Besides the conference agenda we have organized on 5th and 6th of
September workshops and tutorials, respectively, on hot topics
including:
Proteomics Bioinformatics: From raw MS-data to knowledge
Advanced RNA-Seq and ChIP-Seq data analysis
Metagenomics
Phylogenomics
Data Integrity
The early registration deadline is on 15th Sep 2017.
For any additional information please do not hesitate to contact me or
Ms. Choulaki gh@imbb.forth.gr
Time:
12:00
Location:
FORTH Seminar Room 1
Description:
Dr Kathryn Melzak
Institute for Functional Interface (IFG), KIT, Karlsruhe, Germany
Red blood cell storage and the effects of diethylhexylphtalate (DEHP) plasticizer
Abstract
Bags used to store blood for transfusions contain the plasticiser diethylhexylphthalate (DEHP). The DEHP is regarded as a potential toxin, and is on EU lists of chemicals to be restricted. One challenge with finding an alternate plasticiser is that the DEHP has a beneficial effect, improving the quality of the stored RBCs; replacements will therefore have to have similar effects in order to maintain the standards of the blood supply. The mechanism by which DEHP exerts its effects is unknown. The work presented here is about the interaction of the DEHP with the RBC membrane, with some comments on how this can affect the RBC shape during storage.
Date: 14/9/2017
Time:12:00 (coffee & cookies will be served at 00:00)
Affiliation: Lower Saxony Centre for Biomedical Engineering Implant
Research and Development Department of Cardiothoracic, Transplantation &
Vascular Surgery,
Hannover Medical School
Title: From the Heart to the Lung and Back: Engineering the Path
Cardiovascular and pulmonary diseases are the leading causes of
morbidity and mortality, being among the top 3 diseases in terms of
healthcare spending worldwide. Valve replacement or repair is the 2nd
most common major heart operation in the western world, whereas vascular
stenting represents one of the most commonly performed procedures for
treating occlusive coronary artery disease. Moreover, lung
transplantation still remains the only viable option for the treatment
of patients with end-stage lung diseases, such as chronic obstructive
pulmonary disease (COPD), with extracorporeal membrane oxygenation
(ECMO) representing the current clinical practice as a bridge to
transplantation.
Currently, synthetic biomaterials chemically cross-linked animal or
human donor tissues are most commonly used for cardiovascular tissue
repair or replacement. However, conventional approaches only deliver
inert or biocompatible material solutions that prevent cellular
migration after implantation and cannot regenerate or grow with the
patient. Surgeons prefer autologous tissue since it will retain
viability and regenerate. However, autologous tissue is limited or not
available at all. Tissue engineering offers an attractive alternative
for cardiovascular tissue reconstructions, aiming to develop
tailor-made, functional substitutes for implantation, with the purpose
of fostering remodelling and regeneration of diseased tissue.
In the case of ECMO, the use of oxygenator devices is limited to a few
weeks due to contact of the patientʼs blood with the artificial
components of the device, and the consequent thrombus formation and
deposition of blood components within the device. The improvement of the
haemocompatibility of current ECMO devices does not only have the
potential to prolong ECMO usage in anticipation of a suitable lung
transplant, but it can also provide a destination therapy, as an
alternative to lung transplantation. To this end, surface
endothelialization has been considered an effective approach to enhance
long-term haemocompatibility of blood-contacting devices, such as
circulatory assist devices and stents.
This seminar will present an overview of the work undertaken at Hannover
Medical School in the fields of valvular tissue engineering and
biohybrid devices, including artificial lung and stents.
Host: Anna Mitraki 4095
Time:
15:00 - 16:00
Location:
Main Amphitheater “G. Lianis”, FORTH’s bldg
Description:
IMBB SEMINAR
(The seminar is part of the Chemical Biology of Disease Conference)
Peter SEEBERGER
Professor
Max-Planck Institut for Colloids and Interfaces
Am Mühlenberg 1, 14476 Potsdam (Germany)
peter.seeberger@mpikg.mpg.de
Title: "Glycocconjugate Vaccines Against Bacterial Infections Based on Synthetic Glycans"
Friday, September 15th 2017 @ 15:00
Main Amphitheater “G. Lianis”, FORTH’s bldg
Host: Inga Siden-Kiamos
Time:
12:00 - 13:00
Location:
Chemistry Seminar Room
Description:
CHEMISTRY SEMINAR
SPEAKER: Dr. Rubén D. Costa, IMDEA Materials Institute Technogetafe, Erik Kandel 2, 28320 Getafe, Madrid E-mail:ruben.costa@imdea.org
TITLE: Novel Approaches in Thin-film Lighting Technologies
DATE: Monday, 18 September 2017
TIME: 12:00
ROOM: Chemistry Seminar Room
Time:
12:00 - 13:00
Location:
Main Amphitheater “G. Lianis”, FORTH’s bldg
Description:
IMBB SEMINAR
Christos GATSOGIANNIS
Max Planck Institute Molecular Physiology
Department of Structural Biochemistry
Title: "High-resolution structure analysis of pore-forming proteins by cryoEM"
Tuesday, September 19th 2017 @ 12:00
Main Amphitheater “G. Lianis”, FORTH’s bldg
Host: M. Kokkinidis
Time:
14:00 - 15:00
Location:
Chemistry Seminar Room
Description:
CHEMISTRY SEMINAR
SPEAKER: Michael Krom
Professor (Emeritus) School of Earth and Environment, Leeds University, UK and Department of Marine Biology, University of Haifa, Israel
TITLE: How atmospheric processes change the bioavailability of P in dust and how important that process is globally ?
DATE: Tuesday, 19 September 2017
TIME: 14:00
ROOM: Chemistry Seminar Room
Time:
14:00 - 15:00
Location:
Main Amphitheater “G. Lianis”, FORTH’s bldg
Description:
FORTH SEMINAR
Professor Jean-Pierre BOURGUIGNON
President of the European Research Council (ERC)
Title: "ERC: A European Success Story"
Wednesday, September 20th 2017 @ 14:00
Main Amphitheater “G. Lianis”, FORTH’s bldg
Host: N. Tavernarakis
Time:
12:00 - 14:00
Location:
Seminar Room 1 FORTH
Description:
In vivo gene delivery seminar
12.00 - 12.45 Scientific Seminar about the GONAD technique (Kosteas)
12.45 - 13.00 Presentation of the current status of Infrafrontier program and related restructuring the Animal Facility (Talianidis-Kosteas)
13.00 - 13.45 Discussions about the need cryopreservation protocols and new gene targeting approaches.
Time:
11:30 - 12:30
Location:
Αίθουσα Τηλεδιασκέψεων, Τμήμα Βιολογίας
Description:
Πρόσκληση παρουσίασης διδακτορικής διατριβής
Αριάδνη Πριγκηπάκη
Παραγωγή και χαρακτηρισμός βιοεμπνευσμένων υλικών σε βακτήρια
Abstract
We investigate collective motion and relaxation in model polymeric glass-forming liquids by molecular dynamics simulation to quantify the
nature of cooperative motion in these liquids and to understand the significance of cooperative particle exchange motion for understanding relaxation properties of glass-forming liquids generally. We find that
relaxation occurs as multi-stage process involving cooperative molecular motion. First, there is a ‘fast’ or b-relaxation process dominated by the inertial motion of the molecules, followed by a longer time
a-relaxation process involving large scale diffusive motion. Our molecular dynamics simulations indicate that as the collective motion of the b-relaxation regime becomes progressively suppressed upon approaching Tg, material relaxation requires larger scale collective motion involving molecular diffusion, explaining the emergence of the a-relaxation regime. In both relaxation regimes, relaxation occurs through a string-like collective particle exchange motion having a common string-like geometrical form and quantitative relationships are derived relating the length of the ‘stringlets’ found in the b-relaxation regime to the ‘strings’ characterizing collective motion at long times associated with the thermally activated diffusive motion. Based on this physical picture, we find that the a-relaxation time data for a wide range of simulated glass-forming liquids can be described by an extension of the Adam-Gibbs model in which the free energy of activation (including the entropy of activation neglected by AG) is proportional to the average length L of string-like particle exchange clusters. This same type of collective motion arises in the grain boundaries of polycrystalline materials, the interfaces of
nanoparticles, superheated crystals, and in biological materials such lipid membranes and proteins so that string-like collective motion is evidently a common feature of strongly-interacting condensed matter.