Formation of a pseudoknot in the conserved RNA core domain in the
ribonucleoprotein human telomerase is required for function. In vitro
experiments show that the pseudoknot (PK) is in equilibrium with an extended
hairpin (HP) structure. We use molecular simulations of a coarse-grained model,
which reproduces most of the salient features of the experimental melting
profiles of PK and HP, to show that crowding enhances the stability of PK
relative to HP in the wild type and in a mutant associated with dyskeratosis
congenita. In monodisperse suspensions, small crowding particles increase the
stability of compact structures to a greater extent than larger crowders. If
the sizes of crowders in a binary mixture are smaller than the unfolded RNA,
the increase in melting temperature due to the two components is additive. In a
ternary mixture of crowders that are larger than the unfolded RNA, which mimics
the composition of ribosome, large enzyme complexes and proteins in E. coli,
the marginal increase in stability is entirely determined by the smallest
component. We predict that crowding can restore partially telomerase activity
in mutants, which dramatically decrease the PK stability.Comment: File "JACS_MAIN_archive_PDF_from_DOC.pdf" (PDF created from DOC)
contains the main text of the paper File JACS_SI_archive.tex + 7 figures are
the supplementary inf