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PRODID:-//Biomedical Mathematics Group - ECPv6.16.5.1//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Biomedical Mathematics Group
X-ORIGINAL-URL:https://www.ibs.re.kr/bimag
X-WR-CALDESC:Events for Biomedical Mathematics Group
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BEGIN:VTIMEZONE
TZID:Asia/Seoul
BEGIN:STANDARD
TZOFFSETFROM:+0900
TZOFFSETTO:+0900
TZNAME:KST
DTSTART:20190101T000000
END:STANDARD
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BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20201224T130000
DTEND;TZID=Asia/Seoul:20201224T140000
DTSTAMP:20210406T075331Z
CREATED:20210223T094304Z
LAST-MODIFIED:20210406T075331Z
UID:3983-1608814800-1608818400@www.ibs.re.kr
SUMMARY:Seokjoo Chae\, Ligand-receptor promiscuity enables cellular addressing
DESCRIPTION:We will discuss about “Ligand-receptor promiscuity enables cellular addressing”\, Su et al.\, bioRxiv (2021) \nIn multicellular organisms\, secreted ligands selectively activate\, or “address\,” specific target cell populations to control cell fate decision-making and other processes. Key cell-cell communication pathways use multiple promiscuously interacting ligands and receptors\, provoking the question of how addressing specificity can emerge from molecular promiscuity. To investigate this issue\, we developed a general mathematical modeling framework based on the bone morphogenetic protein (BMP) pathway architecture. We find that promiscuously interacting ligand-receptor systems allow a small number of ligands\, acting in combinations\, to address a larger number of individual cell types\, each defined by its receptor expression profile. Promiscuous systems outperform seemingly more specific one-to-one signaling architectures in addressing capacity. Combinatorial addressing extends to groups of cell types\, is robust to receptor expression noise\, grows more powerful with increasing receptor multiplicity\, and is maximized by specific biochemical parameter relationships. Together\, these results identify fundamental design principles governing cell addressing by ligand combinations.
URL:https://www.ibs.re.kr/bimag/event/2020-12-24_1/
LOCATION:KAIST E2-1 room 3221\, E2-1 building\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Journal Club,Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
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