SMPS20001U Biopharmaceuticals: Design and Modification of Biomacromolecules
MSc Programme in Medicinal Chemistry - compulsory
MSc Programme in Pharmacy (Danish programme cand.pharm) - elective
MSc Programme in Pharmaceutical Sciences (Danish programme cand.scient.pharm) - restricted elective
MSc Programme in Pharmaceutical Sciences (English programme) - restricted elective
Besides an introduction to the concepts and methods that are relevant for investigating and understanding the physicochemical and pharmacological properties of macromolecules, the course focuses on the design, discovery, and applicability of biopharmaceutical drugs, primarily those based on peptides or proteins.
Furthermore, this course will form the basis for studies on optimization of pharmaceutical properties of peptides, proteins, and nucleic acids in relation to preclinial and clinical drug development. Finally, drug leads derived from these classes of macromolecules (e.g., peptidomimetics) will be discussed.
These subjects will be introduced via lectures (based on comprehensive reviews and primary research articles), while the class sessions will comprise student presentations and discussion of selected scientific articles in order to facilitate an in-depth understanding of both theoretical and practical aspects of biopharmaceutical drug research. In addition, some class sessions will comprise theoretical execises on the basic elements of the course (e.g. peptide synthesis and protein modification). Also, the course comprises practical exercises in peptide synthesis and biochemical assay performance in the laboratory. These exercises illustrate basic solid-phase peptide synthesis (SPPS) methodology and biochemical evaluation of enzyme activity. For each excercise a laboratory notebook should be kept in order to facilitate writing a mandatory group report, which also includes interpretation and discussion of the achieved results (Yield, LC-MS analysis, and Michaels-Menten parameters).
The most relevant compound classes and their
applications are briefly outlined below:
- Peptide- and protein-based drugs, inculding modified peptide and proteins (primary content of the course).
- Introduction to antibodies and therapeutic relevance.
- Introduction to oligonucleotides for gene therapy and antisense siRNA as putative biopharmaceutical drugs.
- Introduction to vaccines.
Methods and concepts:
- Importance of structure for pharmacological activity and suitable drug properties: charge, solubility, stability and delivery.
- Primary sequence and folding into secondary and tertiary structures and methods for manipulating these.
- Principles of solid-phase peptide synthesis (incl. combinatorial and parallel approaches) and optimization. Advanced peptide chemistry including selection of linkers, coupling reagents and protecting groups.
- Protein biosynthesis and modification: post-translational and chemical transformations.
- Genetic and protein engineering as a discovery and production tool for biological protein and peptide expression and modification.
- Practical manual solid-phase peptide synthesis and simple modification of proteins.
- Chemical protein synthesis and semisynthesis
The purpose of this course is to provide students with
theoretical knowledge on biopharmaceutical drug discovery as a
central part of contemporary and future interdisciplinary drug
discovery efforts in academia as well as in the biotech and
pharmaceutical industry. The focus will primarily be on
peptides and proteins as they currently constitute the most
important class of biopharmaceuticals.
An additional aim is to introduce students to methodologies related
to chemical synthesis, biological expression, and modification of
biopharmaceuticals with a focus on their applications in drug
discovery and development.
At the end of the course, students are expected to be able to:
Knowledge
- comprehend the steps involved in biopharmaceutical drug discovery
- understand aspects of chemical peptide synthesis relevant for biopharmaceutical drug discovery
- understand post-translational peptide/protein modifications
- understand methods used in chemical peptide and protein modification
- understand the concept of non-canonical amino acid mutagenesis
- appreciate of the potential of novel types of biopharmaceuticals (e.g., nucleic acids and analogs thereof) in sufficient detail to follow future scientific developments
Skills
- search and read relevant literature and use this knowledge in biopharmaceutical research projects.
- perform solid-phase peptide synthesis
- conduct and enzyme kinetic experiment
Competences
- read and discuss research examples concerning optimization of biologically active peptide drug leads with respect to pharmacological properties including bioavailability and in vitro cytotoxicity
- apply basic theory of peptide optimization and protein engineering/expression related to practical development of biopharmaceuticals
Selected book chapters:
Peptide Synthesis and Applications, K. J. Jensen, A. P. Tofteng, S. L. Pedersen (Eds), Springer Protocols, Humana Press, 2013.
Supplementary reviews and research papers covering the
following topics:
Examples of subclasses of potential drug
leads (peptides, peptidomimetics and proteins), known
biopharmaceuticals (e.g. peptide hormones, cytokines, antibodies,
nucleic acids and analogues thereof.
All teaching materials besides the textbook will be available
via the course homepage or as handout
material.
Class sessions: 12
Writing of individual study report (ca. 40 hours during last 3 weeks)
Practical exercises (20 hours in lab)
- Category
- Hours
- Lectures
- 21
- Class Instruction
- 8
- Preparation
- 88
- Theory exercises
- 4
- Laboratory
- 20
- Project work
- 40
- Exam
- 25
- Total
- 206
Throughout the duration of the course period, students will be given the opportunity to answer multiple choice questions online, to which the answers are provided subsequently. This will provide them with an idea of their level of understanding of the taught curriculum.
Open for credit transfer students and other external students. Apply here:
Credit transfer students:
Credit transfer student at SUND – University of Copenhagen (ku.dk)
Other external students:
http://healthsciences.ku.dk/education/student-mobility/guest-students/
Credit transfer and other external students are welcomed on the course if there are seats available and they have the academic qualifications.
- Credit
- 2,5 ECTS
- Type of assessment
- Requirement to attend classesWritten assignment
- Type of assessment details
- Course certificate: The students work in groups of 3-5 persons preparing a joint lab journal and report on the performed experiments including answering of the associated questions.
- Aid
- All aids allowed
The lab teachers may be approached for guidance in answering the associated questions.
- Marking scale
- passed/not passed
- Censorship form
- No external censorship
- Re-exam
No re-exam available.
Criteria for exam assesment
To obtain a course certificatethe student must be able to:
Knowledge:
- show that the basic concepts have been understood through answering the associated questions.
- show that the basic concepts have been understood.
- a theoretical background to understand synthesis descriptions of simple chemical reactions involving peptides relevant as biopharmaceuticals.
Skills:
- carry out the laboratory work to satisfaction.
- perform experiments with acceptable results and described in a scientific way, so that the synthesis and analysis excercises may be repeated.
- performing simple syntheses and analysis of peptides.
Competences:
- write a report in a scientific language about how the experimental work was performed.
- Credit
- 5 ECTS
- Type of assessment
- Written assignment
- Type of assessment details
- Individual written assignment (essay) in the format of a scientific minireview (size: min 15.000 and max. 20.000 characters including spaces; supporting figures allowed) based on literature studies on a subject agreed upon with one of the teachers and approved with the course directors. The essay must relate to a substantial content of chemistry as well as a biology/biopharmaceutical aspect. The student will have 3 weeks to prepare this.
- Aid
- All aids allowed
- Marking scale
- 7-point grading scale
- Censorship form
- No external censorship
Criteria for exam assesment
To achieve the grade 12 the student must be able to:
Knowledge
- comprehend the steps involved in biopharmaceutical drug discovery
- understand aspects of chemical peptide synthesis relevant for biopharmaceutical drug discovery
- understand post-translational peptide/protein modifications
- understand methods used in chemical protein modification
- understand the concept of unnatural mutagenesis
- appreciate the potential of novel types of biopharmaceuticals based on nucleic acids (and analogs thereof) in sufficient detail to follow future scientific developments in this field
Skills
- devise chemical synthesis of relevant peptides and modification of protein drugs
- search and read relevant literature and use this knowledge in biopharmaceutical research projects.
- discuss and illustrate how a specific type of biopharmaceuticals may be discovered via synthesis/expression of leads that undergo optimization using appropriate methodologies.
Competences
- read and discuss research examples concerning optimization of biologically active peptide drug leads with respect to pharmacological properties including bioavailability and in vitro cytotoxicity
- apply basic theory of peptide optimization and protein engineering/expression related to practical development of biopharmaceuticals
Course information
- Language
- English
- Course code
- SMPS20001U
- Credit
- See exam description
- Level
- Full Degree Master
- Duration
- 1 block
- Placement
- Block 1
- Schedule
- C
- Course capacity
- 45 students
Study board
- Study Board of Pharmaceutical Sciences
Contracting departments
- Department of Drug Design and Pharmacology
- Department of Chemistry
Contracting faculty
- Faculty of Health and Medical Sciences
Course Coordinators
- Kristian Strømgaard (kristian.stromgaard@sund.ku.dk)
- Christian Adam Olsen (cao@sund.ku.dk)
Lecturers
Kristian Strømgaard
Christian A. Olsen
Knud J. Jensen