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| [[Image:bch.jpg|thumb|100px|right|that's me]] | | For information on me, see [http://thebryanhernandezgame.wordpress.com/ The Bryan Hernandez Game]. |
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| == Bio == | | == Bio == |
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| *I am currently a UROP in the [[Endy Lab]] working with [[Jason Kelly]]. | | *I am currently an undergraduate researcher in the [[Endy Lab]] at MIT. I am currently building and characterizing orthogonal riboregulators. Learn more about riboregulators and the work I have done [http://parts2.mit.edu/wiki/index.php/Berkeley2006-RiboregulatorsMain here] |
| *MIT Class of 2009; Majoring in Mathematics and Biological Engineering. | | *MIT Class of 2009; Majoring in [http://math.mit.edu/| Mathematics] and [http://web.mit.edu/be/index.htm| Biological Engineering]. |
| [[Image:flag California.jpg|thumb|100px|center|home]]
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| == Projects == | | == Projects == |
| ===[[Sortostat]]===
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| *We are currently using strain [[Genotypes#MC4100|MC4100]] E.Coli capable of expressing CFP and YFP (Cyan Fluorescent Protein and Yellow Fluorescent Protein, contained on plasmid [http://parts.mit.edu/r/parts/partsdb/view.cgi?part_id=4659 pSB1A2] ) as these are easily distinguished between visually thereby aiding in our descriminitive assortment without relying on chemical selection. In this way, it is less likely for cells to avoid being sorted by a genetic mutation as one might expect using an antibiotic.
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| *[http://www.midgard.liu.se/~b00perst/chemostat.pdf Chemostat Theory]
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| *[[Sortostat/Experiments]]
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| *[[Sortostat/Growth Tests]]
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| '''Project Goals''' | | ===Construction and Characterization of Riboregulators=== |
| | A Riboregulator is a post-transcriptional regulator used in bacteria. Its mechanism for regulation involves the occlusion of the Ribosome via a hairpin on the mRNA transcript in the 'off' state thereby preventing (or 'locking') translation of the ORF. The 'on' state is recovered by introducing a complementary sequence (or 'key') that disrupts the hairpin on the mRNA transcript allowing the Ribosome to bind and initiate translation. To learn more, go [http://parts2.mit.edu/wiki/index.php/Berkeley2006-RiboregulatorsMain here]. |
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| *[[Bryan Hernandez/UROP Proposal|UROP Proposal]] | | *[[Bryan Hernandez/UROP Proposal|UROP Proposal]] |
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| *[[Sortostat]] | | ===[http://parts2.mit.edu/wiki/index.php/University_of_California_Berkeley_2006 Addressable Conjugation in Bacterial Networks]=== |
| | *Our project was to create an addressable cell-to-cell communication mechanism in e. coli.<br> |
| | *[[IGEM:UC Berkeley/2006 | iGEM UC Berkeley]] |
| | *[[IGEM:UC Berkeley/2006/bryans notebook|notebook]]<br> |
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| #Debug a microfluidic chemostat ([[Sortostat]]) to improve the time-varying specific selection of cell populations.
| | ===[[Sortostat]]=== |
| #*Currently troubleshooting problems: i) Cell Death after 3-4 days (presumably due to oxygen depletion,) and ii) Inaccurate cell counts due to poor image processing.
| | The Sortostat is a microfluidic chemostat integrated with a cell sorter. My project consists of demonstrating the sortostat's chemostat functionality, a technique rarely seen in microfluidics. |
| #Evaluate the response of populations of E.Coli cells containing engineered genetic circuits (http://parts.mit.edu) to particular selective pressures using the Sortostat.
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| | '''Immediate Goals''' |
| | *Debug all engineering-related problems with sortostat. |
| | *Demonstrate Sortostat's ability to attain chemostasis in a population of E. Coli. |
| | *Demonstrate Sortostat's ability to sort two phenotypically different populations of E. Coli. In this case, I will be using a mixture of E. Coli expressing CFP and YFP. |
| | *Demostrate Sortostat's ability to select for an arbitrary population of cells that are phenotypically different from others and maintain this population at a steady state. |
| | *[[Bryan Hernandez/UROP Proposal|UROP Proposal]] |
| | *[http://www.midgard.liu.se/~b00perst/chemostat.pdf Chemostat Theory] |
| | *[[Sortostat/Experiments]] |
| | *[[Sortostat/Growth Tests]] |
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| ===[[Endy:Evolutionary stability project|Evolutionary stability project]]===
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| It is known that mutations are more likely to occur with higher cell division rates. Everytime a cell divides it runs the risk of making a mistake in the replication process and creating a mutant cell. Evolution is largely in debt to this phenomonon; without mutants an organism's genome would be nearly static. However, beneficial this might be to the survival of a species, it poses a problem for our genetically engineered cells. If a cell divides and mutates in the process it could "break" our engineered genetic device. The cell will likely go on living, however, it will cease to perform its intended function. This is an unfortunate reality of biological engineering, and, as such, we must learn the characteristics of our devices and their liklihoods of "breaking."
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| In order to obtain a quantitative measure of how "fast" our devices break we will first need a controlled environment. By using a chemostat we can control the rate at which cells divide enabling us to calculate the number of cell divisions that have occured over some time. Note that number of divisions is but one variable that can be used to characterize the longevity of a device. One might imagine testing other variables such as temperature or cell cycle position for example, both of which likely have an effect on the "breaking rate."
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| Detecting when a cell's device has broken can be a challenge in it of itself; however, this challenge becomes much easier with the correct choice of device. We are using a device such that it's success is fatal to the cell under certain conditions, however, when the device breaks the cell lives and will grow. This is known as a counter-selectable marker and allows us to ultimately find out the rate at which our device breaks.
| | [[Bryan Hernandez/20.109|20.109]]<br> |
| | [[IGEM:UC Berkeley/2006/bryans -80 stocks|-80 stocks]]<br> |
| | [[media:oligos.xls|oligos]] |
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| Once a mutation rate is established, we can talk quantitatively about device longevity under prespecified conditions. We also, and more importantly, have a valid control in which to compare methods of prolonging a devices life which go beyond that of the counter-selectable marker. Our aim is to show that by remapping the cell's codon space we will be increasing the device's life.
| | contact me at bryanh (AT) mit |
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