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Updated: Jun 12, 2026

Immuno-fluorescence Assay of Leptospiral Surface-exposed Proteins
Published on: July 1, 2011
Complement regulator-acquiring surface protein 1 of Borrelia burgdorferi binds to human bone morphogenic protein 2,
Teresia Hallström1, Katrin Haupt, Peter Kraiczy
1Department of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, Jena, Germany.
Insights
Borrelia burgdorferi
Area of Science:
- Microbiology
- Infectious Diseases
- Molecular Biology
Background:
- Borrelia burgdorferi, the agent of Lyme disease, possesses complement regulator-acquiring surface proteins (CRASPs).
- CRASP-1 is one such protein, but its specific role in infection requires further elucidation.
Purpose of the Study:
- To identify novel human proteins that bind to CRASP-1.
- To understand the functional implications of CRASP-1 interactions with host proteins.
Main Methods:
- Protein-protein interaction studies to identify CRASP-1 binding partners.
- Mapping of plasminogen-binding regions on CRASP-1.
- Enzymatic assays to assess plasminogen activation and activity.
Main Results:
- Identified several novel human CRASP-1 binding proteins, including extracellular matrix components (collagen I, III, IV, fibronectin, laminin) and plasminogen.
- Localized plasminogen-binding sites to two distinct regions of CRASP-1.
- Demonstrated that CRASP-1-bound plasminogen can be activated to plasmin by urokinase-type plasminogen activator, yielding active plasmin capable of cleaving fibrinogen.
Conclusions:
- CRASP-1 is a multifunctional protein involved in host-pathogen interactions.
- CRASP-1 binds to extracellular matrix proteins and plasminogen, potentially facilitating bacterial adhesion, colonization, and dissemination.
- These interactions may play a significant role in the pathogenesis and organ tropism of Borrelia burgdorferi infections.
Abstract:
Lyme disease-causing Borrelia burgdorferi spirochetes express up to 5 complement regulator-acquiring surface proteins (CRASPs). To better define how CRASP-1 contributes to infection, we aimed to identify novel CRASP-1-binding host proteins. Here, we identified a number of novel human CRASP-1-binding proteins, including bone morphogenic protein 2, collagen I, collagen III, collagen IV, fibronectin, laminin, and plasminogen. The plasminogen-binding regions were located in 2 separate regions of CRASP-1. Our results demonstrated that plasminogen-bound CRASP-1 can be converted to plasmin by the urokinase-type plasminogen activator and that proteolytically active plasmin cleaves the synthetic chromogenic substrate S-2251 and the natural substrate fibrinogen. In conclusion, CRASP-1 is a multifunctional protein of B. burgdorferi that binds to several human extracellular matrix proteins and plasminogen. These interactions may contribute to adhesion, bacterial colonization, and organ tropism and may allow dissemination of B. burgdorferi in the host.
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