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BEGIN:VCALENDAR VERSION:2.0 PRODID:-//Penn Engineering Events - ECPv6.18.0//NONSGML v1.0//EN CALSCALE:GREGORIAN METHOD:PUBLISH X-WR-CALNAME:Penn Engineering Events X-ORIGINAL-URL:https://seasevents.nmsdev7.com X-WR-CALDESC:Events for Penn Engineering Events REFRESH-INTERVAL;VALUE=DURATION:PT1H X-Robots-Tag:noindex X-PUBLISHED-TTL:PT1H BEGIN:VTIMEZONE TZID:America/New_York BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:20180311T070000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:20181104T060000 END:STANDARD BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:20190310T070000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:20191103T060000 END:STANDARD BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:20200308T070000 END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:20201101T060000 END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTART;TZID=America/New_York:20191108T140000 DTEND;TZID=America/New_York:20191108T150000 DTSTAMP:20190923T140853Z CREATED:20190923T140853Z LAST-MODIFIED:20190923T140853Z UID:2033-1573221600-1573225200@seasevents.nmsdev7.com SUMMARY:PICS Seminar: "Mathematical Modeling of Thrombin-Fibrin Binding Dynamics" DESCRIPTION:Abstract: Blood clot formation involves the coupled processes of platelet aggregation and coagulation\, which are triggered when there is break in a blood vessel. Platelet aggregation is largely a physical process while coagulation is biochemical\, consisting of a large network of reactions that culminate in the generation of the enzyme thrombin. Thrombin cleaves fibrinogen into fibrin\, which polymerizes into fibers to form a stabilizing gel matrix in and around growing platelet aggregates. Thrombin also (re)binds directly to fibrin but this interaction\, and its purpose\, is not fully understood. Thrombin-fibrin binding is often described as two independent\, single-step binding events\, one high-affinity and one low-affinity\, each through a different exosite on thrombin. However\, kinetic schemes describing these single-step binding events with reported kinetic rate constants cannot explain experimentally-observed residency times of fibrin-bound thrombin. In this work\, we study a bivalent\, sequential-step binding scheme as an alternative to the high-affinity event\, and in addition to the low-affinity one. We developed mathematical models for the single- and sequential-step schemes consisting of reaction-diffusion equations to compare to each other and to previously published experimental data. We then used Bayesian inference\, in the form of Markov Chain Monte Carlo\, to learn model parameter distributions from the experimental data. For the model to best fit the data\, we needed an additional assumption that thrombin was irreversibly sequestered; we hypothesized that this could be due to thrombin becoming physically trapped within fibrin fibers as they formed. We also discuss how our model can be used to further probe scenarios dealing with thrombin allostery. URL:https://seasevents.nmsdev7.com/event/pics-seminar-mathematical-modeling-of-thrombin-fibrin-binding-dynamics/ LOCATION:PICS Conference Room 534 – A Wing \, 5th Floor\, 3401 Walnut Street\, Philadelphia\, PA\, 19104\, United States CATEGORIES:Colloquium ORGANIZER;CN="Penn Institute for Computational Science (PICS)":MAILTO:dkparks@seas.upenn.edu END:VEVENT END:VCALENDAR