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Subtle differences in dissociation rates of interactions between destabilized human carbonic anhydrase II mutants and immobilized benzenesulfonamide inhibitors probed by a surface plasmon resonance biosensor

Svedhem, Sofia (author)
Linköpings universitet,Kemi,Tekniska högskolan
Enander, Karin (author)
Linköpings universitet,Kemi,Tekniska högskolan
Karlsson, Martin (author)
Linköpings universitet,Kemi,Tekniska högskolan
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Sjöbom, Hans (author)
Biacore AB, Uppsala, Sweden
Liedberg, Bo (author)
Linköpings universitet,Tillämpad Fysik,Tekniska högskolan
Löfås, Stefan (author)
Biacore AB, Uppsala, Sweden
Mårtensson, Lars-Göran (author)
Linköpings universitet,Kemi,Tekniska högskolan
Sjöstrand, Sven-Erik, 1938- (author)
Linköpings universitet,Cellbiologi,Hälsouniversitetet
Svensson, Stefan (author)
Linköpings universitet,Kemi,Tekniska högskolan
Carlsson, Uno (author)
Linköpings universitet,Kemi,Tekniska högskolan
Lundström, Ingemar (author)
Linköpings universitet,Tillämpad Fysik,Tekniska högskolan
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 (creator_code:org_t)
Elsevier BV, 2001
2001
English.
In: Analytical Biochemistry. - : Elsevier BV. - 0003-2697 .- 1096-0309. ; 296:2, s. 188-196
  • Journal article (peer-reviewed)
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  • The development of commercial biosensors based on surface plasmon resonance has made possible careful characterization of biomolecular interactions. Here, a set of destabilized human carbonic anhydrase II (HCA II) mutants was investigated with respect to their interaction kinetics with two different immobilized benzenesulfonamide inhibitors. Point mutations were located distantly from the active site, and the destabilization energies were up to 23 kJ/mol. The dissociation rate of wild-type HCA II, as determined from the binding to the inhibitor with higher affinity, was 0.019 s−1. For the mutants, dissociation rates were faster (0.022–0.025 s−1), and a correlation between faster dissociation and a high degree of destabilization was observed. We interpreted these results in terms of increased dynamics of the tertiary structures of the mutants. This interpretation was supported by entropy determinations, showing that the entropy of the native structure significantly increased upon destabilization of the protein molecule. Our findings demonstrate the applicability of modern biosensor technology in the study of subtle details in molecular interaction mechanisms, such as the long-range effect of point mutations on interaction kinetics.

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