Transition state heterogeneity in GCN4 coiled coil folding studied by using multisite mutations and crosslinking.
Transition state heterogeneity in GCN4 coiled coil folding studied by using multisite mutations and crosslinking.
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DOI:
10.1073/pnas.96.19.10699
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发表时间:
1999-09
影响因子:
11.1
通讯作者:
Liam B. Moran;Joel P. Schneider;A. Kentsis;Giridher A. Reddy;T. Sosnick
中科院分区:
文献类型:
--
作者:
Liam B. Moran;Joel P. Schneider;A. Kentsis;Giridher A. Reddy;T. Sosnick
We have investigated the folding behavior of dimeric and covalently crosslinked versions of the 33-residue alpha-helical GCN4-p1 coiled coil derived from the leucine zipper region of the transcriptional activator GCN4. The effects of multisite substitutions indicate that folding occurs along multiple routes with nucleation sites located throughout the protein. The similarity in activation energies of the different routes together with an analysis of intrinsic helical propensities indicate that minimal helix is present before a productive collision of the two chains. However, approximately one-third to one-half of the total helical structure is formed in the postcollision transition state ensemble. For the crosslinked, monomeric version, folding occurs along a single robust pathway. Here, the region nearest the crosslink, with the least helical propensity, is structured in the transition state whereas the region farthest from the tether, with the most propensity, is completely unstructured. Hence, the existence of transition state heterogeneity and the selection of folding routes critically depend on chain topology.