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Development of selective DNA-interac...

Asamitsu, Sefan.

Development of selective DNA-interacting ligandsunderstanding the function of non-canonical DNA structures /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Development of selective DNA-interacting ligandsby Sefan Asamitsu.
其他題名:	understanding the function of non-canonical DNA structures /
作者:	Asamitsu, Sefan.
出版者:	Singapore :Springer Singapore :2020.
面頁冊數:	xiii, 111 p. :ill. (some col.), digital ;24 cm.
Contained By:	Springer Nature eBook
標題:	DNA-ligand interactions.
電子資源:	https://doi.org/10.1007/978-981-15-7716-1
ISBN:	9789811577161$q(electronic bk.)

Development of selective DNA-interacting ligandsunderstanding the function of non-canonical DNA structures /
Asamitsu, Sefan.

Development of selective DNA-interacting ligandsunderstanding the function of non-canonical DNA structures /[electronic resource] :by Sefan Asamitsu. - Singapore :Springer Singapore :2020. - xiii, 111 p. :ill. (some col.), digital ;24 cm. - Springer theses,2190-5053. - Springer theses..

1. General Introduction -- 2. Sequence-specific DNA alkylation and transcriptional inhibition by long-chain hairpin pyrrole-imidazole polyamide-chlorambucil conjugates targeting CAG/CTG trinucleotide repeats -- 3. Ligand-Mediated G-Quadruplex Induction in a Double-Stranded DNA Context by Cyclic Imidazole/Lysine Polyamide -- 4. Simultaneous Binding of Hybrid Molecules Constructed with Dual DNA-Binding Components to a G-Quadruplex and Its Proximal Duplex.

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.

ISBN: 9789811577161$q(electronic bk.)

Standard No.: 10.1007/978-981-15-7716-1doiSubjects--Topical Terms:

200705
DNA-ligand interactions.

LC Class. No.: QP624.74

Dewey Class. No.: 572.86

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520 $a 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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