Charges in the hydrophobic interior of proteins

Daniel Isom, Carlos A. Castañeda, Brian R. Cannon, Priya D. Velu, Bertrand García-Moreno E

Research output: Contribution to journalArticle

123 Citations (Scopus)

Abstract

Charges are inherently incompatible with hydrophobic environments. Presumably for this reason, ionizable residues are usually excluded from the hydrophobic interior of proteins and are found instead at the surface, where they can interact with bulk water. Paradoxically, ionizable groups buried in the hydrophobic interior of proteins play essential roles, especially in biological energy transduction. To examine the unusual properties of internal ionizable groups we measured the pKa of glutamic acid residues at 25 internal positions in a stable form of staphylococcal nuclease. Two of 25 Glu residues titrated with normal pKa near 4.5; the other 23 titrated with elevated pKa values ranging from 5.2-9.4, with an average value of 7.7. Trp fluorescence and far-UV circular dichroism were used to monitor the effects of internal charges on conformation. These data demonstrate that although charges buried in proteins are indeed destabilizing, charged side chains can be buried readily in the hydrophobic core of stable proteins without the need for specialized structural adaptations to stabilize them, and without inducing any major conformational reorganization. The apparent dielectric effect experienced by the internal charges is considerably higher than the low dielectric constants of hydrophobic matter used to represent the protein interior in electrostatic continuum models of proteins. The high thermodynamic stability required for proteins to withstand the presence of buried charges suggests a pathway for the evolution of enzymes, and it underscores the need to mind thermodynamic stability in any strategy for engineering novel or altered enzymatic active sites in proteins.

Original languageEnglish (US)
Pages (from-to)16096-16100
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume107
Issue number37
DOIs
StatePublished - Sep 14 2010
Externally publishedYes

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Proteins
Thermodynamics
Micrococcal Nuclease
Protein Stability
Circular Dichroism
Static Electricity
Glutamic Acid
Catalytic Domain
Fluorescence
Water
Enzymes

Keywords

  • Bioenergetics
  • Dielectric effect
  • Electrostatics
  • Hydration
  • pKa

ASJC Scopus subject areas

  • General

Cite this

Charges in the hydrophobic interior of proteins. / Isom, Daniel; Castañeda, Carlos A.; Cannon, Brian R.; Velu, Priya D.; García-Moreno E, Bertrand.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, No. 37, 14.09.2010, p. 16096-16100.

Research output: Contribution to journalArticle

Isom, Daniel ; Castañeda, Carlos A. ; Cannon, Brian R. ; Velu, Priya D. ; García-Moreno E, Bertrand. / Charges in the hydrophobic interior of proteins. In: Proceedings of the National Academy of Sciences of the United States of America. 2010 ; Vol. 107, No. 37. pp. 16096-16100.
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