Alanine-scanning mutagenesis of WH2 domains of VopF reveals residues important for conferring lethality in a Saccharomyces cerevisiae model.
DIR@IMTECH: CSIR-Institute of Microbial Technology
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Title |
Alanine-scanning mutagenesis of WH2 domains of VopF reveals residues important for conferring lethality in a Saccharomyces cerevisiae model.
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Creator |
Tripathi, Ranjana
Kaithwas, Vikas Dureja, Chetna Raychaudhuri, Saumya |
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Subject |
QR Microbiology
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Description |
VopF, the type III effector molecule, has been implicated in the pathogenesis of non-O1, non-O139 strains of Vibrio cholerae. It is a protein of 530 amino acids, comprises of one formin homology 1-like (FH1-like) domain and three WASP homology 2 (WH2) domains. Previous works have demonstrated that WH2 domains are crucial for VopF function as a modulator of cellular actin homeostasis. Furthermore, domain deletion analysis also suggests that VopF variant constituted with only WH2 domain 3 is more efficient in restricting the growth of budding yeast than its congeners containing either only domain 1 or domain 2. Interestingly, a good degree of sequence diversity is present within each WH2 domain of VopF. In order to ascertain the importance of different amino acids in each WH2 domain, a systemic alanine scanning mutagenesis was employed. Using a yeast model system, the alanine derivatives of each amino acid of WH2 domain 1 and 3 of VopF were examined for growth restricting activity. Taken together, our mutagenesis results reveal the identification of critical residues of WH2 domain 1 and 3 of VopF.
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Publisher |
Elsevier Science Ltd
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Date |
2013-08-01
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Type |
Article
PeerReviewed |
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Relation |
https://www.sciencedirect.com/science/article/pii/S0378111913005684?via%3Dihub
http://crdd.osdd.net/open/2118/ |
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Identifier |
Tripathi, Ranjana and Kaithwas, Vikas and Dureja, Chetna and Raychaudhuri, Saumya (2013) Alanine-scanning mutagenesis of WH2 domains of VopF reveals residues important for conferring lethality in a Saccharomyces cerevisiae model. Gene, 525 (1). pp. 116-23. ISSN 1879-0038
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