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  4. Deoxyribozymes and bioinformatics: complementary tools to investigate axon regeneration

Deoxyribozymes and bioinformatics: complementary tools to investigate axon regeneration

Cell Tissue Res, 2012 · DOI: 10.1007/s00441-011-1291-6 · Published: December 22, 2011

NeurologyGeneticsBioinformatics

Simple Explanation

This review focuses on deoxyribozyme technology, a potential therapeutic for spinal cord injuries (SCIs) or other brain insults, combined with a bioinformatics approach to understand the complex protein-protein interactions that occur after such trauma. Bioinformatics helps identify key players in the complex processes after SCI and novel molecules against which new knockdown agents can be generated. Used synergistically, deoxyribozymes and bioinformatics should facilitate the pursuit of treatments for central nervous system insults.

Study Duration
Not specified
Participants
Not specified
Evidence Level
Review

Key Findings

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    Deoxyribozymes, also called DNA enzymes or DNAzymes, are single-stranded DNA molecules developed using systematic evolution of ligands by exponential enrichment (SELEX).
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    Modifications to deoxyribozymes, such as phosphorothioate linkages, 2′-O-methyl nucleotides, 3′-terminal nucleotide inversions, and locked nucleic acids, enhance bioactivity, lower toxicity, and increase target affinity.
  • 3
    Bioinformatics, particularly through microarray experiments and data mining, aids in identifying suitable target molecules for designing new deoxyribozymes to prevent regeneration failure after spinal cord injury.

Research Summary

This review discusses the potential of deoxyribozymes as therapeutic agents for central nervous system (CNS) trauma, particularly spinal cord injury (SCI), in conjunction with bioinformatics approaches. It covers the selection process, catalytic mechanisms, modifications, cellular uptake, and therapeutic applications of deoxyribozymes, comparing them with other knockdown technologies like ribozymes and siRNAs. The review highlights how bioinformatics can identify key molecules involved in SCI and suggests that a synergistic approach using both deoxyribozymes and bioinformatics could lead to better treatments for CNS injuries.

Practical Implications

Drug Development

Deoxyribozymes can be developed as therapeutic agents for neurological disorders, especially spinal cord injury.

Target Identification

Bioinformatics can be used to identify novel targets for therapeutic intervention in CNS trauma.

Synergistic Therapies

Combining deoxyribozymes with bioinformatics-driven approaches may lead to more effective treatments for paralysis.

Study Limitations

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