VVZ API is not affiliated with ETH Zurich. Data might be outdated or incorrect. Please view the official ETHZ Vorlesungsverzeichnis for binding information.
Cryo-Electron Microscopic Studies of Ribosomal Complexes with Biomedically Important Viral Proteins
Last Updated: 2026-02-05 16:38:43
Abstract
Many viruses have evolved specialized mechanisms to hijack the host gene expression machinery and employ cellular resources to regulate viral life cycle. They accomplish this through producing non-structural proteins that can, among other things, inhibit host protein synthesis. Participants of this course will visualize ribosomes in complex with a non-structural viral protein at high resolution.
Objective
The goal of the course is to acquire the most important techniques and methods for the purification and structural characterisation of macromolecular complexes by transmission electron microscopy. The emphasis of the course is on the special practical requirements for the application of these techniques on macromolecular structures in the MDa range.
Content
Protein synthesis is a very energy intensive process that can consume over half the total metabolism of a cell. In eukaryotes, translation is therefore tightly regulated at the stage of initiation. Regulatory processes are much more complex at this step than in prokaryotes and a large number of RNA modification processes and translation initiation factors are required to ensure faithful initiation, elongation and termination of translation. However, several viruses may interfere with host translation by affecting the initiation step or by modifying the activity of key initiation factors to ensure an efficient translation of viral mRNA. Amongst such viruses is also SARS-CoV-2, which infects a large variety of vertebrate species. On entering host cells, the viral genomic RNA is translated by the cellular protein synthesis machinery to produce a set of non-structural proteins, which by inhibiting host translation render cell conditions favorable for viral production. Within the Ban lab, we have studied, and continue to investigate, medically relevant viral proteins. This course will involve producing and attempting to determine the structure of a non-structural viral protein in a ribosome-bound form. A variety of purification techniques, including affinity chromatography and ultracentrifugation, will be used during the purification of macromolecular complexes. Purified assemblies will be then investigated functionally. Students will then characterise their samples structurally through transmission electron cryo-microscopy (cryo-EM), including sample preparation, microscopy, data evaluation and the calculation of densities. Finally, students will learn how to build and refine molecular models into parts of the calculated cryo-EM density. The participants will be working on a closed project related to current research within the laboratory and throughout the course the practical work will be accompanied by brief theoretical introductions. The principal aim of the course is to strengthen the skills required to independently conduct meaningful biophysical and biochemical experiments and to provide an early introduction into the structural characterisation of cellular macromolecular assemblies.
Resources
Lecture Notes
A script will be distributed at the beginning of the course that will cover the experiments to be performed, provide references to the relevant literature and suggest points for further consideration for interested students.
Literature
Literature A basic overview is provided within the references below. Further reading and citations shall be detailed in the course script. - A. Fersht, Structure and mechanism in protein science, Freeman, 1999 (Chapters 1 and 6). - M. van Heel et al., Single-particle electron cryo microscopy: towards atomic resolution, Quart. Rev. Biophys. (33), 307-369 (2000).
Learning Materials (Links)
- Moodle course
- Moodle-Kurs / Moodle course
General Information
- Language
- English
- Levels
- BSC
- Frequency
- Yearly recurring
Examination
- Type
- graded semester performance
Course Components
| Type | Title | Time & Place | Hours |
|---|---|---|---|
| practical/laboratory course |
Cryo-Electron Microscopic Studies of Ribosomal Complexes with Biomedically Important Viral Proteins
Permission from lecturers required for all students.
Block course in the 2nd quarter of the spring semester
|
|
100 h semesterly |
Offered In
-
-
-
Block Courses (Registration for Block courses is mandatory. Please register under . Registration period: 21.12.2023 to 10.01.2024. Please note the ETH admission criteria for the admission of ETH students to ETH block courses on the block course registration website under "allocation".)
-
Block Courses in 2nd Quarter of the Semester (From 14.03.2024 to 12.04.2024)
-
-
-
-
-
Block Courses (Registration for Block courses is mandatory. Please register under . Registration period: from 21.12.23 - 10.01.2024 Please note the ETH admission criteria for the admission of ETH students to ETH block courses on the block course registration website under "allocation".)
-
Block courses 2nd quarter of the semester (14.03.2024 to 12.04.2024)
-
-