Novel Substrates for Kinases Involved in the Biosynthesis of Inositol Pyrophosphates and Their Enhancement of ATPase Activity of a Kinase.

IP6K and PPIP5K are two kinases involved in the synthesis of inositol pyrophosphates. Synthetic analogs or mimics are necessary to understand the substrate specificity of these enzymes and to find molecules that can alter inositol pyrophosphate synthesis. In this context, we synthesized four scyllo-inositol polyphosphates-scyllo-IP5, scyllo-IP6, scyllo-IP7 and Bz-scyllo-IP5-from myo-inositol and studied their activity as substrates for mouse IP6K1 and the catalytic domain of VIP1, the budding yeast variant of PPIP5K. We incubated these scyllo-inositol polyphosphates with these kinases and ATP as the phosphate donor. We tracked enzyme activity by measuring the amount of radiolabeled scyllo-inositol pyrophosphate product formed and the amount of ATP consumed. All scyllo-inositol polyphosphates are substrates for both the kinases but they are weaker than the corresponding myo-inositol phosphate. Our study reveals the importance of axial-hydroxyl/phosphate for IP6K1 substrate recognition. We found that all these derivatives enhance the ATPase activity of VIP1. We found very weak ligand-induced ATPase activity for IP6K1. Benzoyl-scyllo-IP5 was the most potent ligand to induce IP6K1 ATPase activity despite being a weak substrate. This compound could have potential as a competitive inhibitor.

Topochemical synthesis of different polymorphs of polymers as a paradigm for tuning properties of polymers.

Different packing is a mechanism through which nature can produce materials of different properties from the same basic units. There is great interest in constructing different forms of the same polymer by utilising different packing. Common solution-synthesized polymers are amorphous and their post-synthesis crystallization into different topologies is almost impossible. Here we show solid-state polymerization of different reactive polymorphs of a monomer pre-organized in different topologies. Trimorphs of a dipeptide monomer pack in a head-to-tail fashion, placing the azide and alkyne of adjacent monomers in proximity. On heating, these crystals undergo a topochemical azide-alkyne cycloaddition reaction yielding triazole-linked polymer in three different crystalline states; one with antiparallel arrangement of polymer chains, another with parallelly oriented chains, and a third form containing a 1:1 blend of two different conformers aligned in parallel. This approach of exploiting different polymorphs of a monomer for topochemical polymerization to yield polymorphs of polymers is promising for future research.

Synthesis and Reversible Hydration of a Pseudoprotein, a Fully Organic Polymeric Desiccant by Multiple Single-Crystal-to-Single-Crystal Transformations.

A diphenylalanine derivative, N3-Phe-Phe-NHCH2CCH, was designed for topochemical azide-alkyne cycloaddition (TAAC) polymerization. This dipeptide adopted ß-sheet arrangement as designed, in its crystals, but the azide and alkyne were not fitly aligned for their topochemical reaction. However, the voids present around these groups allowed them to attain a reactive geometry upon heating and their consequent TAAC polymerization to a pseudoprotein in a single-crystal-to-single-crystal (SCSC) fashion. This motion led to the creation of channels in the product crystal and it absorbed water from the surroundings to fill these channels as H-bonded water wire. The pseudoprotein undergo reversible hydration/dehydration in SCSC fashion many times under mild conditions: hydration at low relative humidity and dehydration at low temperature. Vapor sorption analyses suggest that this fully organic polymer might be useful as an energy-efficient desiccant material for controlling indoor humidity.

Bio-inspired synthesis of rare and unnatural carbohydrates and cyclitols through strain driven epimerization.

We report a bio-inspired, strain driven epimerization of trans-ketals to cis-ketals through an enolate intermediate. Swern oxidation of a hydroxyl group adjacent to a trans-ketal effects both oxidation and its epimerization to cis-ketal. This novel and general strategy allows inversion of up to three contiguous stereocenters and has been illustrated by the synthesis of several unnatural/rare isomers of carbohydrates/cyclitols from their naturally abundant isomers.