DNA sequence analysis was performed using the BigDye Terminator v3.1 Cycle Sequencing Kit and migrated on capillary 3500 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA). Sequence similarity was performed using BLASTN [22]. Putative mutations were identified after multiple sequence alignment using Clustal W [23] and electropherogram analysis. The existence of each putative mutation was confirmed by sequencing

DNA from both parents, as well as by a secondary validation method, i.e. restriction enzyme digestion of DNA or amplification using specific primers. PCR was used additionally to confirm check details identified gene mutations (described above). Primers were designed to amplify alleles with suspected gene deletion (1318_20delAAC), by using forward primer sequences designed with (native TNAP: 5′-GCCCACAGCTCACAACAAC-3′)

or without (1318_20delAAC: 5′-GCCCACAGCTCACAACTAC-3′) the three base pair AAC deleted. PCR reactions were performed using 5 ng of DNA template, 0.4 μM each forward and reverse (5′-GTCCACGAGCAGAACTACG-3′) primers and LightCycler® FastStart DNA MasterPLUS SYBER Green I kit 1X (Roche Diagnostics, Penzberg, Germany) MG-132 price in the LightCycler® 2.0 Instrument (Roche Diagnostics). Three dimensional (3D) models of the native TNAP protein and mutants (p.N440del, p.R152C and p.N440del/p.R152C) were constructed based on the previously determined 3D structure of human placental alkaline phosphatase (PLAP) (PDB ID: 1EW2) [17] using SWISS-MODEL software (http://swissmodel.expasy.org/) [24], [25] and [26]. These models were aligned, visualized, and analyzed

using the open source software PyMOL Graphics System Molecular (Version 1.2r3pre, Schrödinger, LLC) (http://www.pymol.org). Internal contacts for native and mutant residues in the TNAP structure were analyzed using STING Millennium software [27] from the Brazilian Enterprise for Agricultural Research (EMBRAPA) (http://www.nbi.cnptia.embrapa.br/SMS/index_s.html). Atazanavir Primary dental pulp cells from both probands A and B (genotype: p.[N440del];[R152C]) and four control individuals (native TNAP) were obtained as previously reported [20]. Briefly, extracted teeth were placed in biopsy media, and pulp was harvested by cracking open the teeth using a dental chisel and hammer and removing the soft tissue with sterile forceps. Pulp cells were obtained by enzymatic digestion with 3 mg/mL collagenase type I and 4 mg/mL dispase (Gibco®, Invitrogen™, Life Technologies) for 1 h at 37 °C. Cells at passage four were seeded on coverslips in 24-well cell culture plate (2 × 104 cells per well) and were cultured in DMEM with FBS 5% for 24 h. After two washes in phosphate-buffered saline (DPBS, Invitrogen™, Life Technologies), cells were fixed in 2% paraformaldehyde in DPBS for 20 min at room temperature (RT). Blocking for non-specific binding was performed by incubating with blocking buffer solution (10% normal donkey serum in DPBS) for 45 min at RT.