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Molten globule nature of Plasmodium falciparum P2 homo-tetramer.

ABSTRACT: The P2 protein in Plasmodium falciparum has a high tendency to oligomerize, which seems to drive many of its non-ribosomal functions. During nuclear division of the parasite inside RBC, P2 translocates to the RBC surface as a tetramer. From a systematic study using variety of biophysical techniques, NMR spectral characteristics and relaxation dispersion measurements under different conditions of pH and/or urea concentrations, we deduce that (i) PfP2, an almost entirely helical protein, forms a molten globule monomer at low pH, (ii) at physiological pH, and at micro-molar concentrations, PfP2 is a stable tetramer wherein two dimmers associate sideways with close packing of helices at the interface, and (iii) the molten globule characteristic of the monomer is preserved in the tetramer. This dynamism in the structure of PfP2 may have functional implications since it is known that different kinds of oligomers are transiently formed in the parasite.

SUBMITTER: Mishra P

PROVIDER: S-EPMC5668626 | biostudies-literature | 2015 May

REPOSITORIES: biostudies-literature

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Molten globule nature of <i>Plasmodium falciparum</i> P2 homo-tetramer.

Mishra Pushpa P Choudhary Sinjan S Mukherjee Sujoy S Sengupta Disha D Sharma Shobhona S Hosur Ramakrishna V RV

Biochemistry and biophysics reports 20150330

The P2 protein in <i>Plasmodium falciparum</i> has a high tendency to oligomerize, which seems to drive many of its non-ribosomal functions. During nuclear division of the parasite inside RBC, P2 translocates to the RBC surface as a tetramer. From a systematic study using variety of biophysical techniques, NMR spectral characteristics and relaxation dispersion measurements under different conditions of pH and/or urea concentrations, we deduce that (i) PfP2, an almost entirely helical protein, fo ...[more]

PMID: 29124138

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