It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
originally posted by: cooperton
originally posted by: peter vlar
In "The Origin Of Species" (1859), Darwin said:
"If it could be proved that any part of the structure of any one species had been formed for the exclusive good of another species, it would annihilate my theory, for such could not have been produced through natural selection."
You're avoiding the issue of irreducible complexity. Darwin also said this:
Incremental mutations cannot suffice the multi-faceted aspects of, for example, the development of a functional muscle unit.
All these aspects are required for functional skeletal muscle. Adding a new protein to it is not as easy as miraculously mutating a new useful protein (never been witnessed in a lab), because it also has to be directed to the relevant location in the body and synchronize with the rest of the muscle units. Again, never observed in a lab. Mechanistically, it is unthinkable for such an event to occur
As darwin said, if it were to be found that any organ (or any functional component of the body for that matter) could not have formed by successive mutations, the theory becomes invalid. Skeletal Muscle, among many other examples, could not have formed by successive mutations because of the multiple types of proteins involved, and also the proper assemblage of these pieces. Therefore Darwin is right, the theory is invalid as demonstrated by biological science.
Cross-bridges on self-assembled smooth muscle myosin filaments☆
Author links open overlay panelApolinarySobieszek Show more doi.org...(72)90573-6Get rights and content
Abstract
A crude myosin fraction may be obtained from vertebrate smooth muscle under low ionic-strength conditions, in which a self-assembly of filaments varying from 0.3 to 1.5 μm in length is seen to take place. These filaments show a constant repeat of about 140 Å, which arises from a regular helical arrangement of projections or cross-bridges. The repeat may be followed along the entire length of the filaments, that is, there is no bare zone. The mode of assembly of these filaments is discussed.
originally posted by: puzzlesphere
Oh... and you saying "this is too complex" without showing why
You just can't get past the Appeal to Complexity can you?
Do you understand? Or are you just going to do an appeal to complexity and say I'm wrong because you can't comprehend the biological concepts I am addressing?
originally posted by: Phantom423
Now, what was it you were going to say about myosin filaments and self assembly?? Gee, someone already did that!
originally posted by: Phantom423
a reply to: cooperton
So post the article. Let's see how it was done.
originally posted by: Phantom423
What's wrong with self assembly experiments? What's wrong with the myosin filament experiment?
originally posted by: cooperton
originally posted by: Phantom423
What's wrong with self assembly experiments? What's wrong with the myosin filament experiment?
Explain the self-assembly mechanism of myosin. You posted the paper. explain how it works and we will go from there.
originally posted by: Phantom423
a reply to: cooperton
You want to remain in perpetual ignorance, that's your business. You're a lousy salesman because I doubt you've brought anyone on this board, or anywhere else for that matter, to your side.
The evidence is self evident. Do you have evidence? NO.
Hundreds of experiments and research papers have been published on this topic. Do you have any experiments or research papers? NO.
Have you ever performed ANY experiment in a lab? NO.
Do you know anyone who has performed a credible experiment in a legitimate lab? NO.
You're done.