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Solid-state NMR at natural isotopic abundance for the determination of conformational polymorphism - the case of designed β-turn peptides containing di-prolines.

Jayasubba Reddy YaravaRajesh SontiK KantharajuS RaghothamaKrishna Venkatachala Ramanathan
Published in: Chemical communications (Cambridge, England) (2018)
The proton double quantum-carbon single quantum correlation experiment has been applied to designed peptides in the solid state in natural isotopic abundance. Analogous to nOe studies in solution, through-space double-quantum connectivities have been exploited to obtain the cis-trans conformational polymorphism of diproline residues occurring at β-turns in the peptides.
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