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. 2016 Jan 5;110(1):218–233. doi: 10.1016/j.bpj.2015.10.045

Table 1.

Values of the model parameters for influenza virus-host cell adhesion

NHA NSA K0 (mM) Veff (mM1)
3 × 50 2000 1.0 ± 0.5 × 105 2.7 ± 0.3 × 103

The parameters K0 and Veff are fitted to three experimentally measured isotherms. NHA is the number of HA monomers, and NSA is the number of SA receptors at maximum sugar loading. The number of ligands in our model is then NL = NHA, and the number of receptors NR = NSA × relative sugar loading. In principle, NHA and NSA can be treated as fitting parameters as well. The fitting problem then becomes underrestrained, however, given the small amount of isotherm data, and there are large statistical uncertainties in the fitted NHA, NSA, and K0 parameters. Instead, we used rough estimates of NHA and NSA from previous publications. It has been estimated (19) that 50 HA trimers per virus participate in forming adhesive connections, and thus NHA ≈ 3 × 50. The estimate for NSA ranges from 600 to 4500 (19, 32, 39). We used an intermediate value. Different values of NSA used in fitting result in compensatory values of Veff, but the consequent isotherms are little changed. More accurate measurements of NHA and NSA can help determine more reliably the parameters K0 and Veff. We have also fit the parameters K0 and Veff using the exact solution (Eqs. 3 and 4), obtaining the same values.