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Structural and kinetic analysis of Schistosoma mansoni Adenylosuccinate Lyase ( Sm ADSL)

DOI: 10.1016/j.molbiopara.2017.03.006 DOI Help

Authors: Larissa Romanello (Universidade de São Paulo) , Vitor Hugo Balasco Serrao (Universidade de São Paulo) , Juliana Roberta Torini De Souza (Universidade de São Paulo) , Louise E. Bird (OPPF-UK; Wellcome Trust Centre for Human Genetics, University of Oxford) , Joanne E. Nettleship (OPPF-UK; Wellcome Trust Centre for Human Genetics, University of Oxford) , Heather Rada (OPPF-UK; Wellcome Trust Centre for Human Genetics, University of Oxford) , Yamini Reddivari (OPPF-UK; Wellcome Trust Centre for Human Genetics, University of Oxford) , Ray J. Owens (OPPF-UK; Wellcome Trust Centre for Human Genetics, University of Oxford) , Ricardo De Marco (Universidade de São Paulo) , Jose Brandao-neto (Diamond Light Source) , Humberto D' Muniz Pereira (Universidade de São Paulo)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Molecular And Biochemical Parasitology

State: Published (Approved)
Published: March 2017
Diamond Proposal Number(s): 5073 , 5894

Abstract: Schistosoma mansoni is the parasite responsible for schistosomiasis, a disease that affects about 218 million people worldwide. Currently, both direct treatment and disease control initiatives rely on chemotherapy using a single drug, praziquantel. Concerns over the possibility of resistance developing to praziquantel, have stimulated efforts to develop new drugs for the treatment of schistosomiasis. Schistosomes do not have the de novo purine biosynthetic pathway, and instead depend entirely on the purine salvage pathway to supply its need for purines. The purine salvage pathway has been reported as a potential target for developing new drugs against schistosomiasis. Adenylosuccinate lyase (SmADSL) is an enzyme in this pathway, which cleaves adenylosuccinate (ADS) into adenosine 5'-monophosphate (AMP) and fumarate. SmADSL kinetic characterization was performed by isothermal titration calorimetry (ITC) using both ADS and SAICAR as substrates. Structures of SmADSL in Apo form and in complex with AMP were elucidated by x-ray crystallography revealing a highly conserved tetrameric structure required for their function since the active sites is formed from residues of three different subunits. The active sites are also highly conserved between species and it is difficult to identify a potent species-specific inhibitor for the development of new therapeutic agents. In contrast, several mutagenesis studies have demonstrated the importance of dimeric interface residues in the stability of the quaternary structure of the enzyme. The lower conservation of these residues between SmADSL and human ADSL could be used to lead the development of anti-schistosomiasis drugs based on disruption of subunit interfaces. These structures and kinetics data add another layer of information to Schistosoma mansoni purine salvage pathway.

Journal Keywords: Schistosoma mansoni; purine salvage pathway; adenylosuccinate lyase

Subject Areas: Biology and Bio-materials, Medicine


Instruments: I02-Macromolecular Crystallography