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SUMMARY:Structural analysis and conformational dynamics of the SARS-CoV-2 r
 eplication–transcription complex
LOCATION:Virtual
TZID:America/Denver
DTSTART:20211104T160000
UID:2026-04-30-16-23-35@natsci.colostate.edu
DTSTAMP:20260430T162335
Description:About the Seminar:\n\nThe SARS-CoV-2 genome is replicated and t
 ranscribed by its RNA-dependent RNA polymerase\, nsp12\, along with severa
 l accessary cofactors\, together known as the replication–transcription 
 complex.  Helicase nsp13 is one of the cofactors that is essential for vi
 ral replication.  Structural analyses of the SARS-CoV-2 replication–tra
 nscription complex revealed that nsp12 stably binds to two copies of nsp13
 \, but the role of the two nsp13 molecules as well as how they are coupled
  to the polymerase during viral genome replication are less clear.  In th
 is presentation\, I will talk about how a combination of cryo-electron mic
 roscopy and molecular dynamics simulation provided evidence of an unexpect
 ed allosteric regulatory mechanism that couples the helicase and polymeras
 e during SARS-CoV-2 genome replication.\n\n&nbsp\;\n\nAbout the Speaker:\n
 \nQi Wang holds a B.S. in physical chemistry from Peking University and a
  Ph.D. in biophysics from Cornell University. After he completed his postd
 octoral training in the laboratory of John Kuriyan at U.C. Berkeley\, Qi W
 ang joined D.E. Shaw Research as a research scientist. Qi’s research int
 erests include studying structure and function of enzymes on membranes\, a
 llosteric regulation of protein by small molecules and RNA/DNA remodeling 
 by protein complexes.\n\n&nbsp\;\n\nJoin Zoom Meeting\nhttps://zoom.us/j/9
 4537157545?pwd=b1NuYkRNcCtGK1A3OWxITWVmTm0xdz09\n\nMeeting ID: 945 3715 75
 45\nPasscode: 635287\n\nJoin by SIP\n94537157545@zoomcrc.com\n\n&nbsp\; 4:
 00 pm
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