dc.contributor.author | Goguen, Brenda N. | |
dc.contributor.author | Imperiali, Barbara | |
dc.date.accessioned | 2012-11-27T18:23:29Z | |
dc.date.available | 2012-11-27T18:23:29Z | |
dc.date.issued | 2011-10 | |
dc.date.submitted | 2011-08 | |
dc.identifier.issn | 1554-8929 | |
dc.identifier.issn | 1554-8937 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/75036 | |
dc.description.abstract | Cell migration is required for many physiological processes, including wound repair and embryogenesis, and relies on precisely orchestrated events that are regulated in a spatially and temporally controlled manner. Most traditional approaches for studying migration, such as genetic methods or the use of chemical inhibitors, do not offer insight into these important components of protein function. However, chemical tools, which respond on a more rapid time scale and in localized regions of the cell, are capable of providing more detailed, real-time information. This Review describes these recent approaches to investigate cell migration and focuses on proteins that are activated by light or small molecules, as well as fluorescent sensors of protein activity. | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.). Cell Migration Consortium (Grant GM064346) | en_US |
dc.description.sponsorship | National Institute of General Medical Sciences (U.S.) (Biotechnology Training Grant T32-GM08334) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society (ACS) | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/cb200299k | en_US |
dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
dc.source | Prof. Imperiali via Erja Kajosalo | en_US |
dc.title | Chemical Tools for Studying Directed Cell Migration | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Goguen, Brenda N., and Barbara Imperiali. “Chemical Tools for Studying Directed Cell Migration.” ACS Chemical Biology 6.11 (2011): 1164–1174. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.approver | Imperiali, Barbara | |
dc.contributor.mitauthor | Goguen, Brenda N. | |
dc.contributor.mitauthor | Imperiali, Barbara | |
dc.relation.journal | ACS Chemical Biology | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Goguen, Brenda N.; Imperiali, Barbara | en |
dc.identifier.orcid | https://orcid.org/0000-0002-5749-7869 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |