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(New page: = System Design = ==Domain Level Design== Overall domain level design is illustrated in figure 1. Following abbreviation will be frequently used: walker [W], walker inhibitor [WI], track...)
 
 
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= System Design =
{{Template:DeoxyriboNucleicAwesomeHeader}}


==Domain Level Design==
= Progress 1: System Design =
 
==Design of the overall system ==


Overall domain level design is illustrated in figure 1. Following abbreviation will be frequently used: walker [W], walker inhibitor [WI], track 1 [TR1], probe for track 1 [PTR1], track 2 [TR2], probe for track 2 [PTR2], cargo 1 [C1], cargo attacher [CA], probe for cargo attacher [PCA], cargo goal inhibitor [CGI], cargo goal 1 [CG1], probe for cargo goal [PCG], walker goal [WG], and probe for walker goal [PWG].
Overall domain level design is illustrated in figure 1. Following abbreviation will be frequently used: walker [W], walker inhibitor [WI], track 1 [TR1], probe for track 1 [PTR1], track 2 [TR2], probe for track 2 [PTR2], cargo 1 [C1], cargo attacher [CA], probe for cargo attacher [PCA], cargo goal inhibitor [CGI], cargo goal 1 [CG1], probe for cargo goal [PCG], walker goal [WG], and probe for walker goal [PWG].


:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Domain Level Project Design|Domain Level Project Design]]''
With our overall design in mind, we must design DNA sequences, down to the base level, which undergo the interactions that we desire, without forming secondary structures and binding in unintended ways. We approach this through a combination of pre-generated noninteracting sequences, and trial-and-error design using NUPACK simulation software.
 


==Sequence Level Design==
Also, Random walking playground and cargo sorting playground were designed using a rectangular orgiami.
:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Sequence Design|Sequence Design]]''
With our overall design in mind, we must design DNA sequences, down to the base level, which undergo the interactions that we desire, without forming secondary structures and binding in unintended ways. We approach this through a combination of pre-generated noninteracting sequences, and trial-and-error design using NUPACK simulation software.


:''Main article about Domain Level Design: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Domain Level Project Design|Domain Level Project Design]]''


==Origami Layout==
:''Main article about Sequence Level Design: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Sequence Design|Sequence Design]]''


Random walking playground and cargo sorting playground were designed using a rectangular orgiami.
:''Main Article about Origami Layout Design: ''[[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Origami Layouts|List of Origami Layouts]]''


:Main Article: ''[[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Origami Layouts|List of Origami Layouts]]''
== Design of the experiments ==


We used three different experimental techniques, and here is the design of each experiments.


== Experimental Design==
1. Before constructing our origami and observing how it behaves, we run a large number of experiments observable through Gel Electrophoresis to verify that many of our mechanisms behave as we expect them to.


=== Verification of Mechanisms through Gel Experiments===
2. Various DNA strands are tagged with fluorophores and quenchers in order to investigate different mechanisms more directly, both in solution and on origami.  
:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/Gel Experiments|Gel Experiments]]''
Before constructing our origami and observing how it behaves, we run a large number of experiments observable through Gel Electrophoresis to verify that many of our mechanisms behave as we expect them to.  


:''Main article about design of the SPEX experiment: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/SPEX Experiments|SPEX Experiments Design]]''


=== Verification of Mechanisms through Fluorescent Spectroscopy===
3. Individual system is observed directly under AFM.
:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/SPEX Experiments|SPEX Experiments]]''
Various DNA strands were tagged with fluorophores and quenchers in order to investigate different mechanisms more directly, both in solution and on origami.  


:''Main article about desing of the AFM experiment: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/AFM Experiments Design|AFM Experiment Design]]''


=== Verification of Mechanisms through Atomic Force Microscopy===
:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/AFM Experiments Design|AFM Experiment]]''


:''Main article: [[Biomod/2011/Caltech/DeoxyriboNucleicAwesome/AFM Experiments|AFM Imaging]]''
{{Template:DeoxyriboNucleicAwesomeFooter}}
Walkers tagged with biotins were planted onto DNA origami, attempts were made to observe random walking on the origami directly under AFM.

Latest revision as of 09:27, 3 November 2011

Friday, April 19, 2024

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Progress 1: System Design

Design of the overall system

Overall domain level design is illustrated in figure 1. Following abbreviation will be frequently used: walker [W], walker inhibitor [WI], track 1 [TR1], probe for track 1 [PTR1], track 2 [TR2], probe for track 2 [PTR2], cargo 1 [C1], cargo attacher [CA], probe for cargo attacher [PCA], cargo goal inhibitor [CGI], cargo goal 1 [CG1], probe for cargo goal [PCG], walker goal [WG], and probe for walker goal [PWG].

With our overall design in mind, we must design DNA sequences, down to the base level, which undergo the interactions that we desire, without forming secondary structures and binding in unintended ways. We approach this through a combination of pre-generated noninteracting sequences, and trial-and-error design using NUPACK simulation software.

Also, Random walking playground and cargo sorting playground were designed using a rectangular orgiami.

Main article about Domain Level Design: Domain Level Project Design
Main article about Sequence Level Design: Sequence Design
Main Article about Origami Layout Design: List of Origami Layouts

Design of the experiments

We used three different experimental techniques, and here is the design of each experiments.

1. Before constructing our origami and observing how it behaves, we run a large number of experiments observable through Gel Electrophoresis to verify that many of our mechanisms behave as we expect them to.

2. Various DNA strands are tagged with fluorophores and quenchers in order to investigate different mechanisms more directly, both in solution and on origami.

Main article about design of the SPEX experiment: SPEX Experiments Design

3. Individual system is observed directly under AFM.

Main article about desing of the AFM experiment: AFM Experiment Design