Academic Journal
The 2‐Amino Group of 8‐Aza‐7‐deaza‐7‐bromopurine‐2,6‐diamine and Purine‐2,6‐diamine as Stabilizer for the Adenine–Thymine Base Pair in Heterochiral DNA with Strands in Anomeric Configuration
العنوان: | The 2‐Amino Group of 8‐Aza‐7‐deaza‐7‐bromopurine‐2,6‐diamine and Purine‐2,6‐diamine as Stabilizer for the Adenine–Thymine Base Pair in Heterochiral DNA with Strands in Anomeric Configuration |
---|---|
المؤلفون: | Chai, Yingying, Kondhare, Dasharath, Zhang, Aigui, Leonard, Peter, Seela, Frank |
المصدر: | Chemistry – A European Journal ; volume 27, issue 6, page 2093-2103 ; ISSN 0947-6539 1521-3765 |
بيانات النشر: | Wiley |
سنة النشر: | 2020 |
المجموعة: | Wiley Online Library (Open Access Articles via Crossref) |
الوصف: | Stabilization of DNA is beneficial for many applications in the fields of DNA therapeutics, diagnostics, and materials science. Now, this phenomenon is studied on heterochiral DNA, an autonomous DNA recognition system with complementary strands in α‐D and β‐D configuration showing parallel strand orientation. The 12‐mer heterochiral duplexes were constructed from anomeric (α/β‐D) oligonucleotide single‐strands. Purine‐2,6‐diamine and 8‐aza‐7‐deaza‐7‐bromopurine‐2,6‐diamine 2′‐deoxyribonucleosides having the capability to form tridentate base pairs with dT were used to strengthen the stability of the dA–dT base pair. T m data and thermodynamic values obtained from UV melting profiles indicated that the 8‐aza‐7‐deaza 2′‐deoxyribonucleoside decorated with a bromo substituent is so far the most efficient stabilizer for heterochiral DNA. Compared with that, the stabilizing effect of the purine‐2,6‐diamine 2′‐deoxyribonucleoside is low. Global changes of helix structures were identified by circular dichroism (CD) spectra during melting. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
DOI: | 10.1002/chem.202004221 |
الاتاحة: | http://dx.doi.org/10.1002/chem.202004221 https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004221 https://onlinelibrary.wiley.com/doi/full-xml/10.1002/chem.202004221 |
Rights: | http://creativecommons.org/licenses/by/4.0/ |
رقم الانضمام: | edsbas.1EEC40B9 |
قاعدة البيانات: | BASE |
DOI: | 10.1002/chem.202004221 |
---|