Show simple item record

dc.contributor.authorRichards, DM
dc.contributor.authorEndres, RG
dc.date.accessioned2016-05-23T09:43:05Z
dc.date.issued2016-05-16
dc.description.abstractPhagocytosis and receptor-mediated endocytosis are vitally important particle uptake mechanisms in many cell types, ranging from single-cell organisms to immune cells. In both processes, engulfment by the cell depends critically on both particle shape and orientation. However, most previous theoretical work has focused only on spherical particles and hence disregards the wide-ranging particle shapes occurring in nature, such as those of bacteria. Here, by implementing a simple model in one and two dimensions, we compare and contrast receptor-mediated endocytosis and phagocytosis for a range of biologically relevant shapes, including spheres, ellipsoids, capped cylinders, and hourglasses. We find a whole range of different engulfment behaviors with some ellipsoids engulfing faster than spheres, and that phagocytosis is able to engulf a greater range of target shapes than other types of endocytosis. Further, the 2D model can explain why some nonspherical particles engulf fastest (not at all) when presented to the membrane tip-first (lying flat). Our work reveals how some bacteria may avoid being internalized simply because of their shape, and suggests shapes for optimal drug delivery.en_GB
dc.description.sponsorshipDMR and RGE were supported by BBSRC grant BB/I019987/1. DMR was also supported by the Wellcome Trust Institutional Strategic Support Award (WT105618MA). RGE also acknowledges funding from ERC Starting Grant 280492-PPHPI.en_GB
dc.identifier.doi10.1073/pnas.1521974113
dc.identifier.urihttp://hdl.handle.net/10871/21651
dc.language.isoenen_GB
dc.publisherNational Academy of Sciencesen_GB
dc.subjectendocytosisen_GB
dc.subjectphagocytosisen_GB
dc.subjectshape dependenceen_GB
dc.subjectStefan problemen_GB
dc.titleTarget shape dependence in a simple model of receptor-mediated endocytosis and phagocytosisen_GB
dc.typeArticleen_GB
dc.date.available2016-05-23T09:43:05Z
dc.identifier.issn1091-6490
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.en_GB
dc.identifier.journalProceedings of the National Academy of Sciencesen_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record