Credits
6
Types
Compulsory
Requirements
This subject has not requirements
, but it has got previous capacities
Department
UB
The structural principles of biopolymers: proteins and DNA
Prediction and analysis of three-dimensional structures of biomolecules and their complexes
Molecular simulations of proteins and DNA.
Teachers
Person in charge
- Josep Lluis Gelpi Buchaca ( gelpi@ub.edu )
Weekly hours
Theory
2
Problems
0
Laboratory
2
Guided learning
0
Autonomous learning
6
Competences
Knowledge
Skills
Objectives
-
1. Recognition of the structural patterns of biomolecules and relationship with their biological function. The student must demonstrate understanding of the physicochemical descriptors of structure: terms of potential energy, solubility, acidity, hydrophobicity
Related competences: K1, K2, K5, -
2. Correlate three-dimensional structure of biomolecules with their biological function
Demonstrate understanding of:
- Relationship between sequence, structure, and function: global and local flexibility and similarity of the sequence, three-dimensional preservation of active centres, conservation of interactions with ligands and other proteins.
- Bases and applications of the homology concept. Identify the conserved residues in structure and describe its possible structural function.
Related competences: K1, K5, K7, S7, -
3. Manage the software that allows processing data representing structures and sequences of biomolecules.
Related competences: K2, S7, S10,
Contents
-
Part 0. INTRODUCTION
Introduction to the course.Aims, position of structural bioinformatics within bioinformatics, main objectives. Application examples -
Part 1. STRUCTURE AND MODELLING
Fundamentals of macromolecular structures. Conformational space. Experimental structure determination. Data sources and formats. Databases and Molecular visualization.
Structural data quality, common issues and fixes.Structure comparison, Sequence/structural alignment, structural families, the concept of homology. Structure prediction (1D, Threading, Comparative, Ab initio, Alphafold). Complex prediction (Docking) -
Part 2. CONFORMATIONAL SPACE AND SIMULATION
Energy evaluation. Molecular force fields. System setup for simulation. Optimization of the simulation process and HPC. Strategies for improved comformation sampling. Simulation analysis. Quality control. Flexibility analysis. Strategies for entropy and free enegy evaluation. Advanced analysis. nmetwork analysis and AI-based methods -
Part 3. STRUCTURES IN SYSTEM BIOLOGY
Protein domains. Interactions between chains and between domains. Predicting physical interactions based on domains. Transitive and permanent complexes. Other predictions of relationships between genes and proteins. Communication systems and signalling networks (phosphorylation). Study of interaction networks: Interactome. Large macromolecular complexes.
Activities
Activity Evaluation act
Theoretical sessions
Content presentation sessions. Slide presentations and guided demonstrations.- Theory: 1 - INTRODUCTION. Introduction to the course.Aims, position of structural bioinformatics within bioinformatics, main objectives. Examples 2 - STRUCTURE AND MODELLING. Fundamentals of maclomolecular structures. Conformational spaces. Experimental structure determination. Data sources and formats. Databases Molecular visualization. Structural data quality, common issues and fixes.Structure comparison, Sequence/structural alignment, structural families, the concept of homology. Structure prediction (1D, Threading, Comparative, Ab initio). Complex prediction (Docking) 3- CONFORMATIONAL SPACE. Simulations. Molecular force fields. System setup for simulation. Optimization of the simulation process and HPC. Strategis for improved comformation samplint. Simulation analysis. Quality control. Flexible systems and use of molecular dynamics to explore flexibility. Strategies for entropy and free enegy evaluation 4 - STRUCTURES IN SYSTEM BIOLOGY Partition of protein domains. Interactions between chains and between domains. Predicting physical interactions based on domains. Transitive and permanent complexes. Other predictions of relationships between genes and proteins. Communication systems and signalling networks (phosphorylation). Study of interaction networks: Interactome. Large macromolecular complexes.
Contents:
Theory
27h
Problems
0h
Laboratory
0h
Guided learning
0h
Autonomous learning
20h
Guided structural analysis
Resolution of practical cases on bioinformatics analysis tools, usually available via the web, or easily installableResolution of practical cases on bioinformatics analysis tools, usually available via the web, or easily installableObjectives: 1 2 3
Contents:
Theory
0h
Problems
0h
Laboratory
14h
Guided learning
0h
Autonomous learning
30h
Intregrated Analysis project
Free-subject project that involves the use of structural analysis or prediction tools developed during the course, applied to the understanding of the structure-function relationship of a protein system.
Theory
0h
Problems
0h
Laboratory
2h
Guided learning
0h
Autonomous learning
20h
Teaching methodology
- The theoretical classes will be expository with the help of graphic materials (slides, videos, computer demonstrations).- The problem-solving session will detail the methodology for solving the selected problems. It will include expository and practical sessions.
- The guided structural analysis sessions will be held in "Hackathon" style working groups to solve the use of structural bioinformatics tools for the resolution of practical cases.
Evaluation methodology
For the evaluation of the subject, the grade of the partial exam (MTE) and final exam (FE) and the grade of the practical sessions and the analysis project (Proj) will be taken into account according to the following formula:Grade = MTE * 0.2 + FE * 0.6 + Proj * 0.2
A grade equal to or greater than 5 is required to pass.
The Practical Sessions and Project (Proj) qualification is conditional on a minimum in-person attendance of 60% in the practical/problem sessions.
Students who have failed with a grade equal to or greater than 3 may take the re-evaluation exam (RT). In this case, the grade of the subject will be 0.2 * Proj + RT * 0.8.
Bibliography
Basic
-
Structural Bioinformatics
- Gu, Jenny; Bourne, Philip E.,
Wiley Blackwell,
2009.
ISBN: 978-0-470-18105-8
-
Introduction to protein structure
- Branden, Carl; Tooze, John,
Garland,
cop. 1999.
ISBN: 978-0-8153-2305-1
https://discovery.upc.edu/discovery/fulldisplay?docid=alma991002888829706711&context=L&vid=34CSUC_UPC:VU1 -
Molecular modelling : principles and applications
- Leach, Andrew R,
Prentice Hall,
2001.
ISBN: 9780582382107
https://discovery.upc.edu/discovery/fulldisplay?docid=alma991002680539706711&context=L&vid=34CSUC_UPC:VU1 -
The Biophysical chemistry of nucleic acids & proteins
- Creighton, Thomas E,
Helvetian Press,
2010.
ISBN: 9780956478115
https://discovery.upc.edu/discovery/fulldisplay?docid=alma991005476510806711&context=L&vid=34CSUC_UPC:VU1
Previous capacities
Basic knowledge of macromolecule structure (Physical and organic chemistry, Biochemistry, Molecular Biology)Knowledge of Thermodynamics and kinetics and evaluation of energies in macromolecules (Physical and organic chemistry, Biophysics)
Knowledge of molecular visualization tools
Knowledge of programming (python)