Difference between revisions of "Technology level 0"

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= Overview  =
 
= Overview  =
  
At the current technology level we have a '''top-down - bottom-up - technology-gap''' which is about to close.  
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At the current technology level we have a '''top-down bottom-up technology-gap''' which is about to close.  
  
At the top-down side we have:  
+
Bottom-up with self assembly:
  
*MEMS technology (e.g. grippers, MEMS AFM)  
+
*structural 3D DNA nanotechnology<ref>"Cryo-EM structure of a 3D DNA-origami object" Xiao-chen Bai, Thomas G. Martin, Sjors H. W. Scheres, Hendrik Dietz</ref> [http://www.pnas.org/content/109/49/20012.full] & Co (self assembling structures) [https://en.wikipedia.org/wiki/DNA_origami]
*microelectronics (e.g. for electrostatic actuation)<br>  
+
*foldamers designed for predictable folding (e.g. synthetic proteins)<br>
*AFM arrays (cruder then singe tip AFMs)  
+
*polyoxymetalates (POMs)
*other [add if you know relevant ones]<br>
+
*other [add if you know relevant ones]
  
At the bottom-up side we have:  
+
Bottom-up with mechanosynthesis and self assembly:
  
*structural 3D DNA nanotechnology<ref>"Cryo-EM structure of a 3D DNA-origami object" Xiao-chen Bai, Thomas G. Martin, Sjors H. W. Scheres, Hendrik Dietz</ref> [http://www.pnas.org/content/109/49/20012.full] & Co (self assembling structures) [https://en.wikipedia.org/wiki/DNA_origami] <br>
+
*patterned layer epitaxy with scanning tunneling microscopes (STM)
*foldamers designed for predictable folding (e.g. synthetic proteins)<br>
+
*polyoxymetalates (POMs) <br>
+
*patterned layer epitaxy with scanning tunneling microscopes (STM)<br>
+
 
*other [add if you know relevant ones]
 
*other [add if you know relevant ones]
 +
 +
Top-down side:
 +
 +
*MEMS technology (e.g. grippers, MEMS AFM)
 +
*microelectronics (e.g. for electrostatic actuation)
 +
*AFM arrays (cruder then singe tip AFMs)
 +
*other [add if you know relevant ones]
 +
  
 
[TODO clarify the problems]  
 
[TODO clarify the problems]  
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== Capabilities, Limits and Unknowns  ==
 
== Capabilities, Limits and Unknowns  ==
  
Mechanical and micromechanical systems such as AFMs and MEMS are generally very slow to slow. ['''TODO''' add quantitative numbers]<br>beside the problem of yet unstable tooltips It seems certain that they are to slow to do atom by atom assambly.<br>'''To investigate:''' Will they be fast enough to do e.g. 3DDNA-block by 3DDNA-block assembly?  
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Mechanical and micromechanical systems such as AFMs and MEMS are generally very slow to slow. ['''TODO''' add quantitative numbers]<br>beside the problem of yet unstable tooltips and unsufficient vacuum It seems certain that they are to slow to do direct [[mechanosynthesis]].<br>'''To investigate:''' Will they be fast enough to do e.g. assembly of 3DDNA-blocks?  
  
Electric fields generated by microelectronics acting on a 3DDNA or an other type of block-structure in ''machine phase'' provide less degrees of freedome than a mechanical gripper. More problematically the blocks need to be made dielectric or charged to be effected by the field.<br>'''To investigate:''' Can blocks/block structures be made dielectric or charged?  
+
Electric fields generated by microelectronics acting on a DNA brick structure or an other type of structure in ''machine phase'' provide less degrees of freedome than a mechanical gripper. More problematically the blocks need to be made dielectric or charged to be effected by the field.<br>'''To investigate:''' Can blocks/block structures be made dielectric or charged sufficiently?  
  
The size of the smallest possible MEMS grippers and 3DDNA-blocks aren't overlapping yet ['''TODO''' add size comparison], that is the tip radius of the grippers tend to be reater than dte 3DDNA block sizes. So they need to be aggregated to even bigger sizes to be grippable.<br>'''To inverstiate:'''<br>  
+
The size of the smallest possible MEMS grippers and DNA-bricks aren't overlapping yet ['''TODO''' add size comparison], that is the tip radius of the grippers tend to be greater than the DNA-brick sizes. So they need to be aggregated to even bigger sizes to be grippable.<br>'''To inverstiate:'''<br>  
  
 
*Can 3DDNA-blocks be hirachically self assembled, that is can the blocks surfaces be glued together by adding strands in a second step?  
 
*Can 3DDNA-blocks be hirachically self assembled, that is can the blocks surfaces be glued together by adding strands in a second step?  
*Alternatively do complementary surfaces stick by VdW interaction even though the strands doesn't match?<br>
+
*Alternatively do complementary surfaces stick by VdW interaction even though there are no open strands (or the strands doesn't match)?<br>
  
 
To be usable for somewhat functional robotic applications the blocks need to fulfill some criteria:<br>'''To investigate:'''  
 
To be usable for somewhat functional robotic applications the blocks need to fulfill some criteria:<br>'''To investigate:'''  

Revision as of 10:59, 14 December 2013

Overview

At the current technology level we have a top-down bottom-up technology-gap which is about to close.

Bottom-up with self assembly:

  • structural 3D DNA nanotechnology[1] [1] & Co (self assembling structures) [2]
  • foldamers designed for predictable folding (e.g. synthetic proteins)
  • polyoxymetalates (POMs)
  • other [add if you know relevant ones]

Bottom-up with mechanosynthesis and self assembly:

  • patterned layer epitaxy with scanning tunneling microscopes (STM)
  • other [add if you know relevant ones]

Top-down side:

  • MEMS technology (e.g. grippers, MEMS AFM)
  • microelectronics (e.g. for electrostatic actuation)
  • AFM arrays (cruder then singe tip AFMs)
  • other [add if you know relevant ones]


[TODO clarify the problems]

Capabilities, Limits and Unknowns

Mechanical and micromechanical systems such as AFMs and MEMS are generally very slow to slow. [TODO add quantitative numbers]
beside the problem of yet unstable tooltips and unsufficient vacuum It seems certain that they are to slow to do direct mechanosynthesis.
To investigate: Will they be fast enough to do e.g. assembly of 3DDNA-blocks?

Electric fields generated by microelectronics acting on a DNA brick structure or an other type of structure in machine phase provide less degrees of freedome than a mechanical gripper. More problematically the blocks need to be made dielectric or charged to be effected by the field.
To investigate: Can blocks/block structures be made dielectric or charged sufficiently?

The size of the smallest possible MEMS grippers and DNA-bricks aren't overlapping yet [TODO add size comparison], that is the tip radius of the grippers tend to be greater than the DNA-brick sizes. So they need to be aggregated to even bigger sizes to be grippable.
To inverstiate:

  • Can 3DDNA-blocks be hirachically self assembled, that is can the blocks surfaces be glued together by adding strands in a second step?
  • Alternatively do complementary surfaces stick by VdW interaction even though there are no open strands (or the strands doesn't match)?

To be usable for somewhat functional robotic applications the blocks need to fulfill some criteria:
To investigate:

  • Can an axle bearing system be built that runs non self distructively wit sub blocksize precesicion?
  • Can the blocks bind strong enough together to avoid falling apart when actuated?
  • Are the surfaces of 3DDNA blocks made with half strands, that is are there surfaces smooth ore more like a hairy ball) [TODO dig out the known answer]
  • Can two blocks be connected with a edge to edge hinge? (similar to the hirachical assembly question)

To use electric fields as input the block structures need to provide at least one internal 1D degree of freedome which can be compressed to 0D (machine phase)
To investigate: How to create minimal sized block structures for mechanical or electrostatical acutation that are productive and capable of self replication?

Proposals for the step from T.Level 0 to 1

[TODO to myself: add the one I've archived] technology level I


Some raw notes about ideas to block based anosystems:

  • (enclosed) Serving plates
  • exoergic chain & alternatives?
  • "look" and pick
  • tooltip size adapter - spanning up down gap
  • block reloading
  • electrostatic actuation & signal collector bundles & broadcasting
  • bulldozing
  • pros of dry operation
  • parallel robots -> less complex mechanics
  • linkages
  • temporary pinning
  • rotation vs reciprocation
  • replicative: build volume limit -> 2D mobility
  • parallel: accuracy issue - effort in parallelisation of tips leaves them too unprecise ...

Investigation Results

Space for investiganion results and further investigation-directions:

[yet empty]


Modular Molecular Composite Nanosystems (MMCS)

[...] Links:

Structural DNA nanotechnology

[...] When one watches the simulation of the self assembly process of DNA bricks [TODO add link] one is led to doubt the stiffness of the product. The DNA double helix can create siff polymeres if the used doublehelix segments are kept in the length range from one to three turns. Mentioned here [3] under the section "DNA as Construction Material" and referenced here [2] (unchecked). Is there quantitative information about the stiffnes of whole DNA bricks (to investigate)?

Medicine

The exclusive interest in medical devices of T.Level 0 motivated by near term benefits drives development now.
With rising technology levels we want to get further and further away from biological nanosystems though.
Therefore a situationmay where no dedicatet non medical research is done might let us be stuck for a quite longr time than necessary.

References

  1. "Cryo-EM structure of a 3D DNA-origami object" Xiao-chen Bai, Thomas G. Martin, Sjors H. W. Scheres, Hendrik Dietz
  2. Hagerman, P.J. (1988), Flexibility of DNA, Ann. Rev. Biophys. & Biophys. Chem. 17, 265-286.

DNA screw