pH, Indicators, Equilibrium, and Buffer Solutions

Author(s):  
Frank Brescia ◽  
John Arents ◽  
Herbert Meislich ◽  
Amos Turk ◽  
Eugene Weiner
Author(s):  
R. Y. Tsien ◽  
A. Minta ◽  
M. Poenie ◽  
J.P.Y. Kao ◽  
A. Harootunian

Recent technical advances now enable the continuous imaging of important ionic signals inside individual living cells with micron spatial resolution and subsecond time resolution. This methodology relies on the molecular engineering of indicator dyes whose fluorescence is strong and highly sensitive to ions such as Ca2+, H+, or Na+, or Mg2+. The Ca2+ indicators, exemplified by fura-2 and indo-1, derive their high affinity (Kd near 200 nM) and selectivity for Ca2+ to a versatile tetracarboxylate binding site3 modeled on and isosteric with the well known chelator EGTA. The most commonly used pH indicators are fluorescein dyes (such as BCECF) modified to adjust their pKa's and improve their retention inside cells. Na+ indicators are crown ethers with cavity sizes chosen to select Na+ over K+: Mg2+ indicators use tricarboxylate binding sites truncated from those of the Ca2+ chelators, resulting in a more compact arrangement of carboxylates to suit the smaller ion.


1996 ◽  
Vol 61 (11) ◽  
pp. 1600-1608
Author(s):  
Mohamed E. Ahmed

The interfacial behaviour and adsorption equilibria of mono-, di-, and triphosphate of inosine (IMP, IDP, and ITP) were carried out in different buffer solutions by phase-sensitive ac voltammetry at HMDE. The characteristic properties and adsorption parameters of dilute and compact layers were evaluated from the obtained Frumkin isotherm at different pH values. The effect of some divalent metal ions on the adsorption stage and association of the investigated compounds has been studied.


Author(s):  
Dennis Sherwood ◽  
Paul Dalby

Many reactions in solution involve acids and bases, and so this chapter examines these important reactions in detail. Topics covered include the ionisation of water, pH, pOH, acids and bases, conjugate acids and conjugate bases, acid and base dissociation constants, the Henderson-Hasselbalch equation, the Henderson-Hasselbalch approximation, buffer solutions and buffer capacity. A unique feature of this chapter is a ‘first principles’ analysis of how a reaction buffered at a particular pH achieves an equilibrium composition different from that of the same reaction taking place in an unbuffered solution. This introduces some concepts which are important in understanding the biochemical standard state, as required for Chapter 23.


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