The synthesis and evaluation of several novel antisense DNA analogs are proposed. Antisense oligodeoxynucleotides 15 to 20 nucleotides in length have been shown previously by other workers to inhibit tumor cell growth and viral growth. Design features of the proposed DNA analogs include: (1) the elimination of the metal ion that normally neutralizes the phosphate charge to promote entry into cells, and (2) the placement of a bulky group on the nucleotides to confer resistance to nucleases. Several modified oligodeoxynucleotides will be synthesized. Their following properties will be determined: 1) ability to hybridize with complementary, natural oligonucleotides as monitored by changes in ultraviolet absorbance with changes in temperature, 2) ability to resist nucleases in vitro, and 3) ability to inhibit human immunodeficiency virus in vivo.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29GM047375-04
Application #
2184784
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1992-06-01
Project End
1997-05-31
Budget Start
1995-06-01
Budget End
1996-05-31
Support Year
4
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Chemistry
Type
Schools of Earth Sciences/Natur
DUNS #
City
Riverside
State
CA
Country
United States
Zip Code
92521
Bain, J D; Switzer, C (1992) Regioselective ligation of oligoribonucleotides using DNA splints. Nucleic Acids Res 20:4372