Crystal structures of 'ALternative Isoinformational ENgineered' DNA in B-form

The first structural model of duplex DNA reported in 1953 by Watson & Crick presented the double helix in B-form, the form that genomic DNA exists in much of the time. Thus, artificial DNA seeking to mimic the properties of natural DNA should also be able to adopt B-form. Using a host-guest syst...

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Veröffentlicht in:Philosophical transactions of the Royal Society of London. Series B. Biological sciences 2023-02, Vol.378 (1871), p.20220028
Hauptverfasser: Shukla, Madhura S, Hoshika, Shuichi, Benner, Steven A, Georgiadis, Millie M
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Sprache:eng
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Zusammenfassung:The first structural model of duplex DNA reported in 1953 by Watson & Crick presented the double helix in B-form, the form that genomic DNA exists in much of the time. Thus, artificial DNA seeking to mimic the properties of natural DNA should also be able to adopt B-form. Using a host-guest system in which Moloney murine leukemia virus reverse transcriptase serves as the host and DNA as the guests, we determined high-resolution crystal structures of three complexes including 5'-CTT AAG, 5'-CTT AAG and 5'-CTT AAG with 10 consecutive unnatural nucleobase pairs in B-form within self-complementary 16 bp duplex oligonucleotides. We refer to this ALternative Isoinformational ENgineered (ALIEN) genetic system containing two nucleobase pairs ( , pairing 2-amino-imidazo-[1,2- ]-1,3,5-triazin-(8 )-4-one with 6-amino-5-nitro-(1 )-pyridin-2-one, and , 6-amino-4-hydroxy-5-(1 )-purin-2-one with 3-methyl-6-amino-pyrimidin-2-one) as ALIEN DNA. We characterized both position- and sequence-specific helical, nucleobase pair and dinucleotide step parameters of and pairs in the context of B-form DNA. We conclude that ALIEN DNA exhibits structural features that vary with sequence. Further, can participate in alternative stacking modes within a similar sequence context as captured in two different structures. This finding suggests that ALIEN DNA may have a larger repertoire of B-form structures than natural DNA. This article is part of the theme issue 'Reactivity and mechanism in chemical and synthetic biology'.
ISSN:0962-8436
1471-2970
1471-2970
DOI:10.1098/rstb.2022.0028