van't Hoff enthalpies without baselines

被引:91
作者
John, DM [1 ]
Weeks, KM [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
关键词
analysis of protein denaturation; differential melting curve; van't Hoff enthalpy;
D O I
10.1110/ps.9.7.1416
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Analysis of thermal melting curves represents one important approach for evaluating protein stability and the consequences of amino acid substitution on protein structure. By use of the van't Hoff relationship, the differential melting curve can be robustly fit to only three parameters, two of which are the underlying physical constants of melting temperature (T-m) and van't Hoff enthalpy (Delta H-nu H). Calculated T-m and Delta H-nu H values are insensitive to the choice of pre- and post-transition baselines. Consequently, the method accurately computes T-m and Delta H-nu H for extremely truncated data sets, in the complete absence of baseline information, and for proteins with low melting temperatures, where the traditional direct approach routinely fails. Moreover, agreement between Delta H-nu H values obtained using points derived from pre- vs. post-transition data provide an independent method for detecting some classes of non-two-state transitions. Finally, fitting of the differential denaturation curve should prove useful for analysis of abbreviated data sets obtained from high throughput array analysis of protein stability.
引用
收藏
页码:1416 / 1419
页数:4
相关论文
共 16 条
[1]   Baseline length and automated fitting of denaturation data [J].
Allen, DL ;
Pielak, GJ .
PROTEIN SCIENCE, 1998, 7 (05) :1262-1263
[2]   Thermodynamic analysis of biomolecular interactions [J].
Cooper, A .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (05) :557-563
[3]   PHAGE-T4 LYSOZYME - PHYSICAL-PROPERTIES AND REVERSIBLE UNFOLDING [J].
ELWELL, M ;
SCHELLMAN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 386 (01) :309-323
[4]   RESPONSE OF A PROTEIN-STRUCTURE TO CAVITY-CREATING MUTATIONS AND ITS RELATION TO THE HYDROPHOBIC EFFECT [J].
ERIKSSON, AE ;
BAASE, WA ;
ZHANG, XJ ;
HEINZ, DW ;
BLABER, M ;
BALDWIN, EP ;
MATTHEWS, BW .
SCIENCE, 1992, 255 (5041) :178-183
[5]  
Fersht A., 1999, STRUCTURE MECH PROTE, P508
[6]  
Freire E, 1995, METHOD ENZYMOL, V259, P144
[7]   FREE-ENERGY OF IMPERFECT NUCLEIC-ACID HELICES .3. SMALL INTERNAL LOOPS RESULTING FROM MISMATCHES [J].
GRALLA, J ;
CROTHERS, DM .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 78 (02) :301-&
[8]  
Hermans J Jr, 1965, Methods Biochem Anal, V13, P81
[9]  
HICKEY DR, 1991, J BIOL CHEM, V266, P11686
[10]   Partially formed native tertiary interactions in the A-state of cytochrome c [J].
Hostetter, DR ;
Weatherly, GT ;
Beasley, JR ;
Bortone, K ;
Cohen, DS ;
Finger, SA ;
Hardwidge, P ;
Kakouras, DS ;
Saunders, AJ ;
Trojak, SK ;
Waldner, JC ;
Pielak, GJ .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 289 (03) :639-644