Team:Berkeley/Project/Payload

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Revision as of 00:56, 27 October 2010

Overview

"Payload" refers to the contents of a bacteria that are desired to be delivered to the cytoplasm of the Choanoflagellate. Payload can come in many forms: proteins, DNA, etc.

Green Fluorescent Protein Payload

In our Payload Delivery assay, we used green fluorescent protein (GFP) as our protein payload because it's delivery can be easily detected through use of fluorescent microscopy. To fill bacteria with our GFP payload, we transformed them with a plasmid containing our construct (INSERT NAME), which is GFP under a constitutive promoter. Then we turned them into delivery machines by transforming them again with our payload delivery device, fed these bacteria to Choanos, and induced lysis.

To see the results of this assay, visit our results page.

Targeted Fluorescent Protein Payload

In order to further confirm delivery, we delivered GFP fused to a nuclear localization tag {NLS) along with normal, untagged RFP. We hoped to observe Choanoflagellates that had a fluorescent red cytoplasm and had glowing green nuclei. However, we saw red and green throughout, meaning the NLS wasn't functional in Choanoflagellates.

Our future plans include trying other nuclear localization tags that have proven successful in other eukaryotes as well as constructing our own based off of BLASTs of the Choanoflagellate's genome for NLS-like sequences.

Plasmid Payload

Our delivery scheme also has the potential to deliver DNA. We currently are in the process of testing the delivery of several plasmids to the Choanoflagellates, some made by the King Lab and others by the Anderson lab. Most of the plasmids are pQXIN vectors with both SV40 and colE1 origins, and have eGFP under an animal promoter, such as Atub, Ef1a, and Myo. If the plasmids can be successfully delivered, replicated and expressed in the Choanoflagellates, they should glow green, allowing us to detect successful hits by using Flow Cytometry. This wasn't the case with our GFP delivery scheme, because there would be no way to distinguish Choanos that just ate fluorescent bacteria from successful delivery events. However, flow cytometry can be employed for Plasmid Payload, because the bacteria don't express the GFP on the plasmid they're delivering.

Transposase Payload

We're excited to take this project to the next level by delivering proteins that could make Choanoflagellates genetically tractable. Over the summer, we constructed a large portfolio of transposase parts and constructs. Transposases are enzymes capable of randomly cutting out pieces of DNA flanked by short terminal repeat sequences specific to that transposase and pasting them randomly into another stretch of DNA.

Our constructs contain the following three transposases:

1. Tn5
2. Sleeping Beauty
3. PiggyBac

Tn5

Tn5 transposase is native to E. Coli, but the wild-type protein expressed naturally by the cell is very inactive. Our version of Tn5 has been mutated to render it hyperactive. We added a nuclear localization tag to the Tn5 transposase, so that it would be transported to the Choano nucleus and insert its transposon into the Choano's genome.

Sleeping Beauty

Sleeping Beauty is a synthetic transposase that was made through ‘reverse engineering’ a defective copy of an ancestral Tc1/mariner-like transposase originally found in fish. Our version is SB100X, which is 100 times more active that the wildtype version. It contains an internal nuclear localization tag, so we didn't add an additional one.

PiggyBac

PiggyBac is transposase originally found in moths. Our version has been codon-optimized to work in mammalian cells. It contains an internal nuclear localization tag, so we didn't add an additional one.

The importance of Pre-pro's

We’ve also prefixed each transposase with a pre-pro, a sequence that targets proteins to the periplasm of the bacteria. This spatial barrier serves two purposes: it prevents the transposase from accesssing its transposon and inserting it into the bacteria’s genome instead of the Choano’s. Such an activity would be detrimental to the bacteria, since the transposon could be inserted into the middle of genes in the bacteria's chromosome, so the pre-pro acts to decrease toxicity of the transposases as well.