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Nucleic acid sequencing nucleobases

The amino acid sequence of our first aPNA (which we termed backbone 1 or bl) was designed based on this amphipathic hehx sequence (Fig. 5.3 B). Specifically, this aPNA backbone included hydrophobic amino acids (Ala and Aib), internal salt bridges (Glu-(aa)3-Lys-(aa)3-Glu), a macrodipole (Asp-(aa)i5-Lys), and an N-ace-tyl cap to favor a-helix formation. The C-termini of these aPNA modules end in a carboxamide function to preclude any potential intramolecular end effects. Each aPNA module incorporates five nucleobases for Watson-Crick base pairing to a target nucleic acid sequence. [Pg.199]

When two nucleic acid strands have complementary nucleic acid sequence, they can undergo hybridization to form double-stranded duplex structures. DNA forms a double-stranded helix composed of two complementary helical polynucleotide chains, aligned antiparallel, which are coiled around a common axis. In helix form, the anionic backbone lies on the outside of the structure with the nucleobases in the core, perpendicular to the axis and separated by a distance of 3.4 A. This B-form helix (Figure 2a) has a right-handed coil that repeats itself every 34 A with a turn every... [Pg.3188]

However both classes, nucleic acids and proteins, are linear polymers in which the linear (nucleobase or amino acid) sequence encodes the three-dimensional structure and function of the polymer. [Pg.153]

Interestingly, the emission of [Pt(tpy)(OH)]+ is quenched in water, but is restored upon intercalation with double-stranded nucleic acids [poly(dA-dT)]2 and [poly(dI-dC)]2 [73]. Although intercalation can also occur at G-C-rich sequences - and indeed it does so more strongly than for A-T - emission is then quenched by electron-transfer from guanine, the most readily oxidized of the nucleobases. The initial intercalative interactions are probably followed by covalent platination of the DNA, most likely by purine-N7 displacing the OH ligand, reminiscent of cisplatin. The absorption... [Pg.239]

Type III system. DNA synthesis inside fatty acid vesicles. DNA is today the cellular macromolecule where the information about the proteins sequence is stored as ordered nucleobases sequence. DNA is thought to appear later than RNA in the molecular evolution, mainly with the function of storage. Its minor reactivity (due to loss of 2 -OH group) favour its chemical stability. The use of DNA polymerization in vesicle-based cell models aims to demonstrate how nucleic acids can be synthesized inside compartments, again in an origin-of-life perspective. However, due to the recent developments of DNA-based biotechnologies, it is possible that DNA-reactions in micro- or submicro-compartments... [Pg.481]

Peptide nucleic acid (PNA) was introduced by Nielsen and coworkers, and is a chimera of DNA nucleobases with a peptide backbone (see also section 3.1 on ohgonucleotide-peptide conjugates). PNA is based on an aminoethyl-glycine backbone (18), and is therefore neutral. PNA binds tightly to complementary nucleic add, and is resistant to nucleases. One drawback of PNA is that sequences are often insoluble, and one way to resolve this is to include a lysine taU onto the PNA. Reports on PNA during this review period include new synthetic approaches, a number of new analogues as well as many novel apphcations. [Pg.184]


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See also in sourсe #XX -- [ Pg.15 , Pg.16 ]




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