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Development of Selective DNA-Interacting Ligands - Understanding the Function of Non-canonical DNA Structures (Paperback, 1st ed. 2020)
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Development of Selective DNA-Interacting Ligands - Understanding the Function of Non-canonical DNA Structures (Paperback, 1st ed. 2020)
Series: Springer Theses
Expected to ship within 10 - 15 working days
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This book addresses the development of both DNA-sequence-selective
and DNA-form-selective ligands, with the aim of creating potential
molecular probes and therapeutic agents for non-canonical DNA
structure-caused human diseases. Over the past two decades, the
structural diversity of DNA forms has been proven to have profound
implications in various biological, neurological, and
pharmacological events. In response, researchers have since made
tremendous efforts to obtain highly active drugs interacting with
disease-related non-canonical DNA structures. These drugs, however,
have not yet been approved for clinical use. One obstacle impeding
their clinical application has to do with selectivity. This book
focuses on secondary DNA structures formed by trinucleotide repeat
sequences ("hairpin form") or guanine-rich sequences ("G-quadruplex
form"), both of which are pathological molecules for
neurodegenerative diseases and/or cancer. Most importantly, it
contends that a particular secondary structure of DNA in the
context of the human genome can be targeted with a minimal affinity
to other DNA structures by means ofcareful and rational ligand
design. This approach opens an avenue to the development of highly
selective drugs or diagnostic chemical tools for human diseases.
Readers who want to know how synthetic ligands can be designed to
selectively target a certain DNA molecule will find this book
highly informative.
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