Thermodynamic and kinetic analysis of porphyrin binding to Trichosanthes cucumerina seed lectin

Kenoth, Roopa ; Reddy, D. Raghunath ; Maiya, Bhaskar G. ; Swamy, Musti J. (2001) Thermodynamic and kinetic analysis of porphyrin binding to Trichosanthes cucumerina seed lectin European Journal of Biochemistry, 268 (21). pp. 5541-5549. ISSN 0014-2956

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Official URL: http://onlinelibrary.wiley.com/doi/10.1046/j.1432-...

Related URL: http://dx.doi.org/10.1046/j.1432-1033.2001.02491.x

Abstract

The interaction of several metallo-porphyrins with the galactose-specific lectin from Trichosanthes cucumeirna (TCSL) has been investigated. Difference absorption spectroscopy revealed that significant changes occur in the Soret band region of the porphyrins upon binding to TCSL and these changes have been monitored to obtain association constants (Ka) and stoichiometry of binding (n). The dimeric lectin binds two porphyrin molecules and the presence of the specific saccharide lactose did not affect porphyrin binding significantly, indicating that the sugar and the porphyrin bind at different sites. The Ka values obtained for the binding of different porphyrins with TCSL at 25 °C were in the range of 2 × 103-5 × 105 m-1. Association constants for meso-tetra(4-sulphonatophenyl)porphyrinato copper(II) (CuTPPS), a porphyrin bearing four negative charges and meso-tetra(4-methylpyridinium)porphyrinato copper(II) (CuTMPyP), a porphyrin with four positive charges, were determined at several temperatures; from the temperature dependence of the association constants, the thermodynamic parameters change in enthalpy (Δ H) and change in entropy (Δ S) associated with the binding process were estimated. The thermodynamic data indicate that porphyrin binding to TCSL is driven largely by a favourable entropic contribution; the enthalpic contribution is very small, suggesting that the binding process is governed primarily by hydrophobic forces. Stopped-flow spectroscopic measurements show that binding of CuTMPyP to TCSL takes place by a single-step process and at 20 °C, the association and dissociation rate constants were 1.89 × 104 m-1·s-1 and 0.29 s-1, respectively.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Haemagglutinin; Photodynamic Therapy; Stopped-flow Spectroscopy
ID Code:32165
Deposited On:31 Mar 2011 10:01
Last Modified:17 May 2016 14:57

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