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      Permanent link:
      https://www.ias.ac.in/article/fulltext/jbsc/014/03/0319-0328

    • Keywords

       

      Interaction energy; nucleoside analogues; transcription; incorporation and inhibition

    • Abstract

       

      The quantum mechanical perturbation method has been utilized to study the biological activity of 8-azapurine (8-azaguanosine, 8-azaadenosine and 8-aza-2,6-diamino-purine) nucleoside antibiotics. The in-plane (hydrogen bonding) and stacking energy of 8-azapurine bases have been evaluated with nucleic acid bases and base pairs in all possible orientations. The energy values and the sites of association of analogous bases, obtained by optimization of energy values as well as the sites of association of nucleic acid bases during the transcription process have been compared. The model developed earlier for the incorporation of nucleoside analogues has been used to find out the inhibitory effects of the drug on nucleic acid and protein synthesis. It has been observed that the activity of 8-azapurines are of the following order

      8-azaguanine > 8-aza-2,6-diaminopurine > 8-azaadenine

      and these analogues show preference for binding near a guanine or cytosine in the chain. The results are in agreement with the experimental observations

    • Author Affiliations

       

      Rajendra Prasad Ojha1 Nitish K Sanyal1

      1. Department of Physics, University of Gorakhpur, Gorakhpur - 273 009, India
    • Dates

       
  • Journal of Biosciences | News

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      Plant mitochondria are quite distinct and have unique features, such as a cyanide-insensitive alternate pathway. They also interact with chloroplasts to optimize photosynthetic carbon assimilation.


      Submissions are welcome until 30 July 2023. The contributions can be original articles, short communications, reviews, or mini-reviews on any topic related to plant mitochondria.


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      Posted on April 12, 2023
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