will learn basic techniques for genetic code expansion. They will learn how to synthesize non-canonical amino acids (ncAAs), manipulate plasmids through cloning techniques to introduce an amber codon at a user defined site in a gene of interest, express and purify recombinant proteins bearing site-specific ncAAs using state-of-the-art chromatographic techniques, characterize the target protein using mass spectrometry and analyze the properties of the target protein regarding enzymatic activity and protein-protein interactions using biophysical techniques. After the course, participants should be able to apply the gained skills in future chemical and molecular biology lab courses and projects. Individual reports describing the experiments and obtained results must be prepared by the end of the course. At the end of the course, each team (consisting of two participants each) will present their results in an oral presentation.
Content
During this block course, the participants will study the impact of different post-translational modifications (PTMs) on protein function using genetic code expansion. The participants will work in teams of two, will first synthesize different ncAAs mimicking PTMs, such as acylated lysine derivates (e.g. acetlylysine, butryllysine etc.). These ncAAs will be incorporated into target proteins using orthogonal aminoacyl tRNA synthetase / tRNA pairs, which direct the site-specific incorporation in response to an in frame introduced amber stop codon (amber suppression). Therefore, the participants will introduce the amber stop codon at different positions in the gene of interest using standard molecular cloning techniques. After recombinant expression of the target protein, the participants will isolate the ncAA-bearing target proteins using different chromatography techniques using a FPLC system. After characterization of the PTM-bearing protein using mass spectrometry, the participants will study the impact of the PTM on enzymatic activity and protein-protein interactions using biophysical techniques.
Resources
Lecture Notes
All the required theoretical and experimental informations can be found in the provided script. Details will be discussed in class. Relevant research papers will be recommended for reading during the seminars.
General Information
- Language
- English
- Levels
- BSC
- Frequency
- Yearly recurring
Examination
- Type
- graded semester performance
Course Components
| Type | Title | Time & Place | Hours |
|---|---|---|---|
| practical/laboratory course |
Genetic Code Expansion for Studying Posttranslational Modifications
Block course in the 2nd quarter of the autumn semester.
|
No time listed | 100 h semesterly |
Offered In
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Block Courses (Registration for Block courses is mandatory. Please register under . Registration period: from 22.07.2024 - 09.08.2024 Please note the ETH admission criteria for the admission of ETH students to ETH block courses on the block course registration website under "allocation".)
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Block Courses in 2nd Quarter of the Semester (From 10.10.2024 to 1.11.2024)
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Block Courses (Registration for Block courses is mandatory. Please register under . Registration period: from DATUM Please note the ETH admission criteria for the admission of ETH students to ETH block courses on the block course registration website under "allocation".)
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Block Courses in the 2nd Quarter of the Semester (Von 10.10.2024 bis 01.11.2024)
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