User:Maerkl: Difference between revisions
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==Sebastian Maerkl== | ==Sebastian Maerkl== | ||
[[Image:picofme.jpg|left| | [[Image:picofme.jpg|left|110px]] | ||
Gradute Student<br> | Gradute Student<br> | ||
California Institute of Technology<br> | [http://www.caltech.edu California Institute of Technology]<br> | ||
Biochemistry and Molecular Biophysics Option<br> | [http://www.its.caltech.edu/~biochem/index.html Biochemistry and Molecular Biophysics Option]<br> | ||
===Contact Info=== | ===Contact Info=== | ||
Stanford University<br> | [http://www.stanford.edu Stanford University]<br> | ||
[http://bioengineering.stanford.edu Department of Bioengineering]<br> | |||
318 Campus Drive<br> | 318 Campus Drive<br> | ||
Clark Center, E300<br> | Clark Center, E300<br> | ||
| Line 12: | Line 13: | ||
email: maerkl@stanford.edu<br> | email: maerkl@stanford.edu<br> | ||
[http://thebigone.stanford.edu Quake Lab @ Stanford]<br> | [http://thebigone.stanford.edu Quake Lab @ Stanford]<br> | ||
===Research Interests=== | |||
My interests lie in solving problems in [http://en.wikipedia.org/wiki/Systems_biology Systems Biology] and [http://en.wikipedia.org/wiki/Proteomics Proteomics ]with the use of novel technology such as [http://en.wikipedia.org/wiki/Microfluidics Microfluidic] Large-Scale-Integration. | |||
Over the last half-decade I have helped develop MLSI in the laboratory of Prof. Quake at Stanford University. Prof. Quake's technology is based on using an elastomeric material called [http://en.wikipedia.org/wiki/Polydimethylsiloxane PDMS] to fabricate devices containing several layers of microfluidic channels using a technique termed multilayer soft lithography (MSL). With MSL it is possible to create structures that form functional micro-valves. Extending on this simple concept I designed the first LSI device containing thousands of valves in an area the size of a postage stamp. These early devices showed that it is possible to fabricate functional devices with almost arbitrary complexity with relative ease. Over the last several years I have been applying MLSI to solve problems in [http://en.wikipedia.org/wiki/Systems_biology Systems Biology] centered around performing protein biochemistry with greater ease and larger scale than can be accomplished with classical bench-top approaches. | |||
In particular I have been studying how basic-helix-loop-helix ([http://en.wikipedia.org/wiki/BHLH bHLH]) [http://en.wikipedia.org/wiki/Transcription_factor transcription factors] (TFs) recognize and bind to DNA. I established the first comprehensive binding energy landscape of a TF using a novel method for detecting interactions between molecules. This method is based on the mechanical induced trapping of molecular interactions (MITOMI) via a movable membrane. Establishing the exact modus operandi for any [http://en.wikipedia.org/wiki/Transcription_factor transcription factor] allows one to determine what genes it targets in vivo. This in turn allows one to not only establish transcriptional regulatory network topology but also the underlying parameters that drive the network, such as interaction strengths and dynamics of interacting nodes. | |||
I am also interested in applying MITOMI to various other forms of molecular interactions important in a cellular environment such as protein-protein and protein-RNA interactions. Studying protein-small molecule interactions on the other hand will be useful in screening potential pharmaceuticals in high-throughput. | |||
===Gallery=== | ===Gallery=== | ||
<gallery> | <gallery> | ||
Image:sciencecover.gif|The first microfluidic device containing thousands of valves. | Image:sciencecover.gif|The first microfluidic device containing thousands of valves. | ||
Image: | Image:DTPA_nextgen.bmp|Subsection of a microfluidic device showing the complex network of channels. | ||
Image:MITOMI_close.jpg|Subset of MITOMI unit cells used to take precise measurements of molecular interactions on a microfluidic device. | |||
</gallery> | </gallery> | ||
| Line 29: | Line 36: | ||
<blockquote> | <blockquote> | ||
<biblio> | <biblio> | ||
#1 | #1 pmid=17218526 | ||
#2 pmid=12351675 | #2 pmid=12351675 | ||
</biblio> | </biblio> | ||
Latest revision as of 18:45, 16 January 2007
Sebastian Maerkl
Gradute Student
California Institute of Technology
Biochemistry and Molecular Biophysics Option
Contact Info
Stanford University
Department of Bioengineering
318 Campus Drive
Clark Center, E300
Stanford, CA 94305
email: maerkl@stanford.edu
Quake Lab @ Stanford
Research Interests
My interests lie in solving problems in Systems Biology and Proteomics with the use of novel technology such as Microfluidic Large-Scale-Integration.
Over the last half-decade I have helped develop MLSI in the laboratory of Prof. Quake at Stanford University. Prof. Quake's technology is based on using an elastomeric material called PDMS to fabricate devices containing several layers of microfluidic channels using a technique termed multilayer soft lithography (MSL). With MSL it is possible to create structures that form functional micro-valves. Extending on this simple concept I designed the first LSI device containing thousands of valves in an area the size of a postage stamp. These early devices showed that it is possible to fabricate functional devices with almost arbitrary complexity with relative ease. Over the last several years I have been applying MLSI to solve problems in Systems Biology centered around performing protein biochemistry with greater ease and larger scale than can be accomplished with classical bench-top approaches.
In particular I have been studying how basic-helix-loop-helix (bHLH) transcription factors (TFs) recognize and bind to DNA. I established the first comprehensive binding energy landscape of a TF using a novel method for detecting interactions between molecules. This method is based on the mechanical induced trapping of molecular interactions (MITOMI) via a movable membrane. Establishing the exact modus operandi for any transcription factor allows one to determine what genes it targets in vivo. This in turn allows one to not only establish transcriptional regulatory network topology but also the underlying parameters that drive the network, such as interaction strengths and dynamics of interacting nodes.
I am also interested in applying MITOMI to various other forms of molecular interactions important in a cellular environment such as protein-protein and protein-RNA interactions. Studying protein-small molecule interactions on the other hand will be useful in screening potential pharmaceuticals in high-throughput.
Gallery
-
The first microfluidic device containing thousands of valves.
-
Subsection of a microfluidic device showing the complex network of channels.
-
Subset of MITOMI unit cells used to take precise measurements of molecular interactions on a microfluidic device.
Publications
- Maerkl SJ and Quake SR. A systems approach to measuring the binding energy landscapes of transcription factors. Science. 2007 Jan 12;315(5809):233-7. DOI:10.1126/science.1131007 |
- Thorsen T, Maerkl SJ, and Quake SR. Microfluidic large-scale integration. Science. 2002 Oct 18;298(5593):580-4. DOI:10.1126/science.1076996 |
Patents
- Maerkl S.J. and S.R. Quake, ``Programming Microfluidic Devices with Molecular Information, # 60/762,344.
- Maerkl S.J. and S.R. Quake, ``Mechanically Induced Trapping of Molecular Interactions, # 60/762,300.
- Maerkl S.J., Thorsen T., Bao X., Quake, S.R. and Studer V., ``Microfluidic Large Scale Integration, # WO2004028955.
