Multiple Evolutionary Origins of Ubiquitous Cu2+ and Zn2+ Binding in the S100 Protein Family

• Published in: PloS one Vol. 11; no. 10; p. e0164740
• Main Authors: Wheeler, Lucas C, Donor, Micah T, Prell, James S, Harms, Michael J
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 20.10.2016; Public Library of Science (PLoS)
• Subjects: Animals; Binding; Binding Sites; Biochemistry; Bioinformatics; Biological evolution; Biology and Life Sciences; Calorimetry; Chordata; Computer and Information Sciences; Copper; Copper - metabolism; DNA Mutational Analysis - methods; Evolution; Evolution, Molecular; Genomes; Humans; Metals; Models, Molecular; Molecular biology; Oikopleura; Oikopleura dioica; Origins; Phenotypes; Phylogenetics; Phylogeny; Physical sciences; Protein Binding; Protein Structure, Tertiary; Proteins; Research and Analysis Methods; S100 protein; S100 Proteins - chemistry; S100 Proteins - genetics; S100 Proteins - metabolism; Sedimentation & deposition; Signaling; Stoichiometry; Taxonomy; Titration; Titration calorimetry; Trees; Tunicata; Urochordata - metabolism; Vertebrates; Zinc; Zinc - metabolism; Oregon; United States > US
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0164740

The S100 proteins are a large family of signaling proteins that play critical roles in biology and disease. Many S100 proteins bind Zn2+, Cu2+, and/or Mn2+ as part of their biological functions; however, the evolutionary origins of binding remain obscure. One key question is whether divalent transition metal binding is ancestral, or instead arose independently on multiple lineages. To tackle this question, we combined phylogenetics with biophysical characterization of modern S100 proteins. We demonstrate an earlier origin for established S100 subfamilies than previously believed, and reveal that transition metal binding is widely distributed across the tree. Using isothermal titration calorimetry, we found that Cu2+ and Zn2+ binding are common features of the family: the full breadth of human S100 paralogs-as well as two early-branching S100 proteins found in the tunicate Oikopleura dioica-bind these metals with μM affinity and stoichiometries ranging from 1:1 to 3:1 (metal:protein). While binding is consistent across the tree, structural responses to binding are quite variable. Further, mutational analysis and structural modeling revealed that transition metal binding occurs at different sites in different S100 proteins. This is consistent with multiple origins of transition metal binding over the evolution of this protein family. Our work reveals an evolutionary pattern in which the overall phenotype of binding is a constant feature of S100 proteins, even while the site and mechanism of binding is evolutionarily labile.