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University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

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Page 1: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF
Page 2: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

University of Wisconsin-Madison Team MembersNathan Klapoetke

Sean McMasterDavid Peterson

ATF

Page 3: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Our Vision

Page 4: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Interface Criteria

Modular design Compatible with bacterial and

mammalian systems Well characterized Reliable

Page 5: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

What is ATF?

1) DNA binding domain (DBD), recognizes specific DNA sequence and binds to it

2) Effector domain (ED), recruits cellular machinery to site where DBD has bound

DBD

ED

++ or - -

Zinc finger

Activate or repress gene transcription

Page 6: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Zinc Finger

Made of 30 amino acids Chelated by 1 zinc ion Protein structure (beta-beta-alpha)

Page 7: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Zinc Finger

Recognizes 3 base pairs of DNA Alpha-helix interacts with the

DNA triplet Some fingers can recognize 4

base pairs Can covalently link fingers to

recognize and bind to longer DNA sequence. Greatly increases DNA binding

specificity

*5

Page 8: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

ATFα

Obtained from Carlos Barbas III Binds to GGA-GTT-G** 3 zinc fingers are

linked by TGEKP Has transcription

factor VP64, a strong activator

Original Zif extracted from pMX plasmid

Page 9: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

ATFΩ

Reformatting of ATFα Cloning Site-directed mutagenesis Analysis

Design is specific to the Bcl-2 promoter Exploited in subsequent experiments

Page 10: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Cloning

5000

6000

500

5000

500

6000

5000

6000

Digestion of Clones

Page 11: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Mutagenesis

Changing amino acids to conform to ideal binding sites (*1, *2)

Page 12: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Existing ZiF Design Tools

Based on meta-analysis of the “GNN” family Zif (*1, *2)

Page 13: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

ATFΩ

Page 14: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Limitations of ZiF Tools

Cannot accurately predict binding effects of covalently linked zinc fingers

Does not give binding affinity Cannot screen for additional undesired

binding sequences

Page 15: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Cognate Site Identity (CSI) Array

•Unbiased

•Probe entire N-mer sequence space

*3

Page 16: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

9-mer Array1nM ZiF1:1000 HA antibody1x HOX50uM Zinc Acetate0.01% Triton X

CW115-IG9mer array

Page 17: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF
Page 18: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Binding Affinity

Page 19: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Position Weight Matrix

*4

Page 20: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

ATF test system

Page 21: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Why regulate Bcl-2?

“… manipulation of the Bcl-2 system may also provide new treatments to forestall cardio-myocyte apoptosis. The potential strategies could involve up-regulating the antiapoptotic Bcl-2 …” -Gill, Mestril, and Samali, 2002

“Antiapoptotic Bcl-2 proteins have therapeutic potential for heart disease, since they have been shown to protect myocardial cells from various stresses.”-Gustafsson and Gottlieb, 2007

“… balancing Bcl-2 to Bax in transplanted hearts promotes long-term graft survival.” -Tung et al., 2003

Page 22: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Bcl-2 Regulation

Oxidative stress (such as caused by Doxorubicin) induces apoptosis

ATFΩ is designed to inhibit apoptosis

Page 23: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

ATF in action

*Assay for function in mouse cells

Page 24: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Western Blot Results

Probing for presence of ATF:

Probing for change in Bcl-2 protein levels: vector vector ATF ATF +TET +TET

ATF ATF vector (-) ctrl+TET

} ~23kd

} ~26kd

Page 25: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Future in vivo testing

Work in bacteria, Mammalian cells are complicated

Target a different pathway Bcl-2 family of proteins are complicated

Page 26: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Conclusion

So, since we have begun, questions may have been created more questions than they have been answered. But, the ideas and possibilities that come from harnessing ATF technology was well worth it.

Page 27: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

References 1. GNN Dreier B, Segal DJ, Barbas CF 3rd. Insights into the molecular recognition of

the 5'-GNN-3' family of DNA sequences by zinc finger domains. J Mol Biol. 2000 Nov 3;303(4):489-502.

2. GNN Segal DJ, Dreier B, Beerli RR, Barbas CF 3rd. Toward controlling gene expression at will: selection and design of zinc finger domains recognizing each of the 5'-GNN-3' DNA target sequences. Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2758-63.

3. C. L. Warren et al. 2005. Defining the sequence-recognition profile of DNA-binding molecules. Proc. Natl. Acad. Sci. USA. 103: 867-872.

4. Crooks, Gavin et al. 2004. WebLogo: A Sequence Logo Generator. Genome Res. 14:1188-1190.

5. Luscombe, Nicholas, et al (9 June 2000). "An overview of the structures of protein-DNA complexes." Genome Biology Review 1 (1): 4-5.

6. Serebriiskii et al., 2007 7. Adams and Cory, 2001 8. Torsten Wittman, UCSF

Page 28: University of Wisconsin-Madison Team Members Nathan Klapoetke Sean McMaster David Peterson ATF

Thanks

Advisors: Aseem Ansari, Franco Cerrina, & Doug Weibel

We would like to thank the following people for their suggestions and aid in the implementation of this project: Clayton Carlson, Leslie Donato, Chris Warren,

Mary Ozers

We would like to thank the College of Engineering, Nanoscale Science and Engineering Center, and Chancellor John Wiley for their financial support.