4.8 Article

Rational design of a calcium-binding protein

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 125, Issue 20, Pages 6165-6171

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja034724x

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Funding

  1. NIGMS NIH HHS [GM 62999-1, GM49871] Funding Source: Medline

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Calcium ions play key roles as structural components in biomineralization and as a second messenger in signaling pathways. We have introduced a de novo designed calcium-binding site into the framework of a non-calcium-binding protein, domain 1 of CD2. The resulting protein selectively binds calcium over magnesium with calcium-binding affinity comparable to that of natural extracellular calcium-binding proteins (K-d of 50 muM). This experiment is the first successful metalloprotein design that has a high coordination number (seven) metal-binding site constructed into a beta-sheet protein. Our results demonstrate the feasibility of designing a single calcium-binding site into a host protein, taking into account only local properties of a calcium-binding site obtained by a survey of natural calcium-binding proteins and chelators. The resulting site exhibits strong metal selectivity, suggesting that it should now be feasible to understand and manipulate signaling processes by designing novel calcium-modulated proteins with specifically desired functions and to affect their stability.

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