Team:Virtus-Parva Mexico/Project
From 2014.igem.org
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- | Having done this, we then prepped our protein by resuspending it in a mix of Tris/acetate and EDTA in order to be able to combine it with our DNA. Then we dispersed our magnetite in anhydric toluene and we added the resuspended protein and we added as well some glutaraldehyde as a coupling agent. We also made some batches without any glutaraldehyde, to compare the comparable strength of their bonds. | + | <font color="#ffffff">Having done this, we then prepped our protein by resuspending it in a mix of Tris/acetate and EDTA in order to be able to combine it with our DNA. Then we dispersed our magnetite in anhydric toluene and we added the resuspended protein and we added as well some glutaraldehyde as a coupling agent. We also made some batches without any glutaraldehyde, to compare the comparable strength of their bonds. |
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Revision as of 03:16, 18 October 2014
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What is it that we do?
The Bio-NEMS drill is the project that we, a group of nanotechnologists have Project Overview
Virtus-Parva is a team of Nanotechnology students who aim to create a better world through love,sympathy and endearment… and through the design and development of a novel technology based on micrometric “drills” that can penetrate diverse organisms.
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The Idea
The basis for these “drills” will be NEMS, nano electro-mechanical systems, technology. NEMS NEMS are nanometric electromechanical systems. In this case we take as basis the structure of a resonator which are engineered to make a conversión between energy, such as electric, magnetic, or vibrational into mechanical response.
DNA Coiling
Naturally, and as part of the process of transcription DNA is wrapped around protein molecules called histones. The combined loop of DNA and protein is called nucleosome, and this nucleosome is going to be packed into a thread. Our objective was to insert magnetite into this system, in order to convert it into a NEMS and be able to control DNA’s movement using an external stimuli.
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The MakingThe most important part of our project was the time that we dedicated to seeing results in our lab. Admittedly, it was tough, for we had to do everything in our own time and we had only occasional help from our instructors, for the most part we did everything on our own. Despite all of the size of the challenge, our team rose up to the occasion and in the end all those hours we dedicated in the lab were worth it. Here you can see a short description of what all the things we did in our lab, for a more detailed description check our notebook section. Inorganic Section
The first part of the synthesis of our magnetite was trying out different methods and characterizing them, to note which method had given us the smallest size nanoparticles. Our first method was synthesis by coprecipitation, of which we prepared nine samples with different concentrations of iron(II) chloride and ammonium hydroxide; from this method we consistently obtained nanoparticles rounding 0.9 to 1nm. Our following method was very similar, but included water in the synthesis: the size of our particles would vary greatly, from 3.89 micrometers to 171 nanometers in size.
Biological Section
Having done this, we then prepped our protein by resuspending it in a mix of Tris/acetate and EDTA in order to be able to combine it with our DNA. Then we dispersed our magnetite in anhydric toluene and we added the resuspended protein and we added as well some glutaraldehyde as a coupling agent. We also made some batches without any glutaraldehyde, to compare the comparable strength of their bonds.
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