Show simple item record

dc.contributor.authorRajapaksha, Maheshinie
dc.contributor.authorLovell, Scott
dc.contributor.authorJanowiak, Blythe E.
dc.contributor.authorAndra, Kiran K.
dc.contributor.authorBattaile, Kevin P.
dc.contributor.authorBann, James G.
dc.date.accessioned2013-07-10T16:25:56Z
dc.date.available2013-07-10T16:25:56Z
dc.date.issued2012-10
dc.identifier.citationRajapaksha, Maheshinie; Lovell, Scott; Janowiak, Blythe E.; Andra, Kiran K.; Battaile, Kevin P.; Bann, James G. 2012. pH effects on binding between the anthrax protective antigen and the host cellular receptor CMG2. Protein Science, v.21 no.10 pp.1467-1480en_US
dc.identifier.issn0961-8368
dc.identifier.otherWOS:000308994300006
dc.identifier.urihttp://dx.doi.org/10.1002/pro.2136
dc.identifier.urihttp://hdl.handle.net/10057/5903
dc.descriptionClick on the DOI link to access the article (may not be free).en_US
dc.description.abstractThe anthrax protective antigen (PA) binds to the host cellular receptor capillary morphogenesis protein 2 (CMG2) with high affinity. To gain a better understanding of how pH may affect binding to the receptor, we have investigated the kinetics of binding as a function of pH to the full-length monomeric PA and to two variants: a 2-fluorohistidine-labeled PA (2-FHisPA), which is 1 pH unit more stable to variations in pH than WT, and an 1 pH unit less stable variant in which Trp346 in the domain 2 beta 3-2 beta 4 loop is substituted with a Phe (W346F). We show using stopped-flow fluorescence that the binding rate increases as the pH is lowered for all proteins, with little influence on the rate of dissociation. In addition, we have crystallized PA and the two variants and examine the influence of pH on structure. In contrast to previous X-ray studies, the domain 2 beta 3-2 beta 4 loop undergoes little change in structure from pH 8 to 5.5 for the WT protein, but for the 2-FHis labeled and W346F mutant there are changes in structure consistent with previous X-ray studies. In accord with pH stability studies, we find that the average B-factor values increase by 2030% for all three proteins at low pH. Our results suggest that for the full-length PA, low pH increases the binding affinity, likely through a change in structure that favors a more bound-like conformation.en_US
dc.language.isoen_USen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofseriesProtein Science;v.21 no.10
dc.titlepH effects on binding between the anthrax protective antigen and the host cellular receptor CMG2en_US
dc.typeArticleen_US


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record