Biological chemistry ii
Bachelor's degree
In Maynard (USA)
Description
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Type
Bachelor's degree
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Location
Maynard (USA)
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Start date
Different dates available
The tools section includes information about various molecular graphics programs used to view three-dimensional structures in this course.
Facilities
Location
Start date
Start date
Reviews
Subjects
- Biological Chemistry
- Translation
Course programme
Lectures: 3 sessions / week, 1 hour / session
Recitations: 1 session / week, 1 hour / session
Voet, D., J. Voet. Biochemistry. New York: J. Wiley & Sons, 2003. ISBN: 9780471250906.
This course is divided into four subject area modules as described in the following table.
Size and Components of Cells and Implications with respect to Regulation
Size of cells and components and implications with respect to regulatory mechanisms.
Introduction to macromolecular machines.
Fatty Acid Synthases (FAS), Polyketide Synthases (PKS), and Non-ribosomal Polypeptide Synthases (NRPS)
Initiation, elongation, termination and implications in human health. A paradigm for thinking about PKS and NRPS.
Overview of the macromolecular machines with a common solution to the problems. Specific examples include erythromycin and enterobactin biosynthesis.
Cholesterol biosythesis and homeostasis: implications in disease.
Translation: Loading, Initiation, Elongation, and Termination - A Machine in Action; Introduction to G-proteins: Switches or Motors
An overview of translation: the players and the pacman view of the process.
Methods to study macromolecular interactions: reconstitution experiments, crystallography, cryoelectron microscopy, footprinting and crosslinking, presteady state kinetics.
Loading: tRNA synthases and their editing mechanisms.
G proteins: switches or motors, EF-Tu and EF-G as examples in the elongation process. Molecular mimicry at work.
The 50S ribosomal subunit: a view of peptide bond formation using RNA. Is chymotrypsin (a serine protease) a good model?
The use of translation equipment to generate proteins containing unnatural amino acids in vitro and in vivo.
Crypts and Chambers: Macromolecular Machines involved in Protein Folding and Degradation
Protein folding in vitro: Anfinsen's hypothesis.
Protein folding in vivo: Hsp70/Hsp40: DNAJ and DNAK as a paradigm.
Protein folding in vivo. Hsp6O Family (GroEL and GroES).
26S Proteosome and the role of Ubiquitin in degradation.
For one hour each week, Professor Ting will provide an in-depth view of technologies briefly outlined in class and used in the assigned journal papers. These classes will also be used to go over problem sets and to discuss lectures.
Assigned reading will include sections from your textbook to refresh your memory or to give you a good overview of a specific topic. It will also include a review article on each module to bring you up to date about recent advances in a specific area and an original paper that will highlight the use of a technique to solve a problem covered within the module. Additional background reading will be placed on reserve. Additional references will be given for those so inclined to read about one specific topic in more detail.
In class, we will demonstrate three-dimensional structures using Rasmol, a molecular visualization program. We will provide the pdb files along with Rasmol scripts for the structures discussed per module, so that students can view them at their leisure.
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Biological chemistry ii
