Thionucleoside disulfide cross-linked duplex DNA
β Scribed by Robert S. Coleman; Jason L. McCary; Ronelito J. Perez
- Book ID
- 104260652
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 254 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A strategy for covalent cross-linking of duplex oligonucleotides is described, and is based on a direct base-to-base disulfide bond formed by iodine oxidation of two appropriately positioned thionucleoside bases. Cross-link formation between 4-thio-2'-deoxyuridine and 6-thio-2'-deoxyinosine is demonstrated in three sequence contexts (3' to 3', 5' to 5', or opposed).
π SIMILAR VOLUMES
Full details of a new strategy for cross-linking of duplex oligonucleotides are described. A direct base-to-base disulfide bond is formed by oxidation of two appropriately positioned thionucleoside bases. Cross-link formation between 4-thio-2'-deoxyuridine and 6-thio-2'-deoxyinosine is demonstrated
A new disulfide cross-linking strategy was developed to prepare hyaluronic acid (HA) hydrogel from thiolmodified HA. First, dithiobis(propanoic dihydrazide) (DTP) and dithiobis(butyric dihydrazide) (DTB) were synthesized and then coupled to HA with carbodiimide chemistry. Next, disulfide bonds of th