Literature DB >> 18188766

Synthesis and stability of novel terminal phosphate-labeled nucleotides.

Bambi Reynolds1, Rachel Miller, John G Williams, Jon P Anderson.   

Abstract

Novel compounds consisting of a nucleotide triphosphate labeled with a PEG linker and various terminal groups attached to the gamma-phosphate of the nucleotide were constructed for use in efforts to produce a new class of DNA sequencer. The stability of these novel compounds was investigated to determine their utility as sequencing reagents. Hydrolysis rate constants were measured for both the natural nucleoside triphosphate dATP and novel dATP derivatives. The gamma-labeled dATP was approximately 20-fold more stable to hydrolysis than dATP.

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Year:  2008        PMID: 18188766     DOI: 10.1080/15257770701571768

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  3 in total

Review 1.  The challenges of sequencing by synthesis.

Authors:  Carl W Fuller; Lyle R Middendorf; Steven A Benner; George M Church; Timothy Harris; Xiaohua Huang; Stevan B Jovanovich; John R Nelson; Jeffery A Schloss; David C Schwartz; Dmitri V Vezenov
Journal:  Nat Biotechnol       Date:  2009-11-06       Impact factor: 54.908

2.  Fluorescent structural DNA nanoballs functionalized with phosphate-linked nucleotide triphosphates.

Authors:  Jon P Anderson; Bambi L Reynolds; Kristin Baum; John G Williams
Journal:  Nano Lett       Date:  2010-03-10       Impact factor: 11.189

3.  Polymerase synthesis of four-base DNA from two stable dimeric nucleotides.

Authors:  Michael G Mohsen; Debin Ji; Eric T Kool
Journal:  Nucleic Acids Res       Date:  2019-10-10       Impact factor: 16.971

  3 in total

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