The Protein Chemistry Laboratory Core will serve as the major protein preparation and analysisresource for the Program Project. The laboratory will be responsible for protein preparation,characterization and identification which will include hypothesis and project driven proteomics. TheProtein Chemistry Laboratory is equipped with three automated peptide synthesizers, an automatedEdman sequencer, various HPLC and FPLC systems encompassing both micro and macro scale.Most importantly the laboratory has two 'proteomics-appropriate' mass spectrometry systemsequipped with ionization modes that will enable sub-picomole analysis of proteins and peptides withbio-informatics support. All protein and peptide products will be subjected to stringentcharacterization by mass spectrometric/ proteomic analysis. Surface Plasmon resonance (Biacore)analysis is also available that is adaptable to coupling with the on-site mass spectrometers.The primary services provided will be the provision of protein-related tools and reagents such aspurified murine complement system proteins, monoclonal and polyclonal antibodies, syntheticpeptides, and peptide-like synthetic antagonists that interrupt various and specific complementsystem protein-protein interactions. Hypothesis driven proteomics will also be applied to delineatemolecular and biochemical mechanisms underlying the various complement regulated diseasemodels. All members of the program project will be served by the PCLC.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI068730-02
Application #
7686427
Study Section
Special Emphasis Panel (ZAI1-QV-I (M1))
Project Start
2008-09-01
Project End
2012-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
2
Fiscal Year
2008
Total Cost
$248,446
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Chen, Lan-Sun; Kourtzelis, Ioannis; Singh, Rashim Pal et al. (2018) Endothelial Cell-Specific Overexpression of Del-1 Drives Expansion of Haematopoietic Progenitor Cells in the Bone Marrow. Thromb Haemost :
Lamont, Richard J; Koo, Hyun; Hajishengallis, George (2018) The oral microbiota: dynamic communities and host interactions. Nat Rev Microbiol 16:745-759
Bostanci, Nagihan; Bao, Kai; Li, Xiaofei et al. (2018) Gingival Exudatome Dynamics Implicate Inhibition of the Alternative Complement Pathway in the Protective Action of the C3 Inhibitor Cp40 in Nonhuman Primate Periodontitis. J Proteome Res 17:3153-3175
Ricklin, Daniel; Mastellos, Dimitrios C; Reis, Edimara S et al. (2018) The renaissance of complement therapeutics. Nat Rev Nephrol 14:26-47
Kwak, Jeff W; Laskowski, Jennifer; Li, Howard Y et al. (2018) Complement Activation via a C3a Receptor Pathway Alters CD4+ T Lymphocytes and Mediates Lung Cancer Progression. Cancer Res 78:143-156
Mastellos, Dimitrios C; Reis, Edimara S; Yancopoulou, Despina et al. (2018) Expanding Complement Therapeutics for the Treatment of Paroxysmal Nocturnal Hemoglobinuria. Semin Hematol 55:167-175
Reis, Edimara S; Mastellos, Dimitrios C; Ricklin, Daniel et al. (2018) Complement in cancer: untangling an intricate relationship. Nat Rev Immunol 18:5-18
Sauter, Reinhard J; Sauter, Manuela; Reis, Edimara S et al. (2018) Functional Relevance of the Anaphylatoxin Receptor C3aR for Platelet Function and Arterial Thrombus Formation Marks an Intersection Point Between Innate Immunity and Thrombosis. Circulation 138:1720-1735
Reis, Edimara S; Berger, Nadja; Wang, Xin et al. (2018) Safety profile after prolonged C3 inhibition. Clin Immunol 197:96-106
Laabei, Maisem; Liu, Guanghui; Ermert, David et al. (2018) Short Leucine-Rich Proteoglycans Modulate Complement Activity and Increase Killing of the Respiratory Pathogen Moraxella catarrhalis. J Immunol 201:2721-2730

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