say The MATCHMAKER Two-Hybrid System was used following the manufacturer’s recommended protocol. The two-hybrid pGADT7-Rec vector containing the sequences for glvps or Dglvps were used as bait, while acph and m1 genes were inserted into the pGBKT7 vector, yielding the pGlVpsAD, pGlVps-YQII -AD, pAcPh-BD, and pm1-BD vectors, respectively. The vectors pLRP-HA and pm1-BD were used as control. The AH109 transformants were cultured at 30uC for 4 5 days on plates with minimal medium lacking leucine and tryptophan to test for positive transformation, or in the absence of leucine, tryptophan, and histidine to study specific protein interactions as previously described. High-stringency medium that also lacked adenine was also used to test strong MedChemExpress AG-1478 protein-protein interactions. Controls included the pESCP-AD/pm1-BD interaction or pGlLRP-AD/pm2-BD and the pGlVps-AD/ pGBKT7 or pGADT7/ pGlVpsBD vector. Results The subcellular localization of the soluble hydrolase AcPh Giardia Hydrolase Receptor observed between AcPh-V5/H6 transgenic and wild-type trophozoites in these assays. Detailed AcPh-V5/H6 localization was obtained using immunoelectron microscopy of transgenic trophozoites. An illustrative electron micrograph of a Giardia trophozoite was shown to better describe the PVs and BZ . Labeling with anti-V5 mAb and the gold-labeled secondary antibody showed a distinctive signal, consistent with the localization of AcPh in these organelles. No labeling was observed in treated wild-type trophozoites. 
Altogether, these results suggested that, after synthesis in the ER, AcPh was delivered to the acidic compartment where it became active. Identification of the acid phosphatase receptor The awareness that the soluble lysosomal protein AcPh might require a receptor-mediated sorting process, prompted PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22211113 us to initiate a search for a candidate using AcPh as bait. This result encouraged the use of AcPh-V5/H6 transgenic trophozoites to purify AcPh together with its associated proteins by pull-down assay. AcPh-V5/H6 was purified from transgenic cells using agarose-immobilized nickel ions that bound the string of histidine residues of AcPh. Linked proteins were eluted, analyzed by SDSPAGE, and submitted to the Research Technologies Branch for Protein Identification for LC-MS/MS analysis. After three independent experiments, three proteins associated with AcPh were identified. Besides the identification of two protein bands corresponding to the AcPh, BLAST search and sequence analysis identified proteins involved in protein trafficking, including a sequence encoding to the kinesin-like protein, the Vacuolar protein sorting 35, and a sequence corresponding to an hypothetical protein. Analysis of homologous sequences of GL50803_28954 using the different predictive programs did not provide information about the possible function of this protein. However, analysis of the protein sequences of 550 amino acids showed that this protein contained a lysosomal tyrosine-based motif YQII at its C-terminus, suggesting that it might be the receptor involved in binding and transport of AcPh to PVs in Giardia. Analysis of its expression by RT-PCR showed that GL50803_28954 was expressed in growing trophozoites. Because at that time the corresponding gene sequence was deprecated from the GDB, we decided to corroborate the start codon of the protein sequence by designing a set of primers that amplified a fragment of 1490 bp and another pair to amplify the whole predicted 1653 bp ORF. Thes
