Tissue, I hardly know you!

== FINAL PPT (without periostin section) [1]

==

20.20 Tissue Engineering Group

• Group members: Anna, Amber, Derek, Prarthna, Mike, Robbie, and Aditya

Use this space to communicate with each othhttp://openwetware.org/skins/common/images/button_extlink.pnger and to formulate your ideas. Here's a link to the technical specification review requirements([2]).

PLAN OF TASKS:

--periostin part on registry /n --research safety and security /n --bactoblood /n --antibodies on heart/n --binding/n --finalize pathways from binding to NAND gates/n --6 month plan /n --competition/n --costs (as part of 6 month plan)/n --finalize collagenase part

Devices:

1. targeting mechanism (specific for heart scar tissue)
2. propulsion device (might not be necessary if we just let the cells travel with blood flow)
3. binding device
4. scar-digesting device
5. healthy heart cell regeneration device
6. cell death / exit device

IMPORTANT!! Project Log!

Hey, my roommate says the project log is a group thing. I'm not sure if that's right, but if it is, we should get together and work that out.

Perisotin Gene Sequence

http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&id=5453833 cytogenic coordinates 13q13.3]

[3]

[useful articles that discuss proteins expressed in cardiac scar and healthy tissue and how the two tissues differ.] [4]

[Periostin and Myocardial Repair, Regeneration, and Recovery [5]]

The main inspiring project. http://www.childrenshospital.org/newsroom/Site1339/mainpageS1339P1sublevel319.html

[Document of gene sequence of periostin device]

   http://openwetware.org/wiki/Image:Periostin_DNA_sequence.doc

[Summary of research on targeting scar heart tissue as well as binding to healthy and scarred cardiac cells. Also includes a summary of monoclonal antibody production and a diagram of the cardiac extracellular matrix (useful for figuring out how our bacterium will bind to it). ]

POWERPOINT FOR TECH SPEC REVIEW

[6]

TOPICS FOR ADDITIONAL RESEARCH: 1. Do we keep the bacteria in the heart until they die, or do we inject the patient with a drug to end the bacteria's life cycle.

  - research the life span of the bacteria
  - how would the bacteria behave when they die? Do they automatically unbind from the cell  or are external factors necessary. 

2. Ways to prevent the immune system from responding to the bacteria

  -could a coating be synthesized to prevent bacterial death and to prevent an immune system response. 

3. Will Verapamil (the scar repressing agent) interact with periostin?

4. How quickly does cardiac tissue form?

  - If it forms slowly relative to the speed at which periostin regenerates heart tissue, it is not necessary to include scar repressors.

Competition/ Other research being done

Lepilina A, Coon AN, Kikuchi K, Holdway JE, Roberts RW, Burns CG, et al. A dynamic epicardial injury response supports progenitor cell activity during zebrafish heart regeneration. Cell 2006;127(3):607–19.

Lien CL, Schebesta M, Makino S,Weber GJ,KeatingMT. Gene expression analysis of zebrafish heart regeneration. PLoS Biol 2006;4(8):e260.

[POWERPOINT TECH SPEC]

File:Technical Specification Review.ppt

PRELIMINARY 6 MONTH PLAN

[7]

TECHNICAL DOCUMENTATION, ROUGH DRAFT

File:Final Presentation-Technical Documentation.doc

Robbie's edits http://openwetware.org/wiki/Image:Final_Presentation-Technical_Documentation_Robbieedits.doc

Final Technical Documenation File:Technical Documentation-Final Version.doc

Amber's edits: http://openwetware.org/wiki/Image:Technical_Documentation-Final_Version-amber_edits.doc

PARTS

BBa_I728950 - Periostin Sequence

BBa_I728951 - Collagenase

DIAGRAMS

File:C:\Users\Anna Shcherbina\Pictures\DSCF2071.jpg File:C:\Users\Derek Ju\Pictures\collagenase.jpg

PROTEIN SECRETION

http://www.freepatentsonline.com/5223407.html