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. 2012 Sep 26;134(38):15652-5.
doi: 10.1021/ja3063088. Epub 2012 Sep 13.

Strong contributions from vertical triads to helix-partner preferences in parallel coiled coils

Jay D Steinkruger  1 , Gail J Bartlett, Derek N Woolfson, Samuel H Gellman
Affiliations

Strong contributions from vertical triads to helix-partner preferences in parallel coiled coils

Jay D Steinkruger et al. J Am Chem Soc. .

Abstract

Pairing preferences in heterodimeric coiled coils are determined by complementarities among side chains that pack against one another at the helix-helix interface. However, relationships between dimer stability and interfacial residue identity are not fully understood. In the context of the "knobs-into-holes" (KIH) packing pattern, one can identify two classes of interactions between side chains from different helices: "lateral", in which a line connecting the adjacent side chains is perpendicular to the helix axes, and "vertical", in which the connecting line is parallel to the helix axes. We have previously analyzed vertical interactions in antiparallel coiled coils and found that one type of triad constellation (a'-a-a') exerts a strong effect on pairing preferences, while the other type of triad (d'-d-d') has relatively little impact on pairing tendencies. Here, we ask whether vertical interactions (d'-a-d') influence pairing in parallel coiled-coil dimers. Our results indicate that vertical interactions can exert a substantial impact on pairing specificity, and that the influence of the d'-a-d' triad depends on the lateral a' contact within the local KIH motif. Structure-informed bioinformatic analyses of protein sequences reveal trends consistent with the thermodynamic data derived from our experimental model system in suggesting that heterotriads involving Leu and Ile are preferred over homotriads involving Leu and Ile.

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Figures

Figure 1
Figure 1
Orthogonal views of an a knob (green) into hole (blue residues) interaction from an experimentally determined protein structure (PDB 2ZTA). Images were generated using PyMOL
Figure 2
Figure 2
(A) Sequence of parallel coiled-coil model system CT-C’SG (SG = Second Generation). Succ = N-terminal succinyl group. (B) Helical wheel and net diagrams of CT-C’SG
Figure 3
Figure 3
Partial helical net diagrams for CT-C’SG and three mutants used to calculate the discrimination energy (DE). The DE value was derived from the thermodynamic data in Table S2 of the supporting information.
See this image and copyright information in PMC

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