Further nuclease stabilization is achieved by substitution of 2?-OCH_{step three} for 2?-OH at purine positions. As the 2?-OCH₃ moiety is not compatible with current SELEX process enzymes, this alteration must occur during chemical synthesis following evolution of a specific aptamer sequence. Generally, most of the 2?-OH purines can be substituted without loss of binding activity. At some locations, purines cannot be substituted without loss of affinity. In addition to protection against endonucleases, it is useful to protect against 3? exonuclease activity. Therefore the 3? nucleotide is inverted to form a new 5?-OH, with a 3?-3? linkage to the penultimate base. Finally, synthesis incorporates nucleophilic amines or thiols, lending flexibility for attachment of the escorted species or other desirable modifications.

step 1 c. It’s a mass-decreased oligonucleotide you to exits the fresh SELEX process which will be truncated, after that protected against nucleases, and you may conjugated nutten Hessen so you can the cargo. Read more