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The effect of the osmolyte trimethylamine N‐oxide on the stability of the prion protein at low pH
Author(s) -
Granata Vincenzo,
Palladino Pasquale,
Tizzano Barbara,
Negro Alessandro,
Berisio Rita,
Zagari Adriana
Publication year - 2006
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.20481
Subject(s) - chemistry , osmolyte , trimethylamine , trimethylamine n oxide , protein stability , prion protein , oxide , biochemistry , organic chemistry , medicine , disease
A study of the effect of trimethylamine N‐oxide on the stability of two recombinant forms of the prion protein PrP, an ovine full‐length and a human truncated form, is here reported. Both thermal denaturation and denaturation at room temperature were analyzed at pH values above and below the pKa of trimethylamine N‐oxide, which is close to 4.7. Surprisingly, results showed that not only is trimethylamine N‐oxide able to decrease PrP thermal stability at low pH but it also acts as a strong denaturant at room temperature. Likely, this destabilization is due to the capability of the cationic form of trimethylamine N‐oxide to interact with the protein backbone as well as to weaken electrostatic interactions which are important for PrP fold. These results constitute the first experimental measurement of the effect of trimethylamine N‐oxide on PrP stability and provide an unambiguous proof of the destabilizing effect of this osmolyte on PrP at low pH. © 2006 Wiley Periodicals, Inc. Biopolymers 82: 234–240, 2006 This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com