| Literature DB >> 24736113 |
Michael Wright1, M Ameruddin Azhar2, Ahmed Kamal3, Andrew D Miller4.
Abstract
Recombinant Escherichia coli lysyl-tRNA synthase (LysU) has been previously utilised in the production of stabile, synthetic diadenosine polyphosphate (ApnA) analogues. Here we report on the extended use of a new recombinant histidine residue-tagged LysU as a tool for highly controlled phosphatephosphate bond formation between nucleotides, avoiding the need for complex protecting group chemistries. Resulting high yielding tandem LysU-based biosynthetic-synthetic/synthetic-biosynthetic strategies emerge for the preparation of varieties of ApnA analogues directly from inexpensive natural nucleotides and nucleosides. Analogues so formed make a useful small library with which to probe ApnA activities in vitro and in vivo leading to the discovery of new, potentially potent biopharmaceuticals active against chronic pain and other chronic, high-burden disease states.Entities:
Keywords: Analogues; Biosynthesis; Diadenosine polyphosphate; Dinucleoside polyphosphates; Lysyl tRNA synthetase (LysU)
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Year: 2014 PMID: 24736113 DOI: 10.1016/j.bmcl.2014.03.064
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823