Acid pairs increase the N-terminal Ca2+ affinity of CaM by increasing the rate of Ca2+ association

被引:46
作者
Black, DJ
Tikunova, SB
Johnson, JD
Davis, JP
机构
[1] Ohio State Univ, Med Ctr, Dept Cellular & Mol Biochem, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Dept Physiol & Cell Biol, Columbus, OH 43210 USA
关键词
D O I
10.1021/bi001106+
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
A series of N-terminal calmodulin (CaM) mutants was generated to probe the relationship between the N-terminal Ca(2+) affinity and the number of paired, negatively charged Ca(2+) chelating residues in the N-terminal Ca(2+)-binding sites of CaM. When the number of acid pairs [negatively charged residues at positions +x and -x (X-axis), +y and -y (Y-axis), and +z and -z (Z-axis)] was increased from zero to one and then to two, a progressive increase was seen in the N-terminal Ca2+ affinities. The maximal ranges of the increases observed in the N-terminal Ca(2+) affinity were similar to8-8.5-fold for site I, similar to4.5-5-fold for site II, and similar to 11-fold for both sites, in comparison to the mutants containing no acid pairs. The maximal values of N-terminal Ca(2+) affinity were bestowed by the presence of five acidic chelating residues in site I or II, individually. Addition of the sixth acidic chelating residue (third acid pair) to both N-terninal Ca(2+)-binding sites reduced the N-terminal Ca(2+) affinity. The increases in Ca(2+) affinity observed were caused by an increase in the Ca(2+) association rates for the Y- and Z-axis acid pairs, while the X-axis acid pair caused a reduction in the Ca(2+) dissociation rates.
引用
收藏
页码:13831 / 13837
页数:7
相关论文
共 40 条
[1]  
BABU A, 1993, ADV EXP MED BIOL, V332, P125
[2]   The role of beta-sheet interactions in domain stability, folding, and target recognition reactions of calmodulin [J].
Browne, JP ;
Strom, M ;
Martin, SR ;
Bayley, PM .
BIOCHEMISTRY, 1997, 36 (31) :9550-9561
[3]   CALMODULIN STRUCTURE REFINED AT 1.7 ANGSTROM RESOLUTION [J].
CHATTOPADHYAYA, R ;
MEADOR, WE ;
MEANS, AR ;
QUIOCHO, FA .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 228 (04) :1177-1192
[4]   Kinetic tuning of the EF-Hand calcium binding motif: The gateway residue independently adjusts (I) barrier height and (II) equilibrium [J].
Drake, SK ;
Falke, JJ .
BIOCHEMISTRY, 1996, 35 (06) :1753-1760
[5]   MOLECULAR TUNING OF ION-BINDING TO CALCIUM SIGNALING PROTEINS [J].
FALKE, JJ ;
DRAKE, SK ;
HAZARD, AL ;
PEERSEN, OB .
QUARTERLY REVIEWS OF BIOPHYSICS, 1994, 27 (03) :219-290
[6]   The fourth EF-hand of calmodulin and its helix-loop-helix components: Impact on calcium binding and enzyme activation [J].
George, SE ;
Su, ZH ;
Fan, DJ ;
Wang, ST ;
Johnson, JD .
BIOCHEMISTRY, 1996, 35 (25) :8307-8313
[7]   Introduction of a fifth carboxylate ligand heightens the affinity of the oncomodulin CD and EF sites for Ca2+ [J].
Henzl, MT ;
Hapak, RC ;
Goodpasture, EA .
BIOCHEMISTRY, 1996, 35 (18) :5856-5869
[8]   Interconversion of the ligand arrays in the CD and EF sites of oncomodulin, influence on Ca2+-binding affinity [J].
Henzl, MT ;
Hapak, RC ;
Likos, JJ .
BIOCHEMISTRY, 1998, 37 (25) :9101-9111
[9]   Structure of the regulatory domain of scallop myosin at 2 angstrom resolution: Implications for regulation [J].
Houdusse, A ;
Cohen, C .
STRUCTURE, 1996, 4 (01) :21-32
[10]  
JOHNSON JD, 1994, J BIOL CHEM, V269, P8919