626-0010-00L Nanomachines of the Cell (Part I): Principles
|Semester||Autumn Semester 2015|
|Lecturers||D. J. Müller|
|Periodicity||yearly recurring course|
|Language of instruction||English|
|Abstract||Molecular biotechnology students will combine basic knowledge in molecular cell biology, biochemistry, proteomics, biophysics, bioinformatics, bionanotechnology and engineering to learn how the nanomachines of the cell works and to use this knowledge to address future molecular biotechnological and bionanotechnological questions. Particularly it will be addressed how biomolecular units can be char|
|Objective||Gain of an interdisciplinary research and development competence, which qualifies for scientific work (master's or doctoral thesis) as well as for work in the research and development department of a biotechnological company. The module is of general use in nano- and biotechnological courses of study focusing modern biomolecular technologies.|
|Content||What are nanomachines of the cell? Understanding the cell as a complex factory. Are there engineering principles of the cell and if so what can we learn? Introducing new ways to understand and to apply engineering principles of cellular nanomachines in biotechnology and nanotechnology.|
Introduction into factors and mechanisms that determine protein folding and stability. Inter- and intramolecular interactions. Understanding the concept of an energy landscape to describe protein folding, stabilization, destabilization, and unfolding. Mechanisms of protein stabilization, destabilization and aggregation in health and disease. Are there methods and ways to prevent protein destabilization and aggregation? Mechanisms of protein destabilization in biomaterials science, bioengineering, and in biotechnological and pharmacological applications. Protein stability in biotechnology. Biophysical methods that allow quantifying protein stability. Methods to prevent protein destabilization in biotechnological applications. Ways to adjust and manipulate the protein stability in biotechnology and medicine. Designing molecular compounds that stabilize specific proteins. Designing molecular compounds that lead to protein destabilization, misfolding and denaturation.
Biological and artificial membranes. Principles of membrane assembly, properties, stability and durability. Vesicles as containers for cargo. Engineering vesicles from native and synthetic components. Engineering ultrastable synthetic vesicles. Applying vesicles in biotechnology and medicine. Functionalizing vesicular membranes with proteins. Principles of membrane proteins. Structure and function relationship of membrane proteins. Importance of membrane proteins in pharmacology and biotechnology. Ways to structurally and functionally characterize membrane proteins. Bionanotechnological tools to handle and manipulate single membrane proteins. Membrane proteins as a toolbox to assemble nanoscopic functional vesicles. Designing multifunctional synthetic vesicles: Vesicles for drug delivery, vesicles for active transport, vesicles converting energy, vesicles switching their affinity, function, stability, and other properties.
Energy currencies of the cell. Energy conversion. Storable and transient forms of energy. Nature created a variety of light-driven ion pumps. How can we use this pumps, how can we modify them to our purpose? Employing light-driven ion pumps in biotechnology. Employing light-driven proton pumps adsorbing different wavelengths to boost the membrane gradient. How to create a synthetic membrane that allows no diffusion of ions. Transforming a proton into a chloride pump. Tuning the adsorption spectra of a light-driven ion pump. Engineering proton pumps as safety standards for credit cards and ID cards. Engineering proton pumps for holographic devices. Native and artificial light-activated ion channels. Engineering light-activated channels for their use in neuroscience: Optogenetics. ATP synthases convert transient into storable energies. Experimental approaches to explore the nanoscopic rotary machinery of single ATP synthases. Are there ways to engineer and to exchange the building blocks of the ATP synthase? Ways to change to gear of ATP synthases and to 'tune' its fuel consumption. Engineering an artificial vesicular system to convert light into ion gradients to synthesize ATP. Engineering ATP synthases as nanopropellers to move vesicles. Engineering a light-frequency tuned proton pumps to control the speed of nanopropelled vesicles. Engineering light-driven ion pumps to power the synthetic ATP propellers and to steer vesicles. Engineering and employing ATP synthases as molecular mixing devices.
Principles of signal transduction. The family of G-protein coupled receptors (GPCRs). Structure and function of GPCRs. Engineering (and other) possibilities to manipulate the functional state of GPCRs.
|Lecture notes||Hand out will be given to students at lecture.|
|Literature||Alberts et al: Molecular Biology of the cell|
Biochemistry (5th edition), Jeremy M. Berg, John L. Tymoczko, Lubert Stryer; ISBN 0-7167-4684-0, Freeman
Principles of Biochemistry, Nelson & Cox; ISBN: 1-57259-153-6, Worth Publishers, New York
Cell Biology, Pollard & Earnshaw; ISBN:0-7216-3997-6, Saunder, Pennsylvania
Intermolecular & Surface Forces, Israelachvili; ISBN: 0-12-375181-0, Academic Press, London
Proteins: Biochemistry and Biotechnolgy, Walsh; ISBN: 0-471-899070, Wiley & Sons, New York
Textbook of Biochemistry with Clinical Correlations, Devlin; ISBN: 0-471-411361, Wiley & Sons, New York
Molecular Virology, Modrow et al.; ISBN: 3-8274-1086-X, Spektrum Verlag, Heidelberg
|Prerequisites / Notice||The module is composed of 3 SWS (3 hours/week): 2-hour lecture, 1-hour seminar. For the seminar, students prepare oral presentations on specific in-depth subjects with/under the guidance of the teacher.|