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Author Topic: Approach for building G-quadruplex models with 3'-3' and 5'-5'polarity inversion  (Read 1822 times)

Offline muha

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Dear all,
I am working on the structural modeling of non-canonical G-quadruplexes (G4). Specifically, I am trying to build a monomolecular G4 model characterized by inversions of polarity (alternating 5'-3', 3'-3', 3'-5', and 5'-5' linkages) within the G-tracts.

I am looking for some guidance on how to build the starting structure: While DSSR is excellent at analyzing and rebuilding standard G4 topologies, i am not sure if it can handle these specific phosphodiester bond inversions.

Does DSSR have a built-in way to recognize and validate a chain that contains 3'-3' or 5'-5' linkages, or will it treat them as broken chains during analysis?
Are there specific commands in the latest DSSR releases (or via the mutate module) that allow for inverting the direction of a specific block of residues while maintaining the G-tetrad stacking geometry?

I am looking for a general methodology for handling these "inverted" backbone topologies in a way that remains compatible with subsequent Molecular Dynamics setups.
Once I find a stable workflow, I will be happy to summarize the steps for the community as per the forum guidelines.
Any suggestion is welcome!
Thank you for your time and for this useful resource.

Best

Offline xiangjun

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Hi muha,

Thanks for posting on the Forum, and sorry for the late reply.

I understand your aim to build a unimolecular G-quadruplex model with alternating 5'-3', 3'-3', 3'-5', and 5'-5' linkages. DSSR does not have a built-in option for building such models, and I am not aware of any other software that can do this. In my understanding, this would require a combination of DSSR and a 3D manual editing tool to adjust the polarity of the linkages.

As far as analysis is concerned, DSSR should be able to identify G-tetrads, and may take each tract as broken chains. We need specific examples to show how DSSR should behave in these cases. I will consider modifying DSSR to handle these cases if feasible.

Best regards,

Xiang-Jun
Dr. Xiang-Jun Lu[律祥俊](xiangjun@x3dna.org)
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