To understand relationships between protein sequence and stability, we often compare data from proteins that differ by the substitution of one amino acid. Frequently, an amino acid change causes the cooperative denaturation transitions to shift to lower temperatures, diminishing the signal from the native state. Here we show that apparent stability changes, i.e., the free energy of denaturation, Delta G(D), can also be caused by a deficiency of points in the low temperature end of the transition. In addition, we suggest a method for overcoming this problem.
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Virginia Mil Inst, Dept Mech Engn, 710 Nichols Hall, Lexington, VA 24450 USAVirginia Mil Inst, Dept Mech Engn, 710 Nichols Hall, Lexington, VA 24450 USA
Bruns, Morgan C.
Leventon, Isaac T.
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NIST, Fire Res Div, Gaithersburg, MD 20899 USAVirginia Mil Inst, Dept Mech Engn, 710 Nichols Hall, Lexington, VA 24450 USA
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Australian Natl Univ, Res Sch Phys, Dept Elect Mat Engn, Canberra, ACT 2601, AustraliaAustralian Natl Univ, Res Sch Phys, Dept Elect Mat Engn, Canberra, ACT 2601, Australia
Bandara, Y. M. Nuwan D. Y.
Saharia, Jugal
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Southern Methodist Univ, Dept Mech Engn, Dallas, TX 75275 USAAustralian Natl Univ, Res Sch Phys, Dept Elect Mat Engn, Canberra, ACT 2601, Australia
Saharia, Jugal
Karawdeniya, Buddini, I
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Australian Natl Univ, Res Sch Phys, Dept Elect Mat Engn, Canberra, ACT 2601, AustraliaAustralian Natl Univ, Res Sch Phys, Dept Elect Mat Engn, Canberra, ACT 2601, Australia