Postdoctoral scientist with a great passion to work on Drug development.Skilled in drug screening, assay development, protein biochemistry, and structural biology,
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Healthcare StrategistC-FactorBerlin, De -
Co-Founder And CroOnuBerlin, De -
Postdoctoral ScientistMax Delbrück Center Feb 2023 - PresentBerlin, GermanyI am continuing my scientific work from my Ph.D. on developing these molecules further. Looking forward to #collaborations and #funding opportunities in this field. -
Doctoral ResearcherMax Delbrück Center Mar 2017 - Jan 2023Berlin Area, GermanyDrug Screening for the Dynamin super-family of proteinsWorked on a drug development project, where I am looking for molecule(s) that would modulate the activity of my target protein. This change in activity would further downstream regulate cellular pathways in membrane trafficking. I first established a kinase assay in the presence of lipids that could be taken to high-throughput screening (HTS). Validated the outcomes of HTS in different assay setups.Two of the validated… Show more Drug Screening for the Dynamin super-family of proteinsWorked on a drug development project, where I am looking for molecule(s) that would modulate the activity of my target protein. This change in activity would further downstream regulate cellular pathways in membrane trafficking. I first established a kinase assay in the presence of lipids that could be taken to high-throughput screening (HTS). Validated the outcomes of HTS in different assay setups.Two of the validated hits showed a specific cellular response in cell-based assays, the rest compounds showed non-specific cellular effects and were eliminated from further studies. These are the first reported inhibitors against my target protein. The potential therapeutic importance of the two compounds could be in the treatment of obesity and breast cancer. In my initial first two years of my Ph.D., I was working on different projects.One of them was, Structural organization of Septin scaffoldsIn this study, we showed that Septin1 was necessary for the structural and functional integrity of Golgi apparatus. Show less -
Research AssociateNanyang Technological University May 2015 - Feb 2017SingaporeMechanism of chaperone function of prostaglandin synthase (L-PGDS) for amyloid beta-peptides (Aβ)Solved the crystal structure of L-PGDS (PDB - 5WY9)Optimized the expression and purification of Aβ40 peptide. Did thioflavin assay to test chaperonin activity against amyloidogenic peptides. Biomolecular interaction was measured using surface plasmon resonance and Isothermal titration calorimetry.Electron microscopy (TEM) to see amyloid fibril formation and their inhibition… Show more Mechanism of chaperone function of prostaglandin synthase (L-PGDS) for amyloid beta-peptides (Aβ)Solved the crystal structure of L-PGDS (PDB - 5WY9)Optimized the expression and purification of Aβ40 peptide. Did thioflavin assay to test chaperonin activity against amyloidogenic peptides. Biomolecular interaction was measured using surface plasmon resonance and Isothermal titration calorimetry.Electron microscopy (TEM) to see amyloid fibril formation and their inhibition in presence of L-PGDSSet up crystallization trials of L-PGDS with Aβ40 and ligands (Heme and Retinoic acid)NMR on Bruker Avance II 600 MHz spectrometer to see protein-RNA interaction Show less -
Sipga StudentA*Star - Agency For Science, Technology And Research Jul 2013 - Oct 2014SingaporeStructural and Functional studies of PRDM family of proteins (lysine methytransferases).In this project we cloned, expressed and purified PRDM members 9,14 and 15. Set up crystallization trials of the protein in its apo-form and along with its substrate.Studied binding property of Cellular nucleic acid binding protein (CNBP) with RNA and ssDNA bybiochemical assays.Methods: Protein expression, protein purification, protein crystallization, electrophoretic mobilty shift… Show more Structural and Functional studies of PRDM family of proteins (lysine methytransferases).In this project we cloned, expressed and purified PRDM members 9,14 and 15. Set up crystallization trials of the protein in its apo-form and along with its substrate.Studied binding property of Cellular nucleic acid binding protein (CNBP) with RNA and ssDNA bybiochemical assays.Methods: Protein expression, protein purification, protein crystallization, electrophoretic mobilty shift assay. Show less -
Dissertation ThesisIndian Institute Of Technology, Bombay 2012 - 2013Mumbai Area, IndiaPurification and crystallization of histo aspartic protease (HAP) and to determine high resolution crystal structure from Plasmodium Falciparum.In this project I extensively optimized the protocol of expression and purification of HAP protein.Set up crystallization trials manually (hanging drop). -
Summer Research InternInstitut Curie - Hopital René Huguenin May 2012 - Jul 2012Paris Area, FranceRole of posttranslational modification of tubulin in CancerCell culture (Hela, RPE1 and U2OS cell lines).RNA extraction from cell followed by PCR analysis.Protein extraction from cell followed by immunoblot analysis as well as immunofluorescence analysis
Saif Mohd. Skills
Saif Mohd. Education Details
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Doctor Of Philosophy - Phd -
Bioengineering And Biomedical Engineering -
Biotechnology
Frequently Asked Questions about Saif Mohd.
What company does Saif Mohd. work for?
Saif Mohd. works for C-Factor
What is Saif Mohd.'s role at the current company?
Saif Mohd.'s current role is Healthcare Strategist.
What schools did Saif Mohd. attend?
Saif Mohd. attended Freie Universität Berlin, Indian Institute Of Technology, Bombay, Jamia Millia Islamia.
What skills is Saif Mohd. known for?
Saif Mohd. has skills like Protein Purification, Bioinformatics, Cell Culture, Western Blotting, Spectroscopy, Crystallography, Immunofluorescence, Pcr, Immunoblotting.
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