A list of puns related to "Nucleic acid analogue"
Artificial Nucleic Acid Analogue Substitutes, or ANAAS as they are known, or colloquially Pineapples due to the Latin and Germanic similarity linguistically, they have multiple uses, such as:
Nucleic acid analogues are compounds which are structurally similar to naturally occurring RNA and DNA, used in medicine and in molecular biology research. An analogue may have any specification of these altered. Examples include universal bases, which can pair with all four canon bases, and phosphate-sugar backbone analogues such as PNA, which affect the properties of the chain (PNA can even form a triple helix). Nucleic acid analogues are also called Xeno Nucleic Acid and represent one of the main pillars of xenobiology, the design of new-to-nature forms of life based on alternative biochemistries.
This could potentially pave the way into developing lab grown animals, lifeforms and possible even humans. The potential is unlimited, we merely have to open our eyes to the wonders that Nano-Afrika can bring us.
I can recogonize them if shown them, but I have been really struggling to draw them out precisely. Like I know I can draw out the rough features and I know how to differentiate between them.
Important updates to this post including that a clinical trial was based on "misreported data" and the fact #Exicure CEO David Giljohann, one of the developers of the #SphericalNucleicAcids in Chad Mirkin's group is "separating" from the company.
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Nucleic acids are chemically modified to fine-tune their properties for biological function. Chemical tools for selective tagging of base modifications enables new approaches; the photosensitizers riboflavin and anthraquinone were previously proposed to oxidize N6-methyladenine (m6A) or 5-methylcytosine (5mdC) selectively. Herein, riboflavin, anthraquinone, or Rose Bengal were allowed to react with the canonical nucleosides dA, dC, dG, and dT, and the modified bases 5mdC, m6A, 8-oxoguanine (dOG), and 8-oxoadenine (dOA) to rank their reactivities. The nucleoside studies reveal that dOG is the most reactive and that the native nucleoside dG is higher or similar in reactivity to 5mdC or m6A; competition in both single- and double-stranded DNA of dG vs. 5mdC or 6mdA for oxidant confirmed that dG is favorably oxidized. Thus, photosensitizers are promiscuous nucleic acid oxidants with poor chemoselectivity that will negatively impact attempts at targeted oxidation of modified nucleotides in cells.
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