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Microbiology & Virology 2018

J u n e 2 1 - 2 2 , 2 0 1 8

P a r i s , F r a n c e

Page 32

Archives of Clinical Microbiology

ISSN 1989-8436

E u r o S c i C o n C o n f e r e n c e o n

Microbiology &

Virology

T

he emerging future of antisense oligonucleotides depends on rational

modifications of its nucleotide repeating units. Currently themost prevalent

design features that are crucial for continued antisense development are

nuclease resistance, cellular uptake, hybridization properties, and disruption

of RNA functions through terminating events.Very few structure-activity

relationship (SAR) studies have been directed to these problems and these

have typically used binding affinities and nuclease sensitivities as activity

end points rather than in vitro or in vivo biological activities. Further SAR

studies may be approached by sequence selection SARs which hold a certain

uniform modification type constant (e.g. phosphorothioates) while varying

the sequence of the oligonucleotide.The more traditional approach is to

modify the oligonucleotide while keeping the sequence constant. This review

is concerned with the latter approach and summarizes modifications of

the phosphorus atom, pentofuranosyl (sugar) linker, pentofuranosyl ring and

its 2'-substituents, and the heterocycles. The review covers the 1989-91

literature of various modified oligonucleotides designed and synthesized

to enhance pharmacokinetic and pharmacodynamic properties of antisense

oligonucleotides.

Keywords-

oligonucleotides, nuclease, RNA, SAR, pentofuranosyl, hetercycles.

Biography

Mohammed Sissaoui has completed his Master's degree In

Biochemistry & Molecular Biology at the age of 30 years from

The University Of Biskra - Algeria. He is a Medical Laborotry Sci-

entist At the Hospital Of Taoura Souk Ahras - Algeria, and

has been serving as a Medical Laboratory Technologist at

The Hemodialysis Clinic Souk Ahras - Algeria.

sissaoui_mohammed@yahoo.com

Anti-cancer Drug Design

M.SISSAOUI

University of Biskra, Algeria

M.SISSAOUI, Arch Clin Microbiol 2018 Voulume: 9

DOI: 10.4172/1989-8436-C3-011