SynBioFromLeukipposInstitute

By Molly Michelson

"Remember those crazy-smart undergraduates we featured last year in our video about the international iGem competition? The competition challenges students to spend a summer coming up with synthetic biology solutions to problems and issues facing us in this 21st-century world.

http://bit.ly/1dZV1p1

by
Zachary Z. Sun, Clarmyra A. Hayes, Jonghyeon Shin, Filippo Caschera,  Richard M. Murray, Vincent Noireaux

"Ideal cell-free expression systems can theoretically emulate an in vivo cellular environment in a controlled in vitro platform.1 This is useful for expressing proteins and genetic circuits in a controlled manner as well as for providing a prototyping environment for synthetic biology.2,3 To achieve the latter goal, cell-free expression systems that preserve endogenous Escherichia coli transcription-translation mechanisms are able to more accurately reflect in vivo cellular dynamics than those based on T7 RNA polymerase transcription. We describe the preparation and execution of an efficient endogenous E. coli based transcription-translation (TX-TL) cell-free expression system that can produce equivalent amounts of protein as T7-based systems at a 98% cost reduction to similar commercial systems.4,5 The preparation of buffers and crude cell extract are described, as well as the execution of a three tube TX-TL reaction. The entire protocol takes five days to prepare and yields enough material for up to 3000 single reactions in one preparation. Once prepared, each reaction takes under 8 hr from setup to data collection and analysis. Mechanisms of regulation and transcription exogenous to E. coli, such as lac/tet repressors and T7 RNA polymerase, can be supplemented.6 Endogenous properties, such as mRNA and DNA degradation rates, can also be adjusted.7 The TX-TL cell-free expression system has been demonstrated for large-scale circuit assembly, exploring biological phenomena, and expression of proteins under both T7- and endogenous promoters.6,8 Accompanying mathematical models are available.9,10 The resulting system has unique applications in synthetic biology as a prototyping environment, or "TX-TL biomolecular breadboard.""

http://bit.ly/1dYet5r

 
http://bit.ly/1fDseL9

by
Dan Ferber

"How rare ‘words’ in bacterial genes make the difference

http://hvrd.me/16T1ZqN

http://bit.ly/198LEy0

You might remember the crowd funding campaign for CytoComp. This was done in the frame of a competition in the Startup Engineering MOOC class provided by Stanford University / Coursea. CytoComp won as the most funded project in this competition. I would like to thank all of you for your help and support. In addition to the money contribution, I really appreciate the awesome discussions we had, and all the new people I was lucky to get to know during the campaign.

Thanks to you all.

Here is the leader board:

http://bit.ly/14hsMkM

The home page for CytoComp here:

http://bit.ly/19BZYRK

An Introduction to Synthetic Biology
A One Day Course
San Francisco, October 12, 2013 http://bit.ly/16loOHe

An Introduction to Synthetic Biology
A One Day Course
San Francisco, October 12, 2013 http://bit.ly/16loOHe

by

Source: Rice University

"In the first study of its kind, Rice University scientists have used synthetic biology to study how a popular soil amendment called “biochar” can interfere with the chemical signals that some microbes use to communicate. The class of compounds studied includes those used by some plant pathogens to coordinate their attacks.

http://bit.ly/18GHaTh

 http://bit.ly/196WjPV

by
Xiaojie Duana, Tian-Ming Fub, Jia Liub, Charles M. Lieber

"Semiconductor nanowires configured as the active channels of field-effect transistors (FETs) have been used as detectors for high-resolution electrical recording from single live cells, cell networks, tissues and organs. Extracellular measurements with substrate supported silicon nanowire (SiNW) FETs, which have projected active areas orders of magnitude smaller than conventional microfabricated multielectrode arrays (MEAs) and planar FETs, recorded action potential and field potential signals with high signal-to-noise ratio and temporal resolution from cultured neurons, cultured cardiomyocytes, acute brain slices and whole animal hearts. Measurements made with modulation-doped nanoscale active channel SiNW FETs demonstrate that signals recorded from cardiomyocytes are highly localized and have improved time resolution compared to larger planar detectors. In addition, several novel three-dimensional (3D) transistor probes, which were realized using advanced nanowire synthesis methods, have been implemented for intracellular recording. These novel probes include (i) flexible 3D kinked nanowire FETs, (ii) branched intracellular nanotube SiNW FETs, and (iii) active silicon nanotube FETs. Following phospholipid modification of the probes to mimic the cell membrane, the kinked nanowire, branched intracellular nanotube and active silicon nanotube FET probes recorded full-amplitude intracellular action potentials from spontaneously firing cardiomyocytes. Moreover, these probes demonstrated the capability of reversible, stable, and long-term intracellular recording, thus indicating the minimal invasiveness of the new nanoscale structures and suggesting biomimetic internalization via the phospholipid modification. Simultaneous, multi-site intracellular recording from both single cells and cell networks were also readily achieved by interfacing independently addressable nanoprobe devices with cells. Finally, electronic and biological systems have been seamlessly merged in 3D for the first time using macroporous nanoelectronic scaffolds that are analogous to synthetic tissue scaffold and the extracellular matrix in tissue. Free-standing 3D nanoelectronic scaffolds were cultured with neurons, cardiomyocytes and smooth muscle cells to yield electronically-innervated synthetic or ‘cyborg’ tissues. Measurements demonstrate that innervated tissues exhibit similar cell viability as with conventional tissue scaffolds, and importantly, demonstrate that the real-time response to drugs and pH changes can be mapped in 3D through the tissues. These results open up a new field of research, wherein nanoelectronics are merged with biological systems in 3D thereby providing broad opportunities, ranging from a nanoelectronic/tissue platform for real-time pharmacological screening in 3D to implantable ‘cyborg’ tissues enabling closed-loop monitoring and treatment of diseases. Furthermore, the capability of high density scale-up of the above extra- and intracellular nanoscopic probes for action potential recording provide important tools for large-scale high spatio-temporal resolution electrical neural activity mapping in both 2D and 3D, which promises to have a profound impact on many research areas, including the mapping of activity within the brain."

http://bit.ly/14RYpzK

by

"Engineering of cell fate through synthetic gene circuits requires methods to precisely implement control around native decision-making pathways and offers the potential to direct developmental programs and redirect aberrantly activated cell processes. We set out to develop molecular network diverters, a class of genetic control systems, to activate or attenuate signaling through a mitogen-activated protein kinase (MAPK) pathway, the yeast mating pathway, to conditionally route cells to one of three distinct fates."

http://bit.ly/1fEoGps