SynBioFromLeukipposInstitute
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Scooped by Gerd Moe-Behrens
January 5, 2013 1:12 PM
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Towards a bottom-up reconstitution of bacterial cell division

Towards a bottom-up reconstitution of bacterial cell division | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Ariadna Martos, Mercedes Jiménez, Germán Rivas, Petra Schwille

"The components of the bacterial division machinery assemble to form a dynamic ring at mid-cell that drives cytokinesis. The nature of most division proteins and their assembly pathway is known. Our knowledge about the biochemical activities and protein interactions of some key division elements, including those responsible for correct ring positioning, has progressed considerably during the past decade. These developments, together with new imaging and membrane reconstitution technologies, have triggered the ‘bottom-up’ synthetic approach aiming at reconstructing bacterial division in the test tube, which is required to support conclusions derived from cellular and molecular analysis. Here, we describe recent advances in reconstituting Escherichia coli minimal systems able to reproduce essential functions, such as the initial steps of division (proto-ring assembly) and one of the main positioning mechanisms (Min oscillating system), and discuss future perspectives and experimental challenges."

http://bit.ly/TD7d6I

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January 5, 2013 12:51 PM
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Synthetic multicellularity

Synthetic multicellularity | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Michel M. Maharbiz

"The ability to synthesize biological constructs on the scale of the organisms we observe unaided is probably one of the more outlandish, yet recurring, dreams humans have had since they began to modify genes. This review brings together recent developments in synthetic biology, cell and developmental biology, computation, and technological development to provide context and direction for the engineering of rudimentary, autonomous multicellular ensembles."

http://bit.ly/UNps9w

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January 5, 2013 12:14 PM
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*Wikigenes* *Synthetic Biology*

*Wikigenes* *Synthetic Biology* | SynBioFromLeukipposInstitute | Scoop.it
The world's first wiki where authorship really matters. Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts.
Gerd Moe-Behrens's insight:

WikiGenes - Collaborative Publishing 

This is a really great resource, where you can find a lot of SynBio material.
The great thing: It is created by the community and for the community. Fell free to join and add your contribution.

http://bit.ly/wlk5vu

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Scooped by Gerd Moe-Behrens
January 4, 2013 8:06 AM
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Opportunities for Synthetic Biology in Antibiotics: Expanding Glycopeptide Chemical Diversity

Opportunities for Synthetic Biology in Antibiotics: Expanding Glycopeptide Chemical Diversity | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Maulik N. Thaker and Gerard D. Wright

"Synthetic biology offers a new path for the exploitation and improvement of natural products to address the growing crisis in antibiotic resistance. All antibiotics in clinical use are facing eventual obsolesce as a result of the evolution and dissemination of resistance mechanisms, yet there are few new drug leads forthcoming from the pharmaceutical sector. Natural products of microbial origin have proven over the past 70 years to be the wellspring of antimicrobial drugs. Harnessing synthetic biology thinking and strategies can provide new molecules and expand chemical diversity of known antibiotic scaffolds to provide much needed new drug leads. The glycopeptide antibiotics offer paradigmatic scaffolds suitable for such an approach. We review these strategies here using the glycopeptides as an example and demonstrate how synthetic biology can expand antibiotic chemical diversity to help address the growing resistance crisis...."
http://bit.ly/Uo8PPa

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January 4, 2013 7:33 AM
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Synthetic biology strategies for synthesizing polyhydroxyalkanoates from unrelated carbon sources

Synthetic biology strategies for synthesizing polyhydroxyalkanoates from unrelated carbon sources | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Daniel E. Agnewa, Brian F. Pflegera

"iscovered in the 1920’s, polyhydroxyalkanoates (PHA) are a naturally occurring class of biopolyestersthat have long been touted as a renewable, biodegradable plastic alternative. Demand for sustainable products and over a half century of research have led to moderate commercial success of PHA. Yet, these materials are not pervasive. Therefore, an important question to address is, “what is the barrier that prevents widespread application of these materials?” PHA can be made from an incredibly diverse class of monomers that incorporate both simple and complex organic acids. Herein, we provide an updated list of unique PHA monomers that are substrates for a PHA polymerase. Unfortunately, most unique monomers are incorporated only after feeding a structurally related feedstock to a PHA accumulating bacterium.Therefore, we put forward an argument that research must now turn to developing feedstock-independent, synthetic pathways to producean increased diversity of PHAs capable of competing withpetroleum-derived plastics.

 Highlights► A list of 64 new and unique PHA monomers identified since 1995 was compiled. ► An argument was made for accessing novel monomers by avoiding related feedstocks. ► Review of known and potential pathways for making monomers from unrelated sources. ► Synthetic biology and its impact on metabolic engineering was discussed."


 http://bit.ly/UKINbr

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Scooped by Gerd Moe-Behrens
January 3, 2013 7:40 PM
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Genomic variation landscape of the human gut microbiome

Genomic variation landscape of the human gut microbiome | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Siegfried Schloissnig,Manimozhiyan Arumugam,Shinichi Sunagawa,Makedonka Mitreva, Julien Tap,Ana Zhu,Alison Waller,Daniel R. Mende,Jens Roat Kultima,John Martin, Karthik Kota,Shamil R. Sunyaev,George M. Weinstock& Peer Bork

"Whereas large-scale efforts have rapidly advanced the understanding and practical impact of human genomic variation, the practical impact of variation is largely unexplored in the human microbiome. We therefore developed a framework for metagenomic variation analysis and applied it to 252 faecal metagenomes of 207 individuals from Europe and North America. Using 7.4 billion reads aligned to 101 reference species, we detected 10.3 million single nucleotide polymorphisms (SNPs), 107,991 short insertions/deletions, and 1,051 structural variants. The average ratio of non-synonymous to synonymous polymorphism rates of 0.11 was more variable between gut microbial species than across human hosts. Subjects sampled at varying time intervals exhibited individuality and temporal stability of SNP variation patterns, despite considerable composition changes of their gut microbiota. This indicates that individual-specific strains are not easily replaced and that an individual might have a unique metagenomic genotype, which may be exploitable for personalized diet or drug intake."

http://bit.ly/10W4SIr

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January 3, 2013 2:44 PM
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Genetic Literacy Project

Genetic Literacy Project | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

"Mission:

Genetics is our future. It can be a source of dramatic innovations to improve food security, the environment and public health. In theory, biotechnology and related cutting edge sciences are widely celebrated. But in practice, the words “gene” and “genetic engineering” often stir fear and misunderstanding. Intricate science scares people who don’t understand risk and complexity. What is the potential of agricultural and human genetics? The goal of the GLP is to serve as a resource to those interested in disentangling ideology from science. The GLP is non-partisan non-profit organization funded by donations from various philanthropies. It is affiliated with the non-profit Statistical Assessment Service (STATS) based at George Mason University in Virginia."


http://bit.ly/UJd2Q2

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January 3, 2013 2:29 PM
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Synthetic polymers and their potential as genetic materials

Gerd Moe-Behrens's insight:

by
Pinheiro VB, Loakes D, Holliger P.

"DNA and RNA are the only known natural genetic materials. Systematic modification of each of their chemical building blocks (nucleobase, sugar, and phosphate) has enabled the study of the key properties that make those nucleic acids genetic materials. All three moieties contribute to replication and, significantly, all three moieties can be replaced by synthetic analogs without loss of function. Synthetic nucleic acid polymers capable of storing and propagating information not only expand the central dogma, but also highlight that DNA and RNA are not unique chemical solutions for genetic information storage. By considering replication as a question of information transfer, we propose that any polymer that can be replicated could serve as a genetic material. Editor's suggested further reading in BioEssays Xenobiology: A new form of life as the ultimate biosafety tool Abstract."

http://bit.ly/UJbJ3B

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January 2, 2013 4:53 PM
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George Church Will look to Human Genetic outliers and Transgenic sources to improve Humans

George Church Will look to Human Genetic outliers and Transgenic sources to improve Humans | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

http://bit.ly/W38DUS

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January 2, 2013 4:20 PM
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Stable Gene Targeting in Human Cells Using Single-Strand Oligonucleotides with Modified Bases

Stable Gene Targeting in Human Cells Using Single-Strand Oligonucleotides with Modified Bases | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by

Xavier Rios, Adrian W. Briggs, Danos Christodoulou, Josh M. Gorham, Jonathan G. Seidman, George M. Church 

"Recent advances allow multiplexed genome engineering in E. coli, employing easily designed oligonucleotides to edit multiple loci simultaneously. A similar technology in human cells would greatly expedite functional genomics, both by enhancing our ability to test how individual variants such as single nucleotide polymorphisms (SNPs) are related to specific phenotypes, and potentially allowing simultaneous mutation of multiple loci. However, oligo-mediated targeting of human cells is currently limited by low targeting efficiencies and low survival of modified cells. Using a HeLa-based EGFP-rescue reporter system we show that use of modified base analogs can increase targeting efficiency, in part by avoiding the mismatch repair machinery. We investigate the effects of oligonucleotide toxicity and find a strong correlation between the number of phosphorothioate bonds and toxicity. Stably EGFP-corrected cells were generated at a frequency of ~0.05% with an optimized oligonucleotide design combining modified bases and reduced number of phosphorothioate bonds. We provide evidence from comparative RNA-seq analysis suggesting cellular immunity induced by the oligonucleotides might contribute to the low viability of oligo-corrected cells. Further optimization of this method should allow rapid and scalable genome engineering in human cells."  

 http://bit.ly/MbNeVW

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January 1, 2013 12:35 PM
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Science Topics Find an Audience in Social Media

Science Topics Find an Audience in Social Media | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
MARY ANN GIORDANO

"The largest and most sophisticated rover landed safely on Mars and the world’s most famous Moon visitor died, but the space event that most captured the public’s imagination in 2012 involved a journey to Earth.

On Oct. 14, YouTube counted 52 million streams of the Austrian daredevil Felix Baumgartner’s supersonic, record-breaking jump from a balloon 24 miles above the New Mexico desert. YouTube called it “one of the most-viewed live events ever,” and it landed at No. 10 on the video-sharing site’s year-end trending list — the first time a science-related subject made the list, a YouTube spokeswoman said. (Google listed the leap as No. 7 in its Zeitgeist 2012 of trending events.)

And it was far from the only science story to go viral. To put it in 140 characters or less, social media and science found each other in 2012.

In surprising numbers, people posted, viewed and searched for science-related topics last year — sharing news from space and undersea, commenting on new discoveries and uploading photos and video in a full-out embrace of the ability to communicate with thousands of others about global subjects in real time.

The first Twitter message on Aug. 5 from @MarsCuriosity, NASA’s official rover handle — “Gale Crater I Am in You!!!” — was retweeted more than 72,000 times. Photos of the space shuttle Endeavour flying over the West Coast, on its way to its final resting place, ricocheted across the planet. And the director James Cameron’s claim to have sent the “deepest tweet” — from the Mariana Trench, about seven miles below the surface of the Pacific — was rated one of Twitter’s “moments of serendipity and just plain awesomeness” (though it was actually sent by a friend above water). Four science-related events made that list, with the Mars landing at No. 1.In an age of despair over math and science acuity, it appears that what was once considered uninteresting or unfathomable has become cool and exciting.
......"
http://nyti.ms/WYurni

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December 30, 2012 12:43 PM
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Submicrometre geometrically encoded fluorescent barcodes self-assembled from DNA

Submicrometre geometrically encoded fluorescent barcodes self-assembled from DNA | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:
byChenxiang Lin, Ralf Jungmann, Andrew M. Leifer, Chao Li, Daniel Levner,George M. Church, William M. Shih & Peng Yin

"The identification and differentiation of a large number of distinct molecular species with high temporal and spatial resolution is a major challenge in biomedical science. Fluorescence microscopy is a powerful tool, but its multiplexing ability is limited by the number of spectrally distinguishable fluorophores. Here, we used (deoxy)ribonucleic acid (DNA)-origami technology to construct submicrometre nanorods that act as fluorescent barcodes. We demonstrate that spatial control over the positioning of fluorophores on the surface of a stiff DNA nanorod can produce 216 distinct barcodes that can be decoded unambiguously using epifluorescence or total internal reflection fluorescence microscopy. Barcodes with higher spatial information density were demonstrated via the construction of super-resolution barcodes with features spaced by ∼40 nm. One species of the barcodes was used to tag yeast surface receptors, which suggests their potential applications as in situ imaging probes for diverse biomolecular and cellular entities in their native environments."


http://bit.ly/Vq2d69
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December 29, 2012 3:22 PM
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‘Shotgun DNA synthesis’ for the high-throughput construction of large DNA molecules

‘Shotgun DNA synthesis’ for the high-throughput construction of large DNA molecules | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Hwangbeom Kim, Hyojun Han, Jinwoo Ahn, Joongoo Lee, Namjin Cho, Hoon Jang, Hyoki Kim, Sunghoon Kwon, and Duhee Bang

"We developed a highly scalable ‘shotgun’ DNA synthesis technology by utilizing microchip oligonucleotides, shotgun assembly and next-generation sequencing technology. A pool of microchip oligonucleotides targeting a penicillin biosynthetic gene cluster were assembled into numerous random fragments, and tagged with 20bp degenerate barcode primer pairs. An optimal set of error-free fragments were identified by high-throughput DNA sequencing, selectively amplified using the barcode sequences, and successfully assembled into the target gene cluster...."

http://1.usa.gov/UAxLqd

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January 5, 2013 1:05 PM
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Designer nucleic acids to probe and program the cell

Designer nucleic acids to probe and program the cell | SynBioFromLeukipposInstitute | Scoop.it
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by

Yamuna Krishnan, Mark Bathe "Recent advances in nucleic acid sequencing, structural, and computational technologies have resulted in dramatic progress in our understanding of nucleic acid structure and function in the cell. This knowledge, together with the predictable base-pairing of nucleic acids and powerful synthesis and expression capabilities now offers the unique ability to program nucleic acids to form precise 3D architectures with diverse applications in synthetic and cell biology. The unique modularity of structural motifs that include aptamers, DNAzymes, and ribozymes, together with their well-defined construction rules, enables the synthesis of functional higher-order nucleic acid complexes from these subcomponents. As we illustrate here, these highly programmable, smart complexes are increasingly enabling researchers to probe and program the cell in a sophisticated manner that moves well beyond the use of nucleic acids for conventional genetic manipulation alone...." http://bit.ly/TRdxXg ;
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January 5, 2013 12:35 PM
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Synthetic Biology

Synthetic Biology | SynBioFromLeukipposInstitute | Scoop.it
Welcome to World University which anyone can add to or edit. The Global, Virtual/Digital, Open...
Gerd Moe-Behrens's insight:

*World University*
*Synthetic Biology*

A new open course initiative!

http://bit.ly/Wvs49G

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January 4, 2013 8:33 AM
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Bioprinting for stem cell research

Bioprinting for stem cell research | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Savas Tasog, Utkan Demirci

"Recently, there has been growing interest in applying bioprinting techniques to stem cell research. Several bioprinting methods have been developed utilizing acoustics, piezoelectricity, and lasers to deposit living cells onto receiving substrates. Using these technologies, spatially defined gradients of immobilized biomolecules can be engineered to direct stem cell differentiation into multiple subpopulations of different lineages. Stem cells can also be patterned in a high-throughput manner onto flexible implementation patches for tissue regeneration or onto substrates with the goal of accessing encapsulated stem cells of interest for genomic analysis. Here, we review recent achievements with bioprinting technologies in stem cell research, and identify future challenges and potential applications including tissue engineering and regenerative medicine, wound healing, and genomics."

http://bit.ly/133mJN8

Phillip Trotter's curator insight, January 5, 2013 6:33 AM

As usual wonderful link from Socrates Logos. If you have seen press release coverage on companies such as Autodesk researching 3D printers for biology then this article explains a lot of the background concepts and technologies. Worth reading.

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January 4, 2013 8:00 AM
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Why Accurate Human Embryology Is Needed To Evaluate Current Trends In Research Involving Stem Cells, Genetic Engineering, Synthetic Biology and Nanotechnology

Gerd Moe-Behrens's insight:

by
Dianne N. Irving 

"When does a new living human being begin to exist? This is an important scientific question these days, as much research -- including stem cell research, cloning, genetic engineering, synthetic biology, nanotechnology, etc. -- is performed using the early human embryo, and should be the starting point for any ethical analyses. But the answer to that scientific question depends on whether the human being was sexually or asexually reproduced.

Either way, once that new human being begins to exist, his/her rights should be fully respected and should be protected from harm -- ethically, legally and politically -- just as any other human being should be. Right? Even the European Court of Justice recently decided that both sexually and asexually reproduced human beings cannot be destroyed in scientific research for purposes of patents.1Many of the objective scientific facts needed to understand both sexual and asexual human reproduction, and when human beings reproduced by these techniques begin to exist, are found in the Carnegie Stages of Early Human Embryonic Development. Quite unfortunately, this most universally accepted and documented source of such objective scientific information since 1942 (and continuously updated since then) has changed the URLs for its documentation online (although the same information is available in hard cover). This means that readers who need the accurate science and want to study the original documentation can no longer find that online by simply using the URLs found in any articles, books, etc., written over the last 40 years. And given that the early human embryo -- whether sexually or asexually reproduced -- is now involved in new complicated basic and medical research, as well as addressed in legal and ideological issues never even before contemplated, it is more important than ever to get this science straight in order that the ethical issues involved can be legitimately evaluated.The purpose of this article, then, is to provide the readers with these new online URLs for the Carnegie Stages, and quote directly from them concerning the documentation of both sexual and asexual human reproduction. It is hoped that such accurate objective scientific facts can help to dispel at least some of the multitude of "scientific myths" surrounding these issues so prolific in these current debates -- especially given the current exponential rise in scientific fraud.2 Be sure to file them somewhere for easy access in order to verify the accuracy of scientific "claims" in the literature. Extensive references are also provided to familiarize the readers with current trends (most of which, interestingly, overlap)...." 

 http://bit.ly/Z2zpPA

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January 4, 2013 7:27 AM
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Characterization of a quorum sensing device for synthetic biology design: Experimental and modeling validation

Characterization of a quorum sensing device for synthetic biology design: Experimental and modeling validation | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Nazanin Saeidi, Mohamed Arshath, Matthew Wook Chang, Chueh Loo Poh

"Modeling of biological parts is of crucial importance as it enables the in silico study of synthetic biological systems prior to the actual construction of genetic circuits, which can be time consuming and costly. Because standard biological partsare utilized to build the synthetic systems, it is important that each of these standard parts is well characterized and has a corresponding mathematical model that could simulate the characteristics of the part. These models could be used in computer aided design (CAD)tools during the design stage to facilitate the building of the model of biological systems. Thispaperdescribes the development of a mathematical model that is able to simulate both the dynamic and static performance of a biological device created using standard parts. We modeled an example quorum sensing device that produces green fluorescent protein (GFP) as reporter in the presence ofAcyl Homoserine Lactone (AHL). The parameters of the model were estimated using experimental results. The simulation results show that the model was able to simulate behavior similar to experimental results. Since it is important that these models and the content in the models can be searchable and readable by machines, standard SBML (system biology markup language) format was used to store the models. All parts and reactions are fully annotated to enable easy searching, and the models follow the Minimum Information Requested In the Annotation of Models (MIRIAM) compliance as well as the Minimum Information About a Simulation Experiment (MIASE).

 Highlights► We developed mathematical model that simulates dynamic and static performance of a biological device. ► We modeled an example quorum sensing device that produces GFP in the presence of AHL. ► The simulation results show that the model was able to simulate behavior similar to experimental results. ► Standard SBML (system biology markup language) format was used to store the model. ► The model follows the MIRIAM and MIASE compliances"


http://bit.ly/VmMtPb

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January 3, 2013 2:54 PM
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Multiplex Genome Engineering Using CRISPR/Cas Systems

Multiplex Genome Engineering Using CRISPR/Cas Systems | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by
Le Cong, F. Ann Ran, David Cox, Shuailiang Lin, Robert Barretto, Naomi Habib, Patrick D. Hsu, Xuebing Wu, Wenyan Jiang, Luciano Marraffini, Feng Zhang

"Functional elucidation of causal genetic variants and elements requires precise genome editing technologies. The type II prokaryotic CRISPR (clustered regularly interspaced short palindromic repeats) adaptive immune system has been shown to facilitate RNA-guided site-specific DNA cleavage. We engineered two different type II CRISPR systems and demonstrate that Cas9 nucleases can be directed by short RNAs to induce precise cleavage at endogenous genomic loci in human and mouse cells. Cas9 can also be converted into a nicking enzyme to facilitate homology-directed repair with minimal mutagenic activity. Finally, multiple guide sequences can be encoded into a single CRISPR array to enable simultaneous editing of several sites within the mammalian genome, demonstrating easy programmability and wide applicability of the CRISPR technology..."
http://bit.ly/RvcPjN

comment in MIT news:
*Editing the genome with high precision* 

by
Anne Trafton

"Researchers at MIT, the Broad Institute and Rockefeller University have developed a new technique for precisely altering the genomes of living cells by adding or deleting genes. The researchers say the technology could offer an easy-to-use, less-expensive way to engineer organisms that produce biofuels; to design animal models to study human disease; and  to develop new therapies, among other potential applications.

 To create their new genome-editing technique, the researchers modified a set of bacterial proteins that normally defend against viral invaders. Using this system, scientists can alter several genome sites simultaneously and can achieve much greater control over where new genes are inserted, says Feng Zhang, an assistant professor of brain and cognitive sciences at MIT and leader of the research team.   “Anything that requires engineering of an organism to put in new genes or to modify what’s in the genome will be able to benefit from this,” says Zhang, who is a core member of the Broad Institute and MIT’s McGovern Institute for Brain Research. Zhang and his colleagues describe the new technique in the Jan. 3 online edition of Science. Lead authors of the paper are graduate students Le Cong and Ann Ran....."


http://bit.ly/XnultA ;

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January 3, 2013 2:35 PM
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Opportunities for protein interaction network-guided cellular engineering

Gerd Moe-Behrens's insight:

*Opportunities for protein interaction network-guided cellular engineering*  

by
Phillip C. Wright, Stephen Jaffe, Josselin Noirel, Xin Zou

"As we move further into the postgenomics age where the mountain of systems biology-generated data keeps growing, as does the number of genomes that have been sequenced, we have the exciting opportunity to understand more deeply the biology of important systems, those that are amenable to genetic manipulation and metabolic engineering. This is, of course, if we can make ‘head or tail’ of what we have measured and use this for robust predictions. The use of modern mass spectrometry tools has greatly facilitated our understanding of which proteins are present in a particular phenotype, their relative and absolute abundances and their state of modifications. Coupled with modern bioinformatics and systems biology modelling tools, this has the opportunity of not just providing information and understanding but also to provide targets for engineering and suggest new genetic/metabolic designs. Cellular engineering, whether it be via metabolic engineering, synthetic biology or a combination of both approaches, offers exciting potential for biotechnological exploitation in fields as diverse as medicine and energy as well as fine and bulk chemicals production. At the heart of such effective designs, proteins' interactions with other proteins or with DNA will become increasingly important. In this work, we examine the work done until now in protein–protein interactions and how this network knowledge can be used to inform ambitious cellular engineering strategies. Some examples demonstrating small molecules/biofuels and biopharmaceuticals applications are presented..."
http://bit.ly/WgLHBH

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January 3, 2013 2:22 PM
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2012: Signaling Breakthroughs of the Year

Gerd Moe-Behrens's insight:

by
Michael B. Yaffe and Nancy R. Gough

"With input from the members of the Board of Reviewing Editors and editorial staff, Science Signaling puts the spotlight on the hottest signaling research of 2012. The connection between signaling and metabolism continues to be an important area. Signaling breakthroughs in cancer, immunology, developmental biology, neuroscience, and microbiology all made the list. Structural and molecular insights into signaling proteins and networks are also beginning to not only yield potential therapeutic targets but also lead to successful efforts between synthetic biologists and clinicians in the treatment of cancer."

http://bit.ly/UqxgwO

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January 2, 2013 4:41 PM
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States of Design 07: Bio-design - Design - Domus

States of Design 07: Bio-design - Design - Domus | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

by Paola Antonelli

"When the materials of design are not plastics, wood, ceramics or glass, but rather living beings or living tissues, the implications of every project reach far beyond the form/function equation and any idea of comfort, modernity or progress. Design transcends its traditional boundaries and its implications aim straight at the heart of the moral sphere, toying with our deepest-seated beliefs. The figure of the mad scientist playing God in order to create a new being that turns into a harbinger of Armageddon does not, however, apply to most bio-designers. Some work with visible organisms such as plants and animals, others with bacteria and cells, others still tinker with DNA to create new beings, but they never work alone in an ethical vacuum, preferring instead teams that also comprise physicists, mathematicians, computer scientists, engineers, chemists and bio-ethicists, and sometimes even economists and philosophers. Their work is encouraged and celebrated in a few centres of "irradiation" of these new ideas, such as the indomitable Design Interactions programme at the Royal College of Art in London, the Science Gallery at Trinity College in Dublin, and the Paris-based Le Laboratoire gallery and research centre founded in 2007 by David Edwards, a professor of Biomedical Engineering at Harvard, which has helped designer Mathieu Lehanneur propel himself in this realm. Many of them were featured in MoMA's 2008 exhibition Design and the Elastic Mind and are now part of the museum's collection..."

 http://bit.ly/vpMIOC

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January 1, 2013 12:39 PM
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Are We Becoming Cyborgs?

Are We Becoming Cyborgs? | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:

CONVERSATION
Serge Schmemann
Susan Greenfield
Maria Popova

"SINCE broadband began its inexorable spread at the start of this millenium, Internet use has expanded at a cosmic rate. Last year, the number of Internet users topped 2.4 billion — more than a third of all humans on the planet. The time spent on the screen was 16 hours per week globally — double that in high-use countries, and much of that on social media. We have changed how we interact. Are we also changing what we are?

We put that question to three people who have written extensively on the subject, and brought them together to discuss it with Serge Schmemann, the editor of this magazine. The participants: Susan Greenfield, professor of synaptic pharmacology at Oxford. She has written and spoken widely on the impact of new technology on users’ brains. Maria Popova, the curator behind Brain Pickings, a Web site of “eclectic interestingness.” She is also an M.I.T. Futures of Entertainment Fellow and writes for Wired and The Atlantic. Evgeny Morozov, the author of The Net Delusion: The Dark Side of Internet Freedom . He is a contributing editor to The New Republic ...."

http://nyti.ms/VXOz63

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December 30, 2012 1:37 PM
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Sage Bionetworks

Sage Bionetworks | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:


"Understanding human biology requires a new community-based vision of open access innovation that respects and links all stakeholders and supports a new culture of cooperative, data-intensive science.

We pledge to take up this challenge and have drafted the Sage Bionetworks Commons Principles to guide the development of an open source community where computational biologists can develop and test competing models built from common resources.  These principles will guide the operations and evolution of the Commons, through its policies, procedures and practices.  The Principles will be revised and refined as experience accumulates with initial governance of the Commons guided by two Sage Bionetworks Directors and two external experts."
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December 30, 2012 12:18 PM
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Systems Biology 305qc: Practical Synthetic Biology « Systems Biology – HMS

Systems Biology 305qc: Practical Synthetic Biology « Systems Biology – HMS | SynBioFromLeukipposInstitute | Scoop.it
Gerd Moe-Behrens's insight:
Instructors:Pamela A. Silver, Jeffrey Way, & Stephanie Hays (Teaching Fellow) "Synthetic biology is a new discipline that seeks to enable the predictable engineering of biological systems. According to one conception of synthetic biology, proteins and genetic regulatory elements are modular and can be combined in a predictable manner. In practice however, assembled genetic devices do not function as expected. The purpose of the course is to go beyond the textbook, first-pass description of molecular mechanisms and focus on details that are specifically relevant to engineering biological systems." http://bit.ly/UCeMvh
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