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Author Topic: Circular DNA parameters  (Read 154 times)

Offline heesch

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Circular DNA parameters
« on: October 30, 2020, 01:27:01 pm »
Dear Dr. Xiang-Jun Lu,

Thank you for developing (and maintaining) this collection of beautiful and practical DNA geometry software!

For my project I want to generate circular DNA (plasmids) of various sizes.
Based on the book chapter of Calladine et al. (see source below) I found a way to determine the base roll angle for each base pair.

For example, we can determine the curvature of each helical turn to make a circle consisting of 100 bp as follows:

- assume 10 bp per turn
- assume helix angle of 36 degrees

First determine number of turns: 10
Determine the angle each turn has to make: 36 degrees
For a smooth transition per base step fit this angle to cosine:

First we need to determine the amplitude to account for +/- direction of helix
amplitude = 36 / (10*0.5)

Then each roll angle can be determined as follows:
for bp_i in range[0:100]:
   roll_angle = amplitude*(cos(helix_angle)*bp_i))

which gives you periodic values of:
[7.2, 5.825, 2.225, -2.225, -5.825, -7.2, -5.825, -2.225,  2.225, 5.825, ....]

Of course this (could) work for an arbitrary length of sequences.
So may plan was to use these roll angle parameters to make circular DNA.

 
As a starting point I just used for each bp a twist and rise value of 36 and 3.34 respectively (since I want B-DNA) together with the periodic roll angle values and all other parameters black (zero). See attachement for parameter file.

When I visualize the structure with the rebuilder at the webserver (http://web.x3dna.org/custom/option) the result is very close to perfect, see image in attachement. However, the ring is not perfectly planar (although I want to have the geometry completely planar such that I can easily define the connections of the beginning and end in the pdb later on). 

I very much hope that with your years of DNA geometry experience you could provide some insight on how to make the ring perfectly planar. I am probably overlooking something obvious... So apologies in advance if the question is unclear!

Thank you for reading my message and stay safe!

Best,
Thor

PS
Eventually I want to make this to work for arbitrary length of sequences, however, conceptually I couldn't think of a smart way to deal with the decimal numbers arising in the total number of "complete" turns. I guess one should start to introduce varying helix twists such that the outer ends properly meet?

Source: Calladine, C.R., Drew, H.R., Luisi, B.F. & Travers, A.A. Understanding DNA: theMolecule and How It WorksChapter 4 (Elsevier Academic Press, San Diego, CA,2004).
« Last Edit: October 30, 2020, 01:28:41 pm by heesch »

Offline xiangjun

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Re: Circular DNA parameters
« Reply #1 on: October 30, 2020, 03:46:34 pm »
Dear Thor,

Thanks for your insightful questions on building perfectly circular DNAs of various sizes. DNA/RNA modeling is a topic of great significance and there is clearly a lack of practical software tools. I'm interested in developing new modeling features in DSSR, a replacement of the classic 3DNA suite of programs. Nevertheless ...

Quote
Thank you for developing (and maintaining) this collection of beautiful and practical DNA geometry software!
I've enjoyed maintaining 3DNA for nearly two decades. With NIH funding support over the past 9 years, I created DSSR as a replacement of 3DNA v2.x. Alas, I am now out of luck to continuously serve the community for free via NIH funding support, as it used to be.

DSSR is now licensed by Columbia University. Please buy a license if users find 3DNA/DSSR useful and my service valuable. Think in terms of the time/efforts you would otherwise have to spend. Further support and development of DSSR (including customized applications) will be devoted to paid users only -- that's the new normal.

Best regards,

Xiang-Jun


« Last Edit: November 10, 2020, 11:13:34 am by xiangjun »
Dr. Xiang-Jun Lu [律祥俊]
Email: xiangjun@x3dna.org
Homepage: http://x3dna.org/
Forum: http://forum.x3dna.org/

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Created and maintained by Dr. Xiang-Jun Lu [律祥俊] (xiangjun@x3dna.org)
The Bussemaker Laboratory at the Department of Biological Sciences, Columbia University.