PXD011826 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Identification and characterization of Acanthamoeba cyst wall proteins |
Description | Acanthamoeba castellanii, cause of keratitis and blindness, is an emerging pathogen because of its association with contact lens use. The cyst wall contributes to pathogenesis as cysts are resistant to sterilizing reagents in lens solutions and to antibiotics applied to the eye. Here we used structured illumination microscopy (SIM) and probes for sugar polymers to show that purified cyst walls of A. castellanii retain endocyst and ectocyst layers and conical structures (ostioles) that connect them. Mass spectrometry showed candidate cyst wall proteins (CWPs) are dominated by three families of lectins (named here Luke, Leo, and Jonah), because each binds to microcrystalline cellulose +/- chitin. Luke lectins contain two or three carbohydrate-binding modules (CBM49), which were first identified in a tomato cellulase. Leo lectins have two unique domains with eight cysteines each (8-Cys) +/- a Thr-, Lys-, and His-rich spacer. Jonah lectins contain one or three choice-of-anchor A (CAA) domains previously of unknown function. Representative members of each family were tagged with green fluorescent protein (GFP) and expressed under their own promoters in transfected parasites. A representative Jonah lectin with one CAA domain is made early during encystation and localizes to the ectocyst layer. In contrast, Leo and Luke lectins are made later and localize to the endocyst layer and ostioles. Probes for CWPs (anti-GFP antibodies) and for sugar polymers (maltose-binding protein-fusions with CWPs) suggest Jonah lectin and sugar polymers to which it binds are accessible in the ectocyst layer, while Luke and Leo lectins and sugar polymers to which they bind are mostly inaccessible in the ectocyst layer and ostioles. In summary, these results show the most abundant A. castellanii CWPs are three sets of lectins, which localize to either the ectocyst layer (Jonah) or endocyst layer and ostioles (Luke and Leo). |
HostingRepository | PRIDE |
AnnounceDate | 2019-05-21 |
AnnouncementXML | Submission_2019-05-21_05:32:17.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD011826 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Angelo Lopez |
SpeciesList | scientific name: Acanthamoeba castellanii str. Neff; NCBI TaxID: 1257118; |
ModificationList | Deamidated; Oxidation; Carbamidomethyl; Gln->pyro-Glu |
Instrument | Q Exactive HF; Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2018-11-26 02:44:36 | ID requested | |
⏵ 1 | 2019-05-21 05:32:18 | announced | |
Publication List
Magistrado-Coxen P, Aqeel Y, Lopez A, Haserick JR, Urbanowicz BR, Costello CE, Samuelson J, The most abundant cyst wall proteins of Acanthamoeba castellanii are lectins that bind cellulose and localize to distinct structures in developing and mature cyst walls. PLoS Negl Trop Dis, 13(5):e0007352(2019) [pubmed] |
Keyword List
curator keyword: Biological |
submitter keyword: Acanthamoeba, lectins, cyst wall proteins |
Contact List
John Crawford Samuelson |
contact affiliation | Dept. of Molecular & Cell Biology, Boston University, Boston, Massachusetts |
contact email | jsamuels@bu.edu |
lab head | |
Angelo Lopez |
contact affiliation | BU |
contact email | lopezangelo1991@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD011826
- Label: PRIDE project
- Name: Identification and characterization of Acanthamoeba cyst wall proteins