Previous Page  87 / 92 Next Page
Information
Show Menu
Previous Page 87 / 92 Next Page
Page Background

- 86 -

Polymers and Self Assembly: From Biology to Nanomaterials Poster Session II

37-POS

Board 37

Mechanical Tightening and Untying of a Trefoil-Knotted Protein by Optical Tweezers

Maira Rivera

, Andrés Bustamante, Christian A. Wilson, Mauricio Baez.

Universidad de Chile, Santiago, Chile

According to the funnel hypothesis, the roughness of the energetic landscape increases along

with the topological complexity of proteins and thus, the chance of produce misfolded structures.

Knotted proteins are examples of topological complexity, but it is not clear how these proteins

deal with the folding because experimentally is difficult to determine how the folding

mechanism is coupled with the threading of the polypeptide chain.

To solve this problem, we have studied the mechanical unfolding of a trefoil knotted protein

(MJ0366 of

Methanocaldococcus jannaschii

) using the experimental setup of optical tweezers.

Two mutants were created, one to pull MJ0366 from the ends of the polypeptide chain to tight

the knot, and other mutant in order to untie the protein by pulling from key residues of the

structure. When the knot was tightened, MJ0366 showed a two state folding mechanism

characterized by the presence of a single unfolding and refolding transitions with average forces

of 19.8 pN and 13.6 pN respectively. The contour length was 7.8 nm shorter than expected. This

could be associated in part with the presence of the knot in the structure, although the formation

of trefoil knot decreases the contour length in about 5 nm. Free energy of unfolding reaction,

calculated using the Crooks fluctuation theorem, is 13.6 kcal/mol around 4.4 kcal/mol higher

than the obtained in experiments performed with chaotropic agents. In the case of the MJ0366

mutant whose knot is untied upon pulling, preliminary experiments show a complex folding

mechanism with multiple transitions of unfolding and refolding. These results suggest that

threading of the polypeptide chain creates a rougher landscape for folding, but once the knot is

formed, the folding landscape becomes smooth. Funded by Fondecyt: 1151274, Anillo ACT-

1107, CONICYT fellowship N°21130254.