5 ECTS credits
125 h study time

Offer 1 with catalog number 4012689ENR for all students in the 2nd semester at a (E) Master - advanced level.

Semester
2nd semester
Enrollment based on exam contract
Impossible
Grading method
Grading (scale from 0 to 20)
Can retake in second session
Yes
Enrollment Requirements
Students must have followed ‘Biochemistry’, before they can enroll for ‘Regulation of cellullar processes’. Enrolling in ‘Regulation of cellullar processes’ means that you simultaneously follow 'Protein chemistry: function and structure' or have successfully passed ‘Protein chemistry: function and structure’.
Taught in
English
Faculty
Faculty of Sciences and Bioengineering Sciences
Department
Bio-Engineering Sciences
Educational team
Eva Hadadi (course titular)
Activities and contact hours
26 contact hours Lecture
26 contact hours Seminar, Exercises or Practicals
Course Content

Part 1:
Protein maturation and trafficking are essential processes that ultimately determine life at cellular level. Good functioning of these processes is a prerequisite for cells and organisms to survive, to adapt to ever-changing conditions in a flexible way and to defend themselves against attacks from the outer world.
In order to be able to understand life, it is a prerequisite to investigate the properties of the cellular environment into which enzymes and other proteins operate. Therefore, this course deals first with the cytoskeleton and the properties of the different elements belonging to this intricate structural network are discussed.
In the next chapter, emphasis is put on the association of proteins to form heterologous protein-protein aggregates. Such interactions are essential not only for the regulation of metabolic pathways (which relies on the formation of metabolons and channeling of metabolites) but for virtually every process taking place in a living cell/organism (e.g. in transcription and translation, signal transduction, in the immune system, during apoptosis, etc..).
The next chapter deals with protein trafficking. It is indeed essential for a cell that newly synthesized proteins are directed towards their correct final destination. Transport of proteins following the general export route via the endoplasmic reticulum and the Golgi apparatus is discussed. In close connection to this issue we look into the different types of protein glycosylation. These co-/post-translational modifications take place when newly synthesized proteins are transported through the ER and the Golgi complex. Next we discuss the import of newly synthesized proteins into eukaryotic subcellular organelles such as mitochondria, chloroplasts, peroxisomes, the nucleus and lysosomes.
Another chapter deals with folding of proteins in the cell. An overview is given of PDIs and PPIases, and of different chaperones and chaperonins that are essential molecules for the in vivo folding of proteins towards their correct three-dimensional structure. Recent structural information on these molecules and on their action is given.
Finally a last chapter describes post-translational modifications (glycosylation, ubiquitination, phosphorylation, nitrosylation, methylation, N-acetylation and lipidation) and their functional importance.  As an example the protein degradation process will be highlighted in details: We discuss on the structure and the action of the proteasome, which is an essential machinery involved in eukaryotic protein degradation. Attention is paid to the role of ubiquitin in this and in other cellular processes.

Part 2:
An important cellular process is the communication of the cells with the ‘outside world’ by which they can adapt to changing circumstances. With this respect plasma membrane receptors are key players. They are proteins that have a double function; recognition of neurotransmitters or hormones (denoted as chemical mediators) as well as translation of their binding into a cellular effect. This part comprises the following chapters:

  1. Chemical mediators and their receptors : definitions
  2. Classification of receptors (on basis of structure/function)
    In these two chapters of this part these endogenous chemical mediators are divided according to their mode of transmission (hormones, neurotransmittors) and according to their hydrophobicity (hydrophobic hormones which pass the cell membrane/ hydrophilic/large signalling molecules whose receptors are at the outside of the plasma membrane). These latter receptors are divided in the ways they trigger the cell response (activation of G proteins, endogenous phosphorylation, opening of ion channels).
  3. Ligand-gated ion channels
    This chapter deals with ligand mediated ion channels. With two typical examples the action mechanism of these receptor is explained. It concerns nicotinic acetylcholine receptor that operate the opening of sodium channels involved in the contraction of skeletal muscles and the glutamate and GABA mediated ion channels that are involved in rapid signal transduction in neurons.
  4. G-protein coupled receptors
    This chapter deals with G-protein coupled receptors. They represent a large family of plasma membrane receptors that are involved in a very broad range of (patho)-physiological processes. It is therefore not surprising that about 50 % of all commercial drugs act via modulation of these receptors. In this chapter their general mechanism of signal transduction is explained as well as their classification on basis of their structure/amino acid sequence.
  5. Growth factor receptors
    The next category of receptors are the growth factor or tyrosin kinase receptors. The binding of their ligands i.e. growth factors activates their intrinsic property of endogenous phosphorylation. As their name indicates, the binding of these ligands are involved in the regulation of cell growth and division.
  6. Steroïd receptors
    The last category of receptors are located intracellularly. They mainly recognize steroid hormones, which are apolar mediators that are able to cross the plasma membrane barrier.
  7. Methodology :  Analysing proteins & protein-protein interactions - classical and high throughput assays
    We will discuss assays including co-immunoprecipitation, pull-down assays, western blotting, mass spectrometry or sequencing based approaches.
  8. Methodology : Analysing proteins & protein-protein interactions - imaging techniques (in vivo and in vitro approaches)
  9. Methodology :  Analysing proteins & protein-protein interactions - novel technologies
  10. Role of proteins in diseases:

We will discuss about (1) misfolding & aggregation related diseases, (2) the role of histone modifications & other post-translational modifications, and (3) enzyme deficiencies. Pharmacological classification of receptors will be shortly covered.

Practical
During the practical we will perform measurements to detect post-translational modifications and/or signal transduction using classical techniques including flow cytometry or western blot.
 

 

Course material
Digital course material (Required) : Figuren en schema's die bij de cursus behoren (powerpoint presentatie) worden aan de studenten verstrekt.
Additional info

Participation to the practicals is mandatory.

Learning Outcomes

General competencies

To provide the student insight in the domain of Molecular Pharmacology. The acquired knowledge during this course is useful in a research-oriented career. It provides the bio-engineers the basic knowledge to perform pre-clinical research and to function within multi-disciplinary teams in the pharmaceutical industry.

This course aims to analyze various processes taking place within the living cell.
Students will:
-be able to describe the structural organization of the intracellular components of the cytoskeleton and its associating proteins.
-know and understand the properties of the intracellular environment.
-know and understand the advantages of heterologous protein-protein interactions and of metabolite channeling.
-be able to explain the problem of protein trafficking in the cell in all its aspects.
-know and understand the process of protein folding in the cell.
-be able to describe the process of protein degradation in the cell.
-know and understand the different functions of the protein ubiquitin and of ubiquitin-like molecules.
-be able to make an analysis of different technologies that are used in these domains of research.

 

Grading

The final grade is composed based on the following categories:
Written Exam determines 75% of the final mark.
PRAC Practical Assignment determines 25% of the final mark.

Within the Written Exam category, the following assignments need to be completed:

  • Written exam with a relative weight of 1 which comprises 75% of the final mark.

Within the PRAC Practical Assignment category, the following assignments need to be completed:

  • WPO with a relative weight of 1 which comprises 25% of the final mark.

Additional info regarding evaluation

Exam:
Written exam: 3hrs, the test contains multiple choice questions, 2 open questions on the general topic and 4 problem solving technical questions.

Evaluation:
Grade = ¾ written exam, ¼ practical
Attendance of the practical is obligatory! After the practicum the students need to submit a written report in which the following items are included: introduction, aim, used techniques, analysis and discussion of the results and conclusion(s). 
 

Allowed unsatisfactory mark
The supplementary Teaching and Examination Regulations of your faculty stipulate whether an allowed unsatisfactory mark for this programme unit is permitted.

Academic context

This offer is part of the following study plans:
Master of Bioengineering Sciences: Cell and Gene Biotechnology: Molecular Biotechnology (only offered in Dutch)