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The ALS5 gene of Candida albicans and analysis of the Als5p N‐terminal domain
Author(s) -
Hoyer L. L.,
Hecht J. E.
Publication year - 2001
Publication title -
yeast
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.923
H-Index - 102
eISSN - 1097-0061
pISSN - 0749-503X
DOI - 10.1002/1097-0061(200101)18:1<49::aid-yea646>3.0.co;2-m
Subject(s) - biology , candida albicans , corpus albicans , gene , genetics , antiparallel (mathematics) , pichia pastoris , sequence analysis , serine , peptide sequence , microbiology and biotechnology , recombinant dna , physics , quantum mechanics , magnetic field , phosphorylation
ALS genes of Candida albicans encode a family of cell‐surface glycoproteins with a three‐domain structure. Each Als protein has a relatively conserved N‐terminal domain, a central domain consisting of a tandemly repeated motif, and a serine‐threonine‐rich C‐terminal domain that is relatively variable across the family. The ALS family exhibits several types of variability that indicate the importance of considering strain and allelic differences when studying ALS genes and their encoded proteins. Analysis of ALS5 provided additional evidence of variability within the ALS family. Comparison of the ALS5 sequence from two strains indicated sequence differences larger than strain or allelic mismatches observed for other C. albicans genes. Screening a collection of commonly used C. albicans strains and clinical isolates indicated that ALS5 is not present in several of these strains, supporting the conclusion that the Als protein profile is variable among C. albicans isolates. Physical mapping of ALS5 showed that it is located close to ALS1 on chromosome 6. The N‐terminal domain of Als5p was produced in Pichia pastoris to initiate structural analysis of this portion of the protein. The hydrophobic character of this portion of the protein was exploited in the purification scheme. Circular dichroism analysis of the purified, authenticated protein yielded a high content of antiparallel β‐sheet and little to no α‐helical structure. These results are consistent with the conclusion that the N‐terminal domain of Als5p has an immunoglobulin fold structure similar to that found in many cell adhesion molecules. Gene sequences of C. albicans ALS5 (Accession No. AF068866) and TPI1 (Accession No. AF124845) have been deposited in the GenBank database. Copyright © 2000 John Wiley & Sons, Ltd.