The serpin superfamily is a large group of medium-size proteins (approximately 45 60kDa) that have a common three-dimensional fold that represents a metastable conformation of the protein. Despite the common tertiary fold, inhibition of serine or cysteine proteinases, blood transport of thyroid hormones, blood generation of the vasoactive hormone angiotensin, neurite-outgrowth-promoting-ability, regulation of tumor invasion, involvement in cellular differentiation and regulation of apoptosis. The long term goal of this program project is to understand the metastable folding pathway and consequences of the metastable serpin fold both for normal and pathological function, and in conferring the particular properties of a given serpin, whether the (anti-thrombin, alpha1-proteinase inhibitor, and crmA), (ii) is able to undergo conformational change but without the ability to inhibit proteinase (thyroxine binding globulin) or (iii) acts neither as an inhibitor nor appears to undergo the serpin conformational change (angiotensin). The present proposal represents a concerted attach on some of the most important outstanding questions on serpin structure and function. The program comprises four projects that address different aspects of this goal. Studies include those on the structure of the nature of the inhibition mechanism of both serine and cysteine proteinases and how serpins are able to kinetically trap complexes with proteinase (Project 2, Steven Olson, P.I.), why the serpin fold should still be needed for the non- inhibitory serpins angiotensinogen and thyroxine binding globulin (Project 3, Phillip Patston, P.I.), and the x-ray structures of serpins and their complexes with proteinases and specific ligands (Project 4, Karl Volz, P.I.). There are three cores consisting of an administrative core, a molecular biology and cell culture core, and a protein expression and purification core. All three cores will be used by all four projects. The project represents an inter-departmental and inter-college collaboration, involving investigators in four departments and two colleges of the University of Illinois at Chicago as well as a group of internationally- recognized collaborating investigators.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL064013-04
Application #
6625296
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Program Officer
Link, Rebecca P
Project Start
2000-02-22
Project End
2004-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
4
Fiscal Year
2003
Total Cost
$1,094,233
Indirect Cost
Name
University of Illinois at Chicago
Department
Biochemistry
Type
Schools of Medicine
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612
Duhan, U; Patston, P (2010) Explanation for the high heat stability of thyroxine binding globulin-Chicago. Endocr Regul 44:43-7
Swanson, Richard; Raghavendra, Manikanahally P; Zhang, Weiqing et al. (2007) Serine and cysteine proteases are translocated to similar extents upon formation of covalent complexes with serpins. Fluorescence perturbation and fluorescence resonance energy transfer mapping of the protease binding site in CrmA complexes with granzyme J Biol Chem 282:2305-13
Dementiev, Alexey; Dobo, Jozsef; Gettins, Peter G W (2006) Active site distortion is sufficient for proteinase inhibition by serpins: structure of the covalent complex of alpha1-proteinase inhibitor with porcine pancreatic elastase. J Biol Chem 281:3452-7
Tesch, Lisa D; Raghavendra, Manikanahally P; Bedsted-Faarvang, Tina et al. (2005) Specificity and reactive loop length requirements for crmA inhibition of serine proteases. Protein Sci 14:533-42
Simonovic, Miljan; Denault, Jean-Bernard; Salvesen, Guy S et al. (2005) Lack of involvement of strand s1'A of the viral serpin CrmA in anti-apoptotic or caspase-inhibitory functions. Arch Biochem Biophys 440:1-9
Gettins, Peter G W; Backovic, Marija; Peterson, Francis C (2004) Use of NMR to study serpin function. Methods 32:120-9
Al-Ayyoubi, Maher; Gettins, Peter G W; Volz, Karl (2004) Crystal structure of human maspin, a serpin with antitumor properties: reactive center loop of maspin is exposed but constrained. J Biol Chem 279:55540-4
Dementiev, Alexey; Petitou, Maurice; Herbert, Jean-Marc et al. (2004) The ternary complex of antithrombin-anhydrothrombin-heparin reveals the basis of inhibitor specificity. Nat Struct Mol Biol 11:863-7
Patston, Philip A; Church, Frank C; Olson, Steven T (2004) Serpin-ligand interactions. Methods 32:93-109
O'Keeffe, Denis; Olson, Steven T; Gasiunas, Nijole et al. (2004) The heparin binding properties of heparin cofactor II suggest an antithrombin-like activation mechanism. J Biol Chem 279:50267-73

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