User:Emilienne

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20.109 Spring 2007

Last Name

Repak

First Name

Emilienne

Course/Minor

Course 20, minor in French, strong interest in neuroscience

Year of Graduation

2009

Telephone #

(267)566-1418

Email

emilie7 at mit dot edu

Have you taken

7.05/5.07 (Biochemistry) currently taking
7.06 (Cell Biology) no
7.02 (General Biology Lab) no
5.310 (General Chemistry Lab) no

Do you have any experience culturing cells (mammalian, yeast or microbial)?
No

Do you have any experience in molecular biology (electrophoresis, PCR, etc)?
No

Please briefly describe any previous laboratory experience

UROP in Fee Lab in McGovern Institute, BCS. February 06- present. I do brain surgery on songbirds (lesions, tracers, and electrophysiology), and I perform perfusions, histology, immunochemistry, and microscopy.

I am currently exploring the role of the auditory cortex in song development, following up on some interesting previous results from a post-doc in my lab. An interesting side effect of the lesioning surgeries I do (in which the auditory input is removed from the auditory cortex) is that our birds become fearless. This might make another exciting follow-up experiment!

Anything else you would like us to know?

Optional: As mentioned in lecture on 02.06.07, we would like you to consider how, as a biological engineer you might test the superstition "Spit on a bat before using it for the 1st time to make it lucky."

I would perform a double blind experiment in which both athletes testing bats and evaluators scoring performance of the bats do not know which bats have been spit upon. One could then statistically analyze the data from bats that had and had not been spit upon to see if bats with spit on them were any luckier. If, as I suspect, they are not, then I have proven that I do not need to go into molecular analysis of the spit to try to find the elements which contribute to the luck.

M13 Genome Engineering

Gene Functions and Re-engineering Ideas

GENE	FUNCTION	POTENTIAL MODIFICATION(S)
PI	Phage Secretion: C-terminals of P1 and P11 interact with N-terminal of P4 to form a complex through which mature phage are secreted.
PII	Replication: Initiates genome replication by nicking the double stranded phage DNA	Without P2, could the bacteria still make the phage gene products without replicating the phage DNA? If we remove P2 (and P5), could we use this virus to insert other genes into the bacteria? NOTE: Altering the second half of P2 will affect P10.
PIII	Rounded Tip of Filament: First protein to interact with the E. coli host pilus during infection and last point of contact as phages bud from bacteria. without P3, phage cannot fully escape host.	We might change P3 such that the phage was only capable of infecting a different host other than E. coli, if the need arose.
PIV	Phage Secretion: N-terminal of P4 interacts with C-terminals of P1 and P11 to form a complex (stable, barrel-shaped structure) through which mature phage are secreted.	Unless phages bottle-neck at the secretion complexes such that secretion becomes the limiting factor in phage production, it does not seem that modifying the proteins that form this complex will help expedite or even really alter our process
PV	Phage Packaging: sequesters + stranded phage DNA to be packaged into new phage particles	If we have a stronger promoter in front of this gene, phage packaging might occur faster, giving us more efficient production times. However, if too many + strands are taken away, this will hurt the DNA Replication process. Furthermore, no matter how many + strands are sequestered, we will still need enough coat protein to package these strands of DNA, so a strong promoter in front of this gene alone might prove useless.
PVI	Rounded Tip: Accessory to P3, buried	Is P6 needed? We could test this by increasing the production of P6 and/or by removing the gene for P6. What if we made P6 responsible for either the entrance or final escape from the host, such the P3 only carried on one of these tasks?
PVII	Blunt End: Companion to p9, buried	Is P7 needed? We could try increasing its expression and/or removing it if we wanted to test this.
PVIII	Phage Coat: Adjusts to size of genome it packages. ~2700 copies needed to make ~900 nm long coat	If we change the charge of P8, it will affect how the phage interacts with the surroundings. If we want to locate phages, we could also put markers into P8.
PIX	Blunt End	What is the role of the blunt end of the phage? Why not just have P3 on each side of the filament? We could try to test this in order to try to make the filament more versatile by making matching ends
PX	regulates number of double stranded genomes in the host. Without p10 no +strands can accumulate. Identical to C-portion of p2!	If we alter p10, we will affect p2. If we don't want phage DNA replication to occur, we can alter this gene.
PXI	Phage Secretion: C-terminals of P1 and P11 interact with N-terminal of P4 to form a complex through which mature phage are secreted.

M13 Design Constraints

Would you expect the phage to tolerate p8 modifications that: 1. make the protein neutral rather than negatively charged at the C-terminus?

It seems that the C-terminus may need to be charged in order to hold together the P8 proteins that make the phage coat. The charge may also be necessary for intermolecular interaction required to secrete the phage. It seems that a neutral protein will be less likely to have intermolecular interactions than a negatively charged protein, so I think that the phage would struggle to tolerate this modification. (I tried learning about the C-terminus of P8 from the abstract at the following site: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12217696&dopt=Abstract )

2. encode all the Leucines with the CTA codon instead of the CTG codon?

The codon sequence is not important as long as the appropriate amino acid is encoded, so the phage could tolerate this modification.

3. double the size of the protein?

It would be useful to know how the p8 knows how to regulate its production. Since the amount of p8 produced decreases when the genome size is decreased, this leads me to suspect that somehow the amount of p8 is being regulated such that the phage coat will always fit snugly over the phage’s DNA. Therefore, if the size of p8 is doubled, I suspect that only half the amount of protein will be used and the phage will tolerate this change just fine.

Would you expect the phage to tolerate these same modifications to p3?

1. C-terminal domain is required for release from the host cell following phage assembly, and contributes to structural stability of phage particle (See abstract http://chem.ps.uci.edu/~gweiss/WeissG-03JMB.pdf ). If we change the charge, it will alter intermolecular interactions, and it may destroy the functionality of p3, thus preventing the release of the phage and/or destabilizing the phage.

2. The codon sequence is not important as long as the appropriate amino acid is encoded, so the phage could tolerate this modification.

3. If the C-terminal is doubled in size, I think that it will still function normally, though it’s possible that it will not be able to pass through the P1-P4-P11 complex through which mature phage are secreted.

Would you expect the phage to tolerate transcriptional terminators that are 1. 2X stronger 2. 100X stronger 3. 2X weaker 4. 100X weaker ?

Assuming that we want the transcription to be stopped at a transcriptional terminator, it seems that it wouldn’t be a problem if the transcriptional terminator was stronger, unless an excessively strong transcriptional terminator caused the end part of the protein to be cut off. If a weak transcriptional terminator causes a protein to have a long tail that could potentially cause problems, should the tail undergo undesired intermolecular interactions of simply take up too much space in the phage. It may also be possible that a weak transcriptional terminator would not successfully stop translation of the protein, which would be a major problem.

The Family Tree: M13's closest evolutionary relatives

M13 is a bacteriophage in the family Inoviridae, known for being simple, circular single-stranded-DNA filamentous phage with very similar genetic design. Two of M13's closest relatives are bacteriophage fd and fl. Both of these phage differ from M13 slightly in their coats. M13 has an amide group of asparagine in position 12 whereas fd and fl have a carboxyl group of aspartate. (See http://www.wsu.edu/~hipps/pdf_files/phagep1.pdf ). "As a result of this difference, M13 has one negative charge less per subunit than fd, corresponding to a 25-30% reduction in surface charge density" (Tang et al., “Metal Ion-Induced Lateral Aggregation of Filamentous Viruses fd and M13”. http://www.biophysj.org/cgi/content/full/83/1/566 )

For further information on bacteriophage and a useful comparison of 12 different catergories of phage, see http://www.tulane.edu/~dmsander/WWW/224/Phages.html .