Team:Berkeley Wetlab/Automation

From 2009.igem.org

Revision as of 20:01, 19 October 2009 by Jennbrophy (Talk | contribs)

Contents

Why Automate?

Our approach to characterizing cell surface display required us to make a lot of parts. Without an automated mode of assembly it would not be possible for us to make enough parts to characterize cell surface display with a combinatorial method.

Making Basic Parts

Making basic parts is the first step toward making any synthetic biology device. Making basic parts typically entails mixing oligo nucleotides and with template DNA and doing PCR, or doing PCR with many complimentary oligos to . Our team needed to make a lot of basic parts, so we developed a method for doing cheap in-house gene synthesis.

Making Composite Parts

The next step, after making new basic parts, is to assemble those basic parts into composite part devices. There has been a lot of work being done at UC Berkeley to automate the process of composite part assembly. We were able to implement many newly developed techniques to create a large number of composite parts.

Two AntiBiotic Assembly

BerkeleyAssembly.png

Clonebots

Clotho

Success!

Using our newly developed automated assembly processes we were able to make over 800 parts (both basic and composite) in one summer! This magnitude of part making is unprecedented in iGEM competitions and enabled us to test a very large number of variations on cell surface display systems.

Success Rates

The assembly scheme we developed works just as well as assembly by hand and is much faster.

BerkeleyAssemblyScheme.jpg We made a lot of parts with a robot.