Santosh A. Misal
National Institutes of Health, Brigham Young University, Savitribai Phule Pune University, Indiana University Bloomington
Research areas: Biochemistry, Genetics and Molecular Biology · Biotechnology · Advanced Proteomics Techniques and Applications · Enzyme-mediated dye degradation · Enzyme Production and Characterization
About
Dr. Santosh A. Misal is a distinguished scientist at the National Institutes of Health, Bethesda MD USA. He has a strong background in protein biochemistry, proteomics, and mass spectrometry. Dr. Misal has developed advanced techniques for single-cell proteomic analysis, particularly, single neuron analysis from healthy and ALS patients, which are crucial for precision medicine research. Dr. Misal’s work has significantly advanced the mass spectrometry and proteomics field, making him a notable figure in biomedical research.
Employment
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National Institutes of Health Staff Scientist2021 - Present
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Brigham Young University Research Associate2019 - 2021
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Indiana University Bloomington Postdoctoral Research associate2014 - 2018
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Institut de recherches cliniques de Montréal Postdoctoral research fellow2011 - 2013
Education
- 2007 - 2012
Projects & Funding
Projects & funding information is unavailable.
Publications (19)
- TDP-43-stratified single-cell proteomics of postmortem human spinal motor neurons reveals protein dynamics in amyotrophic lateral sclerosis Save
- Non-Specific Signal Peptidase Processing of Extracellular Proteins in Staphylococcus aureus N315 Save
- TDP-43-stratified single-cell proteomic profiling of postmortem human spinal motor neurons reveals protein dynamics in amyotrophic lateral sclerosis Save
- Conformational flexibility, lipid binding, and regulatory domains in CelTOS Save
- Implications of conformational flexibility, lipid binding, and regulatory domains in cell-traversal protein CelTOS for apicomplexan migration Save
- In-Depth Mass Spectrometry-Based Proteomics of Formalin-Fixed, Paraffin-Embedded Tissues with a Spatial Resolution of 50-200 μm Save
- Interpretation of anomalously long crosslinks in ribosome crosslinking reveals the ribosome interaction in stationary phase E. coli Save
- Single-Cell Proteome Profiling of Neuronal Cells Save
- Ultrasensitive single-cell proteomics workflow identifies >1000 protein groups per mammalian cell Save
- Ultrasensitive single-cell proteomics workflow identifies >1000 protein groups per mammalian cell Save
- Identification of N‐terminal protein processing sites by chemical labeling mass spectrometry Save
- Azoreductase: a key player of xenobiotic metabolism Save
- Impact of Amidination on Peptide Fragmentation and Identification in Shotgun Proteomics Save
- Enzymatic transformation of nitro-aromatic compounds by a flavin-free NADH azoreductase from Lysinibacillus sphaericus Save
- Properties of NAD (P) H Azoreductase from Alkaliphilic Red Bacteria Aquiflexum sp DL6 Save
- Purification and Characterization of Nitroreductase from Red Alkaliphilic Bacterium Aquiflexum sp DL6 Save
- Purification and characterization of nitroreductase from red alkaliphilic bacterium Aquiflexum sp. DL6. Save
- Purification and characterization of nitroreductase from red alkaliphilic bacterium Aquiflexum sp. DL6. Save
- Purification and characterization of azoreductase from alkaliphilic strain Bacillus badius Save