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. Author manuscript; available in PMC: 2014 Mar 21.
Published in final edited form as: J Phys Chem B. 2013 Mar 12;117(11):3098–3109. doi: 10.1021/jp311936j

Table 3.

LRAP layer protein coverage and hydration obtained by assuming protein SLD values. The protein SLDs were calculated assuming 0% or 100% deuteration of LRAP by exchange of labile protons with D2O solvent (Table S2).

Model %D exchange Layer Protein SLD × 106−2) LRAP coverage (v%) Hydration (v%) gH2O/g protein1
One layer protein 0 2.16 70.2±0.04 29.8±0.4 0.32
100 3.13 74.1±1.2 20.7±0.5 0.21
Two layer monomer-inner high protein SLD2 0 Inner 2.31 65.5±1.2 32.0±0.6 0.37
Outer 1.81 80.5±5.0 18.7±1.4 0.17
100 Inner 3.82 63.5±1.7 25.0±1.1 0.29
Outer 2.55 73.6±1.6 13.1±0.9 0.13
Two layer monomer-inner low protein SLD3 0 Inner 1.81 30.24±22.5 60±18 1.49
Outer 2.31 66.3±3.4 29.5±3.1 0.33
100 Inner 2.55 74.65±1.31 25.2±0.94 0.26
Outer 3.82 89.22±1.63 10.6±1.2 0.09
1

Degree of hydration calculated in terms of grams of water (H2O) per grams of protein.

2

Protein SLDs were calculated assuming the inner layer was the C-terminus (42–59) and inner N-terminus (8–24) and the outer layer was the outer N-terminus (1–7) and middle hydrophobic region (25–41) as described in the text and supplementary section.

3

Protein SLDs were calculated assuming the protein was flipped - inner layer was the N-terminus (1–7) and middle hydrophobic region (25–41) and the outer layer was the C-terminus (42–59) and inner N-terminus (8–24).