CHIMICA BIOORGANICA
Academic Year 2016/2017 - 1° YearCredit Value: 8
Scientific field: CHIM/06 - Organic chemistry
Taught classes: 56 hours
Term / Semester: 2°
Learning Objectives
The course aims to provide the student with specialist knowledge on some of the topics commonly dealt with by Bio-Organic chemistry.
- The most recent developments in the field of the chemical synthesis of oligonucleotides and proteins.
- Biopharmacological properties of normal or modified antisense oligonucleotides, as well as the use of oligonucleotides in the field of RNA-interference.
- Mechanistic aspects in the working of some enzymes. Enzymatic biotechnologies.
- The role of substrate-receptor interactions in the field of pharmacologically active natural compounds.
Detailed Course Content
Preliminary notions for the study of bio-organic chemistry.
Bioisostery; proximity effects in organic chemistry; molecular adaptation.
Bio-organic chemistry of amino acids.
General properties; dissociation behavior; alkylation; acylation; asymmetric syntheses of amino acids.
Bioorganic chemistry of peptides.
Modern methods for the solid phase synthesis of oligopeptides;
Chemical synthesis of proteins;
Particular aspects of the "non-ribosomal" biological synthesis of oligopeptides;
The depsipeptides and the ionophores.
Bioorganic chemistry of the phosphoric group and oligonucleotides.
Hydrolytic pathways of the phosphoric group and pseudorotation;
Enzymatic catalysis for the hydrolysis of the phosphodiester bridge: the ribonucleases;
Synthesis in solution of oligonucleotides;
Solid-phase synthesis of oligonucleotides;
Liquid phase synthesis of oligonucleotides (HELP);
Advanced methods of chemical synthesis of oligo- and polynucleotides without the use of base protector groups;
Synthesis of oligonucleotides by chemical ligation.
Antisense nucleotides, and lipo-modified antisense nucleotides;
The new horizons of "RNA-interference".
Enzyme technologies
Immobilized enzymes: immobilization techniques on various organic and inorganic supports; enzymatic biotechnologies for preserving the native structure of enzymes;
The use of immobilized enzymes in the synthesis of organic molecules of pharmaceutical interest.
Enzymatic reactions in non-aqueous solvents.
Enzyme models.
From micelles to liposomes: mono- and multilamellar liposomes: techniques used for their preparation and characterization; their use in the pharmacological field.
Triggered-release liposomes and their pharmacological potential. Liposomes as chemical reactors; Molecular devices. Nanocapsules as Drug delivery systems.
Textbook Information
- H. Dugas, Bioorganic Chemistry (3rd ed.) Springer, New York
- M. Page and A. Williams, Organic & Bio-0rganic Mechanisms, Longman, Singapore.