UDP-galactose: β-D-galactose-R 4-α-D-galac-tosyltransferase, α4Gal-T1
A novel gene defining a novel enzyme UDP-Galactose: β-D-Galactose-R 4-α-D-galactosyltransferase, termed α4Gal-T1, with unique enzymatic properties is disclosed. The invention discloses isolated DNA molecules and DNA constructs encoding α4Gal-T1 and derivatives thereof by way of amino acid deletion, substitution or insertion exhibiting α4Gal-T1 activity, as well as cloning and expression vectors including such DNA, cells transfected with vectors, and recombinant methods for providing α4Gal-T1. The enzyme α4Gal-T1 and α4Gal-active derivatives thereof are disclosed. Further, the invention discloses methods of obtaining α1, 4galactosyl glycosylated glycosphingolipids by use of an enzymatically active α4Gal-T1 protein thereof or by using cells stably transfected with a vector including DNA encoding an enzymatically active α4Gal-T1 protein as an expression system for recombinant production of such glycosphingolipids. Also a method for the identification of DNA sequence variations in the α4Gal-T1-coding exon by PCR, and detecting the presence of DNA sequence variation, are disclosed.
1. An isolated polypeptide comprising the amino acid sequence SEQ ID NO: 11.
2. An isolated polypeptide comprising an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 11 with α4Gal-T1 enzyme activity.
3. A polypeptide prepared in accordance with a method comprising:
(a) introducing into a host cell a nucleic acid encoding a polypeptide with α4Gal-T1 enzyme activity;
(b) growing the host cell under conditions suitable for expression of the polypeptide; and
(c) isolating the polypeptide produced by the host cell, wherein the polypeptide with α4Gal-T1 enzyme activity is selected from the group consisting of:
(i) a polypeptide comprising the amino acid sequence as set forth in SEQ ID No: 11;
(ii) a polypeptide comprising an amino acid sequence at least 95% identical to the amino acid sequence of SEQ ID NO: 11;
(iii) a polypeptide consisting of amino acids 46–353 of SEQ ID NO: 11; and
(iv) a fusion polypeptide consisting of at least amino acids 46–353 of SEQ ID NO: 11 fused in frame to a second polypeptide sequence.
4. A method for preparing an oligosaccharide comprising contacting a reaction mixture comprising a donor substrate and an acceptor substrate in the presence of an enzymatically active polypeptide as claimed in any of claims 1 – 3 .
5. A composition comprising the polypeptide of claim 1 and a pharmaceutically acceptable carrier, excipient or diluent.
6. A composition comprising the polypeptide of claim 2 and a pharmaceutically acceptable carrier, excipient or diluent.
7. A composition comprising the polypeptide of claim 3 and a pharmaceutically acceptable carrier, excipient or diluent.