Mostrando entradas con la etiqueta Genómica Sintética. Mostrar todas las entradas
Mostrando entradas con la etiqueta Genómica Sintética. Mostrar todas las entradas

jueves, 25 de septiembre de 2014

DNA: The Software of Life


J. Craig Venter

BIO
J. Craig Venter, Ph.D., is a biologist renowned for his contributions in sequencing the first draft human genome in 2001, the first complete diploid human genome in 2007 and construction of the first synthetic bacterial cell in 2010. He is founder, chairman and CEO of the J. Craig Venter Institute (JCVI). He is also a co-founder and CEO of Synthetic Genomics Inc (SGI), a privately held company focused on developing products and solutions using synthetic genomic technologies; and a co-founder and CEO of Human Longevity Inc (HLI), a privately held genomics and cell therapy-based diagnostic and therapeutic company focused on extending the healthy, high performance human life span. He and his teams are focused on a variety of projects and programs including: 
  • synthetic genomic research and the application of these advances to develop new vaccines and food and nutritional products, new biofuels and biochemicals; 
  • continued analysis of the human genome including the human microbiome, and discovering and understanding genetic diversity in the world's oceans. 
Dr. Venter is a recipient of the 2008 National Medal of Science and is a member of the National Academy of Sciences. He is the author of "Life at the Speed of Light: From the Double Helix to the Dawn of Digital Life" (Viking, 2013) and "A Life Decoded: My Genome: My Life" (Viking, 2007).


ORIGINAL: Zeitgeist Minds

domingo, 6 de enero de 2013

Going below 0K, genomic editing, molecular motors, mechanochemistry, cellular reprogramming, and others.

ORIGINAL: SciTechDigest
SciTech #ScienceSunday Digest 1 - 
6th Jan 2013

1. Conceptualising Negative “Absolute” Temperatures.
Physicists have used finely controlled magnetic fields and lasers to force the temperature of a gas to be colder than absolute zero, i.e.minus a few billionths of a degree below zero Kelvinhttp://phys.org/news/2013-01-gas-temperature-absolute.html andhttp://www.nature.com/news/quantum-gas-goes-below-absolute-zero-1.12146. This is of course intriguing, but depends crucially on the definition of temperature and entropy. The matter itself is apparently not at temperatures below zero Kelvin but rather on average the system as a whole exhibits an average temperature that can be measured as below zero - this actually depends on heating the particles up while driving their entropy down. Negative temperatures imply negative pressures and so this naturally leads to stimulating speculation on how this finding might be applied to things like dark energy, new forms of matter, repulsive gravity and mass, warping space, wormholes, and Alcubierre drives. h/t +Ninja On Rye

2. More Precise Genomic Editing.
By modifying a set of bacterial proteins that normally defend against viral invaders researchers created a system that can alter several genome sites simultaneously and can achieve much greater control over where new genes are insertedhttp://web.mit.edu/newsoffice/2013/editing-the-genome-with-high-precision-0103.html. This approach can be used to disrupt a gene or replace it with a new one; the specific sequence of the RNA component allows the easy programming of a nuclease to target one or more positions in the genome. The genetic components have been deposited with a nonprofit to be made widely available to other researchers via http://crispr.genome-engineering.org/ and so we now have a cheaper, easier-to-use, more precise and accurate, widely available system that can be used to engineer a wide range of organisms for countless biotechnology and synthetic biology applications. I’ve gotten the occasional cold sore since I was a child and so would love something like this to target the HSV code buried in some cells. 

3. A Molecular Motor Rotating on an Atomic Ball Bearing.
Title says it all. Some very clever chemists created two complex individual molecules (i) a base with three legs joined to a boron and ruthenium atom, and (ii) a top with five arms joined to a five atom ring in the centre http://arstechnica.com/science/2012/12/single-molecule-motor-sits-on-a-single-atom-ball-bearing/ (image 2). When the 5-armed molecule was placed on the ruthenium atom a scanning tunnelling microscope was used to inject electrons into the system and controllably cause the top molecule to rotate clockwise and anticlockwise. I’m wondering whether this little molecular motor might be used as a switch (it can be moved in one-arm increments) in some form of ultra-dense mechanical computer memory or processing element? h/t +iPan Baal


4. On Progress to Superhuman Immune Systems.
In a type of study that is becoming increasingly common, researchers took mature immune cells from a patient, treated them with a known cocktail of factors to turn them into induced pluripotent stem cells, replicated / expanded the population of cells, and turned them back into the same type of cell but these new cells exhibited rejuvenated characteristics of lifespan and growth potential while retaining the ability to target cancer cells and HIV-infected cellshttp://www.fightaging.org/archives/2013/01/why-not-infuse-a-person-with-many-many-many-immune-cells.php. Reason from FightAging! posits that it is surely only a matter of time before we safely imbue a person with rejuvenated populations of 2, 5, or even 10 times as many immune cells as we normally have. 

5. A Topological Recipe Book for New Materials.
Researchers showed that they can create a recipe book to build new materials using the mathematics of topology (whose properties that do not change when an object is continuously deformed)http://www.colorado.edu/news/features/physicists-research-creates-recipe-book-new-materials (image 1). They created a colloid by injecting tiny differently-shaped particles (that represent fundamental building-block shapes in topology) into a liquid crystal to create a novel substance that behaves somewhat like a liquid and somewhat like a solid. The new material adhered to existing mathematical topology theorems and should open the door to a range of new materials in this space. 


6. Uncovering Drug Side Effects Before Drug Trials.
A research group has created a computational / simulation tool that rapidly screens drug structures against a library of known protein structures in order to identify likely unwanted interactions and deleterious side-effects http://phys.org/news/2013-01-method-uncovering-side-effects-drug.html. The proof-of-concept correctly predicted 969 side-effects of 658 drugs that are in widespread medical use, and also identified possible side effects for many uncharacterized experimental molecules. The new method could be helpful in uncovering serious side effects early in the development and testing of new drugs and so avoid costly investment in trials and marketing, ideally leading to cheaper medications and a quicker and improved regulatory process. 

7. Smart Drug Design Reverses Alzheimer’s Symptoms and Restores Memory Loss.
A new drug candidate derived from the regulator of a key brain enzyme called Cdk5 - overactivation of which is implicated in plaque formation - was shown to restore memory loss and reverse symptoms of Alzheimer’s disease in mice (engineered to develop the disease) when injected http://www.eurekalert.org/pub_releases/2013-01/foas-pcr010213.php. The mice experienced no signs of side-effects and the group is planning to conduct human trials with the hope of demonstrating the same effect in humans. The more we understand biology, the greater mechanistic insight we uncover into the workings of various molecular pathways and the structure of the molecules involved the more advances like this will be uncovered and developed: rationally designed molecular mimics or segments of natural molecules designed to plug and interfere with diseased proteins and enzymes. 

8. Mechanochemistry and Molecular Levers.
Researchers exploring stress-responsive materials discovered a particular molecular backbone that can act like a lever to open a molecular ring embedded within it when microscopic tweezers are used to grab onto two parts of the atomic chains and pull them so that they break open and react in certain spots http://phys.org/news/2012-12-molecular-levers-materials.html. In some cases these mechanically-induced chemical reactions occurred orders of magnitude faster than predicted. Advances like this obviously bring to mind Drexler’s nanomachanical chemical fabricators - a billion pushes and pulls per second producing a billion new molecular products. 

9. Instructing Scar Tissue to Change Itself into Healthy Tissue.
By using a cocktail of three specific genes researchers have used gene therapy to reprogram the scar tissue cells on a damaged heart into functional muscle cells, while the addition of a fourth gene stimulated the growth of blood vessels to enhance the effect 
http://www.fightaging.org/archives/2013/01/instructing-scar-tissue-to-change-itself-into-healthy-tissue.php. So here we have a specific gene therapy, targeted to a specific population of cells (heart scar tissue) and turning these cells into more useful cells in order to repair an organ (the heart) and attain a close-to-normal healthy functioning organ. No cells, no drugs, just injected remote cellular reprogramming. 

10. Nanowire Arrays for Better Piezoelectric Energy Generators.
Researchers developed a nanogenerator consisting of an array of vertically aligned nanowires that, when deformed by an impact or twist induces a piezoelectric production of electronshttp://phys.org/news/2013-01-nanogenerator-output-triples-previous.html. The proof-of-concept work included producing enough energy to turn on an LED light, and the much more interesting case of the flick of a finger being enough to activate the nerves of a frog’s leg and cause a kick - the embedded video in the linked page is worth a watch. 

An archive of 2012 SciTech Digests can be found here: http://www.scitechdigest.net/

lunes, 7 de mayo de 2012

Synthetic Biological Life

ORIGINAL: HPlusMagazine
By: Laura E. Bratton, MD, Rodney Shackelford, DO, Ph.D.
May 3, 2012

The idea of producing artificial or synthetic life has long fascinated mankind and from ancient times many human and animal-imitating “automata” or self-operating machines have been created for entertainment, instructional, and sometimes religious purposes. The creation of actual synthetic biological life only became possible with the discovery of the structure of DNA, the genetic code, and the development of the basic tools of molecular biology, such as the ability to isolate, sequence, and join different DNA sequences. Especially important has been the recently developed ability to artificially synthesize relatively long DNA molecules with designed sequences. Although the creation of completely synthetic biological life was first accomplished in 2010, the field is already yielding significant information concerning the core gene groups or genetic “chassis” indispensible for life and how these gene products (proteins, RNAs, and lipids) function as an integrated unit. With the identification of these chassis, exogenous natural or synthetic gene sequences can be integrated into organisms designed for specific purposes and applications.

The first genetically engineered organism was created in 1973 when a naturally occurring DNA sequence was transferred into and expressed in a bacterium, conferring antibiotic resistance. The first organism to actually have a synthetic (or man-made “added”) biochemical pathway was created in 2003, when an E. coli was artificially created with a new genetic code and amino acid synthesizing enzymes. The engineered bacterium could synthesize and incorporate an amino acid (O-methyl-L-tyrosine) that does not normally occur in nature into proteins, increasing the number of amino acids used in virtually all life forms from twenty to twenty-one amino acids. Thus a new, human-designed functioning genetic chassis and genetic code was placed into a microorganism.

In 2010, after some fifteen years of intense research effort, the first entirely synthetic organism was created with a genome entirely synthesized “out of four bottles” i.e., chemically synthesized from the four DNA bases; thymine, cytosine, guanine, and adenine. The organism was partially based on M. mycoides, a genetically simple microorganism containing roughly 480 protein-encoding genes and a genome size of 1.08 million DNA base pairs – in comparison the human genome has roughly 20,500 genes over three billion DNA base pairs. The synthetic genome was chemically synthesized in 80-90 base units and slowly assembled into “DNA cassettes”, verified by sequencing, and assembled into a circular genome. To insure that no natural DNA contaminated the synthetic DNA “watermark” sequences were inserted into synthetic genome to differentiate it from the natural M. mycoides genome. Additionally, antibiotic resistance genes were added and a disease-inducing gene was removed from the synthetic genome. The resulting genome was place in an empty M. capricolum cell (i.e., without a nucleus) and the resulting synthetic life from was able to grow in culture indefinitely. Since 2010 this synthetic organism has been useful in identifying the “minimal genome” required for life – about 380 of the 480 protein-encoding genes. Additionally, comparison of the synthetic organism to similar naturally occurring organisms (Mycoplasmas), allowed the identification of gene groups involved in cellular processes such as 
  • information storage, 
  • metabolism, 
  • energy production and conversion, and 
  • cell membrane biogenesis. 
Identification of these gene sets is an important first step designing synthetic life that can perform specific functions.

Although a significant first step in the creation of synthetic biological life, this initial work met with extensive criticism. The researchers who made synthetic life were accused of “playing God” and possibly opening up a new technology that would allow the creation of “biological super weapons”. The later objection has some validity, as existing DNA synthesis and end-joining technology could allow the synthesis of fully infective polio or smallpox viruses. Other researchers pointed out that the new synthetic organism was a nearly one-to-one copy of a naturally occurring organism and for it to grow the synthetic genome had to be placed into a naturally occurring Mycoplasma that had its nucleus removed. Thus, other than the DNA being artificially synthesized, there was relatively little that was actually new about the organism. The creators of the new organism pointed out that this is a first step of many and “creating life from scratch” will come later.

Currently the immediate focus in synthetic biological life research is to use simple synthetic organisms to define the “minimal genome”, or the smallest set of genes required to support life and identify the components and functions of “biological gene-chassis” and find ways to modify these chassis. Specific applications include the creation of synthetic organisms that can: 
  1. efficiently produce pharmaceuticals and vaccines that are otherwise difficult and expensive to produce, 
  2. efficiently produce hydrocarbon biofuels (replacing oil, coal, etc.), and 
  3. be useful as plant feedstock in agriculture, lowering the need for increasingly expensive petroleum-based fertilizers. 
An example of such an application has been inserting the enzymes for artemisinic acid synthesis into baker’s yeast. Artemisinic acid is the chemical precursor anti-malarial drug artmisinin, a drug that is currently extracted from the sweet wormwood plant at high cost, reducing the drugs availability in poorer countries. Once the enzymatic pathway is in place and efficiently working, the drug could be produced cheaply in large amounts through a process resembling brewing beer. Several of these projects are being researched at Synthetic Genomics, a new biotechnology company specializing in the creation of synthetic life for specific applications.

Not surprisingly the creation of synthetic animal life is more complex and difficult than for simpler microorganisms. However, a round worm (C. elegans) was created that carried an extensively expanded genetic code and protein synthesis pathways, allowing the incorporation of multiple novel (or “unnatural”) amino acids into the animal’s proteins. These protein modifications would facilitate the study of protein localization and interactions within a living animal. Additionally, modified proteins could be designed for specific purposes, such as protein-based drugs with very long half-lives due to novel amino acids that inhibit normal cellular protein degradation.

Although difficult, our present molecular biology technology could allow the creation of more complex organisms, including fungi and even animals. The present challenges in creating synthetic life include the following:
  1. Create synthetic life “from scratch” without the need to largely copy existing life forms.
  2. Improve on our ability to design and integrate molecular pathways within synthetic life.
  3. Create a strategy or “algorithm” to for the efficient creation of synthetic life forms.
  4. Create policies and rules to prevent the creation of synthetic life forms that may be harmful, such as human pathogens (smallpox, virulent influenza viral types, etc.).
With time these goals could be achieved and the technology to accomplish these goals is largely in place.

In the more distant future synthetic biology could allow the extensive modification of existing genomes and even the creation of entirely new genomes and species. While this is the goal of many Transhumanists, one hopes that if and when such technology exists, the human race has the intelligence to apply such technology with wisdom.

Dr. Shackelford is an Assistant Professor of Clinical Pathology at Tulane Medical Center. He has a DO degree from Des Moines University of Osteopathic Medicine and a Ph.D. in molecular pathology from Duke University. His areas of research include DNA repair, molecular mechanisms of carcinogenesis, and cell division.

jueves, 19 de abril de 2012

ADN alternativo creado por científicos

ORIGINAL: TheGuardian
Ian Sample
19 Abril 2012

El material genético artificial - XNAs - se espera que revele cómo las moléculas se replicaron inicialmente y que impulse la investigación en biotecnología

ADN y el ARN se han convertido en alternativas de polímeros genéticos llamados XNAs por los investigadores en Cambridge. Fotografía: Mopic / Alamy
Los científicos han creado el material genético artificial que puede almacenar información y evolucionar a través de generaciones de una manera similar al ADN - una hazaña que espera que de un impulso a la investigación en Medicina y Biotecnología, y arroje luz sobre cómo las moléculas se replicaron inicialmente y se ensamblaron en miles de millones de años de vida.

En última instancia, la creación de alternativas al ADN podría permitir a los científicos para hacer nuevas formas de vida en el laboratorio.

Los investigadores del Laboratorio de Biología Molecular MRC, en Cambridge, desarrollaron procedimientos químicos para activar el ADN y ARN, las bases moleculares de toda la vida conocida, en seis polímeros alternativos genéticos llamados XNAs.

El proceso intercambia la desoxirribosa y ribosa (la "d" y "r" en el ADN y el ARN) por otras moléculas. Se encontró los XNAs podría formar una doble hélice con el ADN y eran más estables que el material genético natural.

En la revista Science, los investigadores describen la forma en que lograron que una de las XNAs se adheriese a una proteína, una habilidad que puede significar los polímeros podría implementarse como drogas trabajando como los anticuerpos.

Philipp Holliger, autor principal del estudio, dijo que el trabajo demostró que dos sellos distintivos de la vida, la herencia y la evolución - era posibles usando alternativas al material genético natural.

"No hay nada de esecialidad ("Goldilocks") en el ADN y el ARN", dijo Holliger a Science. "No hay ningún imperativo abrumador o funcional para que los sistemas genéticos o la biología se basen en estos dos ácidos nucleicos".

Vitor Pinheiro, un co-autor del artículo, dijo que la investigación podría ayudar a los científicos no elegir cómo el ADN y el ARN se hizo tan crucial en la evolución de la vida, y tal vez incluso ayudar en la búsqueda de organismos extraterrestres. "Si un sistema genético no tiene que estar basado en ADN y ARN, ¿Entonces cómo vas a  definir la vida? ¿Cómo buscarías vida?" dijo.

En un artículo adjunto, Gerald Joyce, del Instituto de Investigación Scripps en La Jolla, California, dice que el estudio anuncia una "era de la genómica sintética, con implicaciones para la exobiología [que se ocupa de la vida extraterrestre] vida, la biotecnología y la comprensión de sí mismo". Y añade: "La construcción de los sistemas genéticos basados en plataformas de productos químicos alternativos en última instancia, puede conducir a la síntesis de nuevas formas de vida".

Otros científicos, entre ellos un equipo de la J Craig Venter Institute, en Rockville, Maryland, están esperando para hacer organismos sintéticos desde cero, pero la mayoría de los trabajos hasta el momento ha utilizado el ADN convencional.

En su artículo sobre el estudio de Cambridge, Joyce alude a los peligros potenciales de la genómica sintética. Él escribe: "A medida que uno contempla todas las formas de vida alternativas que podrían ser posibles con XNAs y otras moléculas genéticas más exóticas, las palabras de Arthur C. Clarke, vienen a la mente En "Año 2010: Odisea dos", HAL del equipo le dice a la humanidad,
" todos estos mundos son suyos ", pero advierte -.., intenta desembarcar en ellos excepto en Europa (la luna de Júpiter)".
Hay biólogos están empezando a retozar en los mundos alternativos de la genética, pero no se debe andar en áreas que tienen el potencial de dañar nuestra biología."