Zimm-Bragg model

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In statistical mechanics, the Zimm-Bragg model is a helix-coil transition model that describes helix-coil transitions of macromolecules, usually polymer chains. Most models provide a reasonable approximation of the fractional helicity of a given polypeptide; the Zimm-Bragg model differs by incorporating the ease of propagation with respect to nucleation.

1 Helix-coil transition models
2 Zimm-Bragg
3 Statistical mechanics
4 See also
5 References

[edit] Helix-coil transition models

Helix-coil transition models assume that polypeptides are linear chains composed of interconnected segments. Further, models group these sections into two broad categories: coils, random conglomerations of disparate unbound pieces, are represented by the letter 'C', and helices, ordered states where the chain has assumed a structure stabilized by hydrogen bonding, are represented by the letter 'H'.^[1]

Thus, it is possible to loosely represent a macromolecule as a string such as CCCCHCCHCHHHHHCHCCC and so forth. The number of coils and helices factors into the calculation of fractional helicity, $\theta \$ , defined as

$\theta = \frac{\left \langle i \right \rangle}{N}$

where

$\left \langle i \right \rangle \$ is the average helicity and

$N \$ is the number of helix or coil units.

[edit] Zimm-Bragg

Dimer sequence	Statistical weight
$...CC... \$	$1 \$
$...CH... \$	$\sigma s \$
$...HC... \$	$\sigma s \$
$...HH... \$	$\sigma s^2 \$

The Zimm-Bragg model takes the cooperativity of each segment into consideration when calculating fractional helicity. The probability of any given monomer being a helix or coil is affected by which the previous monomer is; that is, whether the new site is a nucleation or propagation.

By convention, a coil unit ('C') is always of statistical weight 1. Addition of a helix state ('H') to a previously coiled state (nucleation) is assigned a statistical weight $\sigma s \$ , where $\sigma \$ is the nucleation parameter and

$s = \frac{[H]}{[C]}$ .

Adding a helix state to a site that is already a helix (propagation) has a statistical weight of $s \$ . For most proteins,

$s \ll 1 < \sigma \$

which makes the propagation of a helix more favorable than nucleation of a helix from coil state.^[2]

From these parameters, it is possible to compute the fractional helicity $\theta \$ . The average helicity $\left \langle i \right \rangle \$ is given by

$\left \langle i \right \rangle = \left(\frac{s}{q}\right)\frac{dq}{ds}$

where $s \$ is the statistical weight and $q \$ is the partition function given by the sum of the probabilities of each site on the polypeptide. The fractional helicity is thus given by the equation

$\theta = \frac{1}{N}\left(\frac{s}{q}\right)\frac{dq}{ds}$ .

[edit] Statistical mechanics

The Zimm-Bragg model is equivalent to a one-dimensional Ising model and has no long-range interactions, i.e., interactions between residues well separated along the backbone; therefore, by the famous argument of Rudolf Peierls, it cannot undergo a phase transition.

The statistical mechanics of the Zimm-Bragg model^[3] may be solved exactly using the transfer-matrix method. The two parameters of the Zimm-Bragg model are σ, the statistical weight for nucleating a helix and s, the statistical weight for propagating a helix. These parameters may depend on the residue j; for example, a proline residue may easily nucleate a helix but not propagate one; a leucine residue may nucleate and propagate a helix easily; whereas glycine may disfavor both the nucleation and propagation of a helix. Since only nearest-neighbour interactions are considered in the Zimm-Bragg model, the full partition function for a chain of N residues can be written as follows

$\mathcal{Z} = \left( 0, 1\right) \cdot \left\{ \prod_{j=1}^{N} \mathbf{W}_{j} \right\} \cdot \left( 1 , 1\right)$

where the 2x2 transfer matrix W_j of the jth residue equals the matrix of statistical weights for the state transitions

$\mathbf{W}_{j} = \begin{bmatrix} s_{j} & 1 \\ \sigma_{j} s_{j} & 1 \end{bmatrix}$

The row-column entry in the transfer matrix equals the statistical weight for making a transition from state row in residue j-1 to state column in residue j. The two states here are helix (the first) and coil (the second). Thus, the upper left entry s is the statistical weight for transitioning from helix to helix, whereas the lower left entry σs is that for transitioning from coil to helix.

[edit] See also

[edit] References

^ Samuel Kutter; Eugene M. Terentjev (16 October 2002). "Networks of helix-forming polymers". The European Physical Journal E - Soft Matter 8 (5): 539-47. PMID 15015126.
^ Ken A. Dill; Sarina Bromberg (2002). Molecular Driving Forces - Statistical Thermodynamics in Chemistry and Biology. Garland Publishing, Inc., 505.
^ Zimm, BH; Bragg JK (1959). "Theory of the Phase Transition between Helix and Random Coil in Polypeptide Chains". Journal of Chemical Physics 31: 526-531.