http://groups.google.com/group/the-vegas-group/browse_thread/thread/941d413a6fd5e22b/3389a4601ed87785
Ah, the ever polite folk of the internet, so ready to leap into civilized
discourse. Fortunately, the world isn't bounded in its possibilities by your
horizons, and Reason is in fact my real name.
> Why not apply for an OpenWetWare account and help contribute to it?
I think that a distinct initiative to try the production of documentation my
way is a much better option than contributing to that project, especially
given the fairly narrow focus of the Vegas Group on longevity-related
biotech.
> In what way do you intend to turn this into profit - page hits,
> subscription, etc - and if this is to be a community where you are
> crowd-sourcing most or all of the contributions how can you possibly
> think it is morally acceptable to turn a profit?
You pay freelance writers because it is next to impossible to obtain
reliably good work from distributed unpaid volunteers over a project of any
significant length. The Vegas Group isn't intended to make money, nor do I
see it generating revenue; it is intended to do exactly what it says on the
label: build documentation, build relationships, spur meaningful change.
Even if the Vegas Group did generate revenue, there would be nothing wrong
with doing so on the basis of paid labor - and it is certainly the case that
distinct for-profit entities doing something similar might arise to service
other areas of DIYbio-focused biotech documentation that I have no personal
interest in ... but that isn't on the table for me for now. I should close
this line of thought by pointing out that hostility towards profit is not
exactly a sensible attitude when it comes to the growth of any sort of
ongoing, long term ecosystem of relationships and endeavors, this one
included.
Reason
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On the subject of animal testing I saw no reference to that in the text that Bryan posted though I've not looked through the site in more detail. Have I missed something?
1) I want to create documentation for a set of life science / biotech
procedures relating to longevity, and ensure it is freely and widely
available for use. The explanation for why I want to do this is in the
longer material that Bryan posted.
2) The project to start work on this launched a couple of weeks ago, and is
presently gathering interested volunteers.
3) Some of the resulting documentation will be useful to the wider DIYbio
community: supporting procedures, common techniques.
4) Many of the members of this group have knowledge that might be useful in
producing this documentation. So it can't hurt to ask.
5) If you see value in this project, please do volunteer. We need additional
life-science folk at this stage to help break down procedures into lists of
topics and activities suitable for handing out to writers.
6) My experience tells me that you can't produce good results on the back of
freelance, online, distributed writing without paying people. Therefore I
will be putting up money to pay people. This goal is important to me.
It really is that simple. I am frankly surprised to be greeted with such
outright hostility.
Reason
I for one have no objection to anonymity online so long as money isn't involved. I think it's both normal and prudent to keep your identity online secret until it's foolish to continue doing so.
Of course, given that money might be involved, perhaps that allowance doesn't apply.
Also, although I would generally be against attacking people for soliciting collaboration on something, the spam-ring accusation is a bit suspect.
Also, if someone's actually suggesting animal testing as a DIYbio thing, I'd suggest not doing so or encouraging others to do so. Nothing good lies that way: if you want to do animal testing, go get licensed or work in an established facility.
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On 27 Apr 2011 15:51, "J. S. John" <phill...@gmail.com> wrote:
On Wed, Apr 27, 2011 at 10:33 AM, CoryG <co...@geesaman.com> wrote:
>> It really is that simple. I am...
We're very skeptical around here since there were instances of people
pedalling things without much references, names, goals, etc. I don't
understand why you're anonymous if you're running an organization.
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To po...
Also, although I would generally be against attacking people for soliciting collaboration on something, the spam-ring accusation is a bit suspect.
the domain was itself last changed ownership in February
I agree, I think you came on a little quick here CoryG... I would have
offered constructive criticism first, then if things kept sounding
unrealistic, I would have brought out the more severe criticisms. That
said, maybe you know what he's talking about quite well, enough to
skip to the harsh criticisms.
If I was faced with a life threatening or really debilitating disease,
I would certainly be pressed to weigh the options had.... but I might
not be opposed to self-treating (injecting myself with the mouse cure)
depending on my options. It sucks that in the U.S. we don't have those
options in the hospital.... but I really don't know the whole story
with the ins and outs of regulation, and I hope there is a logical
reason behind not having this option.
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Nathan McCorkle
Rochester Institute of Technology
College of Science, Biotechnology/Bioinformatics
My own take on animal experimentation is that the only thing worse than it
is its absence. I look forward to the foreseeable future in which
experiments in silico become cheap enough to naturally displace the vast
majority of in vivo work, and loathe the fact that our human condition
pushes us toward the unpleasant utilitarian decision to conduct animal
studies.
That said: the measure of a scientist is whether they adhere to the
scientific method, not whether they are formally associated with a major
institution. There is a modest range of people out there who are running and
have run animal experiments that fall within the financial range of a
citizen scientist. For example, the fellow who ran a series of fly life span
experiences back a decade or so ago on the Extropy list, or the fellow
presently engaged through volunteer fundraising from Longecity in order to
test laser ablation of lipofuscin on long-lived breeds of nematode.
And that said: the purpose of the Vegas Group project, the long-term
purpose, is to build a bridge between on one side the work demonstrated in
the laboratory but which will never be developed well under the present US
regulatory regime, and on the other side development communities in
Asia-Pacific regions with more permissive medical regulations (e.g. any of
them at this present time, China included, which is a sad statement to be
able to make). My view of the future is that the DIYbio and surround
communities will play a large role in building this bridge - you are too
small and too few to do so well now, but the future of DIYbio looks very
much like the present of the open source software and open hardware
communities. A lot of people, many passionate causes, a vast number of
semi-professional workers and distributed projects.
It doesn't hurt to be too early to the party.
This bridge building starts with documentation; that's the very first step.
How it proceeds from there to relationship building and the final result of
technologies liberated for development in other parts of the world is up to
the participants. I can't imagine that there will be some mad rush of
citizen scientists slavering over their lab rats as a result of falling
costs or growing documentation from all sources - that's just silly fiction.
Some people will try out some steps of the biotech, some people will only
write or edit, or build relationships, or build equipment. Work will be
done, progress will be made.
> Because, we should all be aware that there are unwary/overly credulous
> readers out there by now.
Which is never a sufficient excuse to hold back from doing one's best to put
out good work and push forward the state of a particular field. Hammers and
knifes have this problem, and every technology since has had it too. The
balance of good is always to forge ahead sensibly.
Reason
That would be step two in the grand bootstrapping, not step one. See my
previous email about the bridge: there are people able to develop over
there, and there are locked-up technologies that are unknown or
underappreciated here. Joining the two is a big grand long-term exercise
that can only really grow in lock-step with the growth of open/DIYbio.
> It is naive to imagine that cures would be used if they existed.
> We have, for example, numerous partial cures for Duchenne's
> muscular dystrophy that have been sitting on the shelf for
> about 6 years while going through the approval process -
> even though you could in some cases just pick up the syringe you
> used on a mouse and apply it to a child and save his life
> (the myostatin gene is identical in humans and mice).
This is exactly the sort of thing that should (a strong word, should, but
that's what I mean) be worked around by any ethical means possible - by
making it more attractive for groups in other regions of the world, beyond
the reach of the FDA and the equivalents in Europe, to pick up this work,
for example. This would be (eventually) through building a process and a
community that can lower their costs of entry, give them a better starting
portfolio of leads to follow, and so forth.
Again, grand visions - but they have to start at the bottom, with validation
of each step. Can you reverse engineer useful techniques from published
papers, can you break it down into sufficiently good documentation that adds
value to the DIYbio community and helps make people more interested, can you
parlay that into connections in Asia and a bigger volunteer community. And
so forth. Each stage, each small step has to add value for someone,
somewhere, who will build on that and help to construct the bridge.
Reason
I would be very interested if you could point me to those numerous people
and any publications showing failure. I'm not talking much to Gencia folk at
the moment because trying to do this without asking for their help is a good
proof of principle. As you point out, there are few published papers, but so
far it looks like that should be enough. See these discussion threads for
the latest:
https://groups.google.com/group/the-vegas-group/browse_thread/thread/4861096
67ad350e1
https://groups.google.com/group/the-vegas-group/browse_thread/thread/2d48c64
4114f8a38
It will not concern me overly if it turns out that protofection can only be
documented to 90% - it is one of many bricks in the bridge and many possibly
early projects. All can be revisited later, and even a partial result can
still lead to a range of good, complete documentation on supporting
procedures, use of equipment, and the like. Or I could go and see if the
Gencia folk are interested in filling in the gaps; it can't hurt to ask.
They are, after all, largely focused at the moment on the mitochondrial
biogenesis aspect of their technology rather than the mitochondrial DNA
transfer - it's their evaluation that the money is in biogenesis, and I'm in
no position to dispute that assessment.
Whether or not protofection comes to a satisfactory conclusion, I have a
possible list of other interesting things for volunteers to work on
documenting, such as work on LysoSENS - which isn't a therapy, but rather a
chance for DIYbio people to actually do some meaningful amateur research.
Synthesize your own lipofuscin components, get some graveyard soil, culture
some bacteria, and see what you come up with. It's a numbers game, but
someone somewhere will find a bug and its enzymes that can break down the
major components of lipofuscin; there's no reason that someone has to be in
an institutional setting.
(As an aside on that topic, I see that the SENS Foundation is presently
hiring a research project lead for LysoSENS work in the Bay Area:
http://www.sens.org/node/2002 - I'm sure there are folk on this list who
would be well suited.)
> Can you post all your protofection references?
These are the two worth looking at:
1) the biogenesis side of the house
http://dx.doi.org/10.1016/j.mito.2010.08.004
2) the 2009 open access paper which makes more sense in the context of the
biogenesis paper above:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829286/
And you can dig up the rest of the older stuff by searching PubMed for
Shaharyar M. Khan, who's the lead. There will probably be a small flood of
publications as and when Gencia sorts out big number funding/a business
relationship/whatever it is they are going to do, but I understand that most
of that is going to be biogenesis-related.
Reason
I'll say this once more and once more only: my real name is Reason. The way
this works offline is as follows:
Rude Person: You're called Reason? Really? Really?
Me: Yes.
Rude Person: Oh.
And that's where it stops. So I'd appreciate it if that's where it stops
here too.
Further, I think it behooves everyone to carefully disentangle whatever
associations they have reflexively built up between (a) the form of a name,
(b) anonymity, and (c) abuse of anonymity. These are three completely
different, separate, and distinct things.
Reason
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My own take on animal experimentation is that the only thing worse than itis its absence. I look forward to the foreseeable future in which
experiments in silico become cheap enough to naturally displace the vast
majority of in vivo work..
"In silico" here meaning to conduct studies using simulations of animals or
animal tissues, as opposed to working in the silicon-based life that seems
so commonplace in our science fiction. The progression of computing power
will make simulated animal models viable fairly soon.
Reason
This statement wrongly assumes that all the interesting pathways have been
fully characterized. This is clearly not true. It doesn't matter how much crunch
you throw at a modeling problem, if your model is incomplete.
--
Russell Whitaker
http://twitter.com/OrthoNormalRuss
http://orthonormalruss.blogspot.com/
No such assumption was made. The pace at which the remaining needed
knowledge is uncovered is itself a function of computing power, and the
present state of the art isn't too shabby. e.g.:
http://news.illinois.edu/news/11/0330cell_ZaidaLuthey-Schulten_ElijahRoberts.html
So fairly soon - by which I meant twenty years. I'm happy to handwave
things over this sort of timescale for fields wherein this is a very large
community of people working on the challenges and established trends in
increased capabilities with no end in sight. This is good enough for me to
base my long-term plans on; your mileage may of course vary.
Reason
> No such assumption was made. The pace at which the remaining needed
> knowledge is uncovered is itself a function of computing power, and the
> present state of the art isn't too shabby. e.g.:
>
> http://news.illinois.edu/news/11/0330cell_ZaidaLuthey-Schulten_ElijahRoberts.html
>
> So fairly soon - by which I meant twenty years. I'm happy to handwave
> things over this sort of timescale for fields wherein this is a very large
> community of people working on the challenges and established trends in
> increased capabilities with no end in sight. This is good enough for me to
> base my long-term plans on; your mileage may of course vary.
>
> Reason
I agree with Cory and Russel on this. You can't model if you don't
know what is actually happening. No amount of computing power could
help you. From my brief experience with comp. chem simulations, my
project and that of the professors in the department all used existing
data. If you don't have data of how the molecules behave, how can I
run experiments. In the same way, for biology, the data must be there
and with the data you can create models, alter parameters and run
in-silico experiments. Computational chemistry/biology will not exist
without the data to run the calculations. And how can you run
calculations without a function. You can't have a modeling function
without understanding how things work.
> -----Original Message-----
> From: diy...@googlegroups.com [mailto:diy...@googlegroups.com] On
> Behalf Of J. S. John
> Sent: Thursday, April 28, 2011 1:55 PM
> To: diy...@googlegroups.com
> Subject: Re: The Vegas Group: bringing quality documentation
> andlongevityscience to DIYbio
>
> I agree with Cory and Russel on this. You can't model if you don't
> know what is actually happening. No amount of computing power could
> help you.
I think I understand where you're going wrong; you're ascribing no value to
simulations that do not reflect reality. Nothing could be further from the
case: simulation/modeling of partially understood complex systems is a
fundamental tool by which those systems can be better understood. That
describes pretty much the entirety of astrophysics, for example.
You can't completely eliminate the need to work with animals and cells: you
need data against which you can to calibrate simulations, for example. But
as the cost of running simulations falls, and the complexity rises, the
utility of using best-present-knowledge simulations to discover new
biochemistry rises. It will displace the bulk of in vivo investigations,
which will remain only to absolutely verify end results. So that's one way
in which things will progress towards ever better simulations, capable of
replacing arbitrary in vivo work.
In terms of obtaining data outside of simulational-deductive methodologies,
is it your believe that twenty years from now, there will not be something
approaching a complete catalogue of pathways for all the most important
areas of mouse and human biochemistry? That would seem unlikely, given
present trends.
Reason
Given that I plan to publish the Vegas Group results as Creative Commons, if
you feel they should be on OpenWetWare, you could always put them there
yourself.
> Not sure why you'd claim that unpaid authors and/or other hosts don't
> create results, when clearly they have and will continue to do so.
Because it is absolutely the case that volunteer projects trying for
specific end goals have a terrible track record. You see the few successes,
but not the innumerable failures. I've been involved in volunteer efforts of
all sorts for more than a decade, and all suffer from the essential problem
that unpaid volunteers have a very high turnover and low productivity. If
you have a specific set of goals in mind and a long term need to keep
volunteers engaged, you can't beat paying people.
Reason
> I agree with Cory and Russel on this. You can't model if you don't
> know what is actually happening. No amount of computing power could
> help you.I think I understand where you're going wrong; you're ascribing no value to
simulations that do not reflect reality. Nothing could be further from the
case: simulation/modeling of partially understood complex systems is a
fundamental tool by which those systems can be better understood. That
describes pretty much the entirety of astrophysics, for example.
Such a procedure as the one that you're interested in, when applied to humans or even mice, will involve many of the sorts of things that are likely to scare the crap out of people, such as a virus-based (or similar) delivery mechanism for direct modification of cells in a living mammalian host.I personally think it's probably not a good idea for the DIYbio movement to get associated with projects like this.
Is this because of the scare factor (a sort of meta phobiophobia), or did something else lead you to that opinion? Just wondering.
I kinda get this feeling too, the last thing we need is the FBI
breaking down our doors and butt-stroking us in the heads over a slime
mold because we're associated with someone touting retrovirus testing
in Humans without FDA approval.
Astrophysics might be a bad example of modelling.. they've had to invent at least three effects for which there is scant-to-no evidence just to preserve the integrity of theory versus model versus reality. Every time I hear about "Dark matter" or "Dark Energy" all I hear is "invisible dragon".
I am somewhere between Reason and the rest. While I know our current models are awful and computation won't immediately solve things, we've only been using the word 'proteome' for two or three decades. Extrapolation of future knowledge based on current rates of research is a bit short sighted, because we don't know what might come around the technological corner.
What if there emerged tomorrow a means to real-time-scan a single cell, down to the macromolecular scale? We'd have the ability to watch everything from protein interactions to transcription to production of stuff like the above mentioned ubiquitination precursors. And with enough computing power, we bould record it, parse it for significant interactions, and probably have a decent model in no time.
It may seem silly to imagine it now but in twenty years we really could have this problem solved and a simulated animal model in the bag.
..although, if your model is faithful enough to reality, is There any difference between cruelty to animals and cruelty to models? :)
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On 29 Apr 2011 04:30, "Gavin Scott" <ga...@allegro.com> wrote:
On Thursday, April 28, 2011 5:06:35 PM UTC-7, Reason wrote:
>
> > I agree with Cory and Russel on th...
Simulations in Astrophysics make sense for things like galaxy formation because the fundamental physics of how particles behave is well understood, and the complexity comes from having effing great numbers of them, not from any lack of information about how they individually behave or interact. As a fluid dynamics problem, we can tell you everything about how one molecule will behave, but can't say much (if anything) about how all of them are going to behave together. There's nothing subtle about simulation at this level. It exposes higher-level aggregate statistical behavior without producing any information on lower-level details.In a cell, the problem is that you don't have the information you need to do a full simulation, and no amount of simulation of the stuff you know will lead to great insights about stuff you don't know. You may discover fascinating aggregate behavior about the stuff you think you already understand, but it will not magically produce anything from a lower (more detailed, closer to reality) level, and where the simulated behavior is affected by the stuff you don't know, the simulation will be wrong (with no hint or a problem until you try to rely on the results and things go all pear-shaped on you).In regard to your proposal, I think the goal of documenting, clarifying, and explaining is a worthy one almost regardless of the subject or the motivation.However, when I read what you're trying to do, I get the feeling that perhaps you're not really interested in mice, but want to make it possible for anyone moderately skilled to be able to follow your procedure to perform an experimental life-extension procedure on themselves or other humans (once a few more details are worked out). You may feel that there is some government conspiracy to withhold the promise of this treatment from the public.
Such a procedure as the one that you're interested in, when applied to humans or even mice, will involve many of the sorts of things that are likely to scare the crap out of people, such as a virus-based (or similar) delivery mechanism for direct modification of cells in a living mammalian host.
I personally think it's probably not a good idea for the DIYbio movement to get associated with projects like this.
I'm sure that further research along the lines you're interested in is going to take place, and as soon as someone comes up with a reproducible reliable, technique that holds the promise of significant benefits to the life extension of humans, then Congress will be pretty quick to nudge the FDA or whoever to change their stance on this (the fact that Congress is mostly comprised of aging white guys is often a benefit to the rest of us :)
G.
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