The Stanford Biophysics Program is an interdisciplinary, interdepartmental predoctoral training program for students with strong backgrounds and interests in the physical sciences and their application to biology. The program draws on faculties of 16 departments in the Schools of Humanities and Sciences, Medicine, Engineering and the Stanford Synchrotron Radiation Laboratory. The program features student training and research in the application of physical and chemical principles and methods to solving biological problems, and the development of new methods. The philosophy of the training program is to develop students with strong quantitative approaches to biological problems, while also developing their perspective in choosing forefront biological problems. There are approximately 30 trainees in the program, most with undergraduate backgrounds in physical science, biochemistry, or engineering. A balanced academic program tailored to the diverse backgrounds of the students and an acceptable level of performance is insured by first year advising by the Program Director, and then annual meetings with the thesis committee. The program requires graduate-level course work in physical and biological sciences, participation in seminar series, and most importantly the development of a high level of proficiency in independent research. The major areas of modern biophysics are represented in the program, principally in the molecular basis of macromolecular function including structural biology, single molecule analysis, and computational biology. The quantitative relationship between molecular properties and higher-level cell and tissue properties, and research in emerging areas of quantitative cell and organ biology, are also well represented. Methodologies include imaging at all biological scales: single-molecule analysis; x-ray diffraction, electron microscopy, NMR and other spectroscopic methods for determining three-dimensional structure; and cellular and tissue-level MRI. Computational biophysics is also strongly represented. Outstanding facilities are available within research groups, as well as major facilities including synchrotron radiation, NMR, and laser spectroscopy.
| Fan, Chao; Fan, Minrui; Orlando, Benjamin J et al. (2018) X-ray and cryo-EM structures of the mitochondrial calcium uniporter. Nature 559:575-579 |
| Satpathy, Ansuman T; Saligrama, Naresha; Buenrostro, Jason D et al. (2018) Transcript-indexed ATAC-seq for precision immune profiling. Nat Med 24:580-590 |
| Choi, Junhong; Indrisiunaite, Gabriele; DeMirci, Hasan et al. (2018) 2'-O-methylation in mRNA disrupts tRNA decoding during translation elongation. Nat Struct Mol Biol 25:208-216 |
| McCorvy, John D; Butler, Kyle V; Kelly, Brendan et al. (2018) Structure-inspired design of ?-arrestin-biased ligands for aminergic GPCRs. Nat Chem Biol 14:126-134 |
| Choi, Junhong; Grosely, Rosslyn; Prabhakar, Arjun et al. (2018) How Messenger RNA and Nascent Chain Sequences Regulate Translation Elongation. Annu Rev Biochem 87:421-449 |
| Kaplan, Luke; Ierokomos, Athena; Chowdary, Praveen et al. (2018) Rotation of endosomes demonstrates coordination of molecular motors during axonal transport. Sci Adv 4:e1602170 |
| Latorraca, Naomi R; Wang, Jason K; Bauer, Brian et al. (2018) Molecular mechanism of GPCR-mediated arrestin activation. Nature 557:452-456 |
| Milic, Bojan; Chakraborty, Anirban; Han, Kyuho et al. (2018) KIF15 nanomechanics and kinesin inhibitors, with implications for cancer chemotherapeutics. Proc Natl Acad Sci U S A 115:E4613-E4622 |
| Knapp, Benjamin D; Huang, Kerwyn Casey (2018) Translating the Physical Code of Life. Cell 174:253-255 |
| Yang, Dian; Denny, Sarah K; Greenside, Peyton G et al. (2018) Intertumoral Heterogeneity in SCLC Is Influenced by the Cell Type of Origin. Cancer Discov 8:1316-1331 |
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