BEGIN:VCALENDAR
VERSION:2.0
PRODID:researchseminars.org
CALSCALE:GREGORIAN
X-WR-CALNAME:researchseminars.org
BEGIN:VEVENT
SUMMARY:Jakob Ruess (INRIA)
DTSTART:20250508T153000Z
DTEND:20250508T160000Z
DTSTAMP:20260421T124344Z
UID:MoRN/123
DESCRIPTION:Title: <a href="https://researchseminars.org/talk/MoRN/123/">F
 rom single cells to microbial consortia and back: stochastic chemical kine
 tics coupled to population dynamics</a>\nby Jakob Ruess (INRIA) as part of
  Seminar on the Mathematics of Reaction Networks\n\n\nAbstract\nAt the sin
 gle-cell level\, biochemical processes are inherently stochastic. Such pro
 cesses are typically studied using models based on stochastic chemical kin
 etics\, governed by a chemical master equation (CME). The CME describes th
 e time evolution of the probability distribution over system states and ha
 s been a tremendously helpful tool in shedding light on the functioning of
  cellular processes. However\, single cells are not living in isolation bu
 t are part of a growing population or community. In such contexts\, stocha
 sticity at the single-cell scale leads to population heterogeneity and cel
 ls may be subject to population processes\, such as selection\, that drive
  the population distribution away from the probability distribution of the
  single-cell process.\n\nHere\, I will introduce a multi-scale modeling fr
 amework that allows one to capture coupled stochastic single-cell and popu
 lation process. I will show that the expected population distribution of s
 uch multi-scale models can be calculated by solving a modified version of 
 the CME that is of the same dimensionality as the standard CME. I will the
 n show how such models can be used to explain experimental data on plasmid
  copy number fluctuations and population growth in media that selects agai
 nst cells that have lost the plasmid. Finally\, I will present an optogene
 tic recombination system that allows one to partition yeast populations in
 to different cell types via external application of blue light to cells an
 d show how our modeling framework can be used to predict and control emerg
 ing dynamics of the population composition in response to time-varying lig
 ht stimuli.\n
LOCATION:https://researchseminars.org/talk/MoRN/123/
END:VEVENT
END:VCALENDAR
