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. Author manuscript; available in PMC: 2008 Nov 20.
Published in final edited form as: Biochemistry. 2007 Oct 24;46(46):13415–13424. doi: 10.1021/bi700774s

Table 2. Ca2+association and dissociation rate constants for native and mutant CaMs free in solution or bound to BSCaMIQ.

Ca2+ binding was modeled according to a sequential mechanism with a rapidly equilibrating first step (Scheme 1), so these rate constants correspond with the second Ca2+-binding step. Values indicated by an “NA” are not applicable; those indicated by an “ND” are too fast to measure in the stopped-flow fluorometer, which has a dead-time of ~1.4 ms. Association rate constants (kon) designated by a superscript “A” were calculated using the dissociation rate constants (koff ) given in this table and previously determined equilibrium constants for the second Ca2+ binding step (15). Association rate constants for the C-ter EF hand pair in the CaM-BSCaMIQ complex were derived from a global analysis of the fluorescence time courses presented in Fig. 5. koff values designated by a superscript “B” were determined using a 5 µl observation cell, which reduces the stopped-flow dead time to below 1 ms, but unfortunately cannot be used with solutions containing BSCaMIQ due to their higher viscosity. koff values for the CaM-BSCaMIQ complex given in parenthesis were derived from a global analysis the fluorescence time courses presented in Fig. 4. All other koff values were derived from quin-2 fluorescence data (Fig. 3).

N-ter EF hand pair C-ter EF hand pair
CaM kon (M−1s−1) koff (s−1) kon (M−1s−1) koff (s−1)
NC 3.1±1.2×108 A 1152±117B 3.4±2.4×107 A 10.3±0.7
NxC NA NA 5.8±3.2×107 A 10.8±0.6
NCx 3.4±1.5×108 A 1298±135B NA NA
CaM-BSCaMIQ kon (M−1s−1) koff (s−1) kon (M−1s−1) koff(s−1)
NC 3.0±1.2×108 A 473.4±37.9
(528.3±3.3)
3.2±0.1×106 11.7±0.5
(13.5±0.1)
NxC NA NA 3.1±0.1×106 11.8±0.5
NCx ND ND NA NA