Calcium Regulates the Activity and Structural Stability of Tpr, a Bacterial Calpain-like Peptidase

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

DOI

  • Dominika Staniec, Poland
  • Miroslaw Ksiazek, Poland
  • Ida B Thøgersen
  • Jan J Enghild
  • Aneta Sroka, Poland
  • Danuta Bryzek, Poland
  • Matthew Bogyo, United States
  • Magnus Abrahamson, United States
  • Jan Potempa, Poland

Porphyromonas gingivalis is a peptide-fermenting asaccharolytic periodontal pathogen. Its genome contains several genes encoding cysteine peptidases other than gingipains. One of these genes (PG1055) encodes a protein called Tpr (thiol protease), which has sequence similarity to cysteine peptidases of the papain and calpain families. In this study, we biochemically characterize Tpr. We found that the 55 kDa Tpr inactive zymogen proteolytically processes itself into active forms of 48 kDa, 37 kDa, and 33 kDa via sequential truncations at the N-terminus. These processed molecular forms of Tpr are associated with the bacterial outer membrane, where they are likely responsible for the generation of metabolic peptides required for survival of the pathogen. Both autoprocessing and activity were dependent on calcium concentrations greater than 1 mM, consistent with the protein's activity within the intestinal and inflammatory milieus. Calcium also stabilized the Tpr structure and rendered the protein fully resistant to proteolytic degradation by gingipains. Together, our findings suggest that Tpr is an example of a bacterial calpain, a calcium-responsive peptidase that may generate substrates required for the peptide-fermenting metabolism of P. gingivalis. Aside from nutrient generation, Tpr may also be involved in evasion of host immune response through degradation of the antimicrobial peptide LL-37 and complement proteins C3, C4 and C5. Taken together, these results indicate that Tpr likely represents an important pathogenesis factor for P. gingivalis.

Original languageEnglish
JournalJournal of Biological Chemistry
Volume290
Pages (from-to)27248-27260
Number of pages13
ISSN0021-9258
DOIs
Publication statusPublished - 6 Nov 2015

See relations at Aarhus University Citationformats

ID: 93271009