LPhD131 Heterologous gene expression

Details
Responsible DepartmentDepartment of Plant Biology and Biotechnology   90 %
Department of Food Science   5 %
Department of Basic Animal and Veterinary Sciences   5 %
Department of Basic Science and Environment   0 %

Research SchoolBiotechnology (FOBI)
 
Course DatesBlock 3, 2012, beginning February 6th
 
Course Abstract"Heterologous expression" is a vital course for students who intend to work with the production and/or use of recombinant protein in the biotechnology industry or as a tool in their basic research.
 
Course Home Pagehttp://www.kursusinfo.life.ku.dk/Kurser/240020/pre...
 
Course RegistrationSend email to Anja T. Fuglsang atf@life.ku.dk
 
Deadline for RegistrationDecember 1, 2011
 
Credits15 (ECTS)
 
Level of CoursePhD course
 
Language of InstructionEnglish
 
Restrictions40
 
Course Content
Course Content
The course will contain a theoretical part where most aspects of peptide and protein production in biological organisms will be discussed (see below). You will acquire knowledge on the variety of possible host organisms found in the different kingdoms. We will discuss the possibilities of designing and finding new suitable expression hosts.

Topics that will be covered in the theoretical part of the course:
The intelligent choice of a host organism / Cloning strategies envisioned by an "in silico" multistep cloning / Promoter strength and induction / Copy number and silencing problems in heterologous hosts / Expression vectors / mRNA stability and introns / Choice of, and placement of purification tags / Stability of the product / Secretion of proteins and signal trapping / Post-translational modifications in different host organisms / Inclusion bodies and folding of proteins / Expression of membrane proteins compared to soluble proteins / Heterologous expression for production of antibodies / Expression of toxic proteins / Transient expression / Optimisation of expression level / Fermentation and large scale production.

In the practical part of the course we will work with a range of different expression organisms. These include Escherichia coli, Saccharomyces cerevisiae, Pichia pastoris, Xenopus oocytes and higher plants. We will transform them and determine the amount of produced protein, we will also discuss ways to optimize the expression level and finally prove that the expressed protein exhibit the desired function.
In the practical part we will also cover a broad aspect of typical problems related to the production of recombinant protein.

Topics from the practical part of the course:
Expression and assembly of a multi subunit protein complex / The effect of alcohol and temperature on expression level / Expression of a secreted protein / Sub-cellular fractionation / Detection of post-translated modifications / The use of protein homologs from thermophilic bacteria /Yeast two-hybrid system/ Split-Ubiquitin system / Electrophysiological measurement on ion-channels/ Virus induced expression
 
Teaching and learning Methods
Teaching and learning Methods The course contains both a theoretical part and a practical part. In the theoretical part there will be lectures as well as student presentations based on cases and journals. A practivcal laboratory part is running several days during most weeks. There is a close connection between the topics covered in the theoretical cases and the practical work. The course will be divided into smaller parts build upon the different expression organisms.
 
Learning Outcome
Learning Outcome
The production of technical enzymes as well as of peptide- and protein-based pharmaceuticals are in large scale being performed in specially designed host organisms. The aim of the course is to educate the students in processes associated with heterologous expression. The students will upon completion of this course be able to design and perform a strategy for the expression of a given gene. This includes considerations about amount, quality and downstream applications of the product.

After completing the course the student should be able to:
Knowledge:
-Describe the main features of E.coli, Bacillus, S.cereviiae, P.pastoris, mammalian cell lines, Xenopus oocytes, Aspergillus and plants as expression hosts
-Describe the following parameters for the above mentioned expression systems: Expression levels, Type of post-translationel modifications, Mechanisms for secretion of the product, Stability of the product, Stability of the transformed expression host, Methods commonly used for transformation, Strategies for optimization of the expression level and quality of the product.

Skills:
-Use the knowledge to design an appropriate strategy for the expression of the correct amount and quality of a given protein/peptide.
-Design a strategy for creating an optimal genetically modified expression host in relation to reduction of proteases, improvement of secondary modifications and efficient compartmentation of the desired product.

Competences:
-Transfer theory and principles regarding the usefulness of different organisms as expression hosts to different work situations.
-Make ethic considerations about the use of GM organisms for production of peptides and about the disease risks connected to a certain expression host.

 
Course Literature
Course Literature
The students will receive a collection of scientific papers together with the manuals for the laboratory part of the course.
 
Course Coordinator
Anja Thoe Fuglsang, atf@life.ku.dk, Department of Plant Biology and Biotechnology/Section for Transport Biology, Phone: 353-32586
 
Other Lecturers
BLP, Bent Larsen Petersen DK, Dan Klærke MA, Merete Albrechtsen NA, Nils Arnborg RL, Rosa Lopez TP, Thomas Pomorski PEJ, Poul Erik Jensen KEA, Keld Ejdrup Andersen
 
Type of Evaluation
Evaluation of reports and participation
 
Work Load
lectures24
practicals140
theoretical exercises28
preparation104
project work116

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