Modified chitin-binding domain and use thereof
View Patent ↗Compositions and methods are provided for reversibly binding chitin binding domain (CBD) to a chitin or equivalent substrate under non denaturing conditions. CBD is modified preferably by a mutation to achieve this change in properties. In one embodiment, an aromatic amino acid residue located in the binding cleft of the CBD was altered resulting in reversible binding affinity for substrate in select conditions. Creating a modified CBD with an altered binding affinity for substrate provides new uses for CBD not previously possible with unmodified CBD which binds irreversibly to chitin.
1. A method of obtaining a chitin binding domain (CBD) capable of reversibly binding to a chitin substrate under non-denaturing conditions, wherein the non-denaturing conditions are selected from the group consisting of non-denaturing ionic conditions, non-denaturing pH, and non-denaturing detergent concentration, the method comprising:
(a) modifying at least one amino acid within the CBD;
(b) selecting the modified CBD according to its binding to the chitin substrate; and
(c) determining whether the modified CBD is capable of reversibly binding chitin under non-denaturing conditions.
2. A method according to claim 1 , wherein modifying at least one amino acid within the CBD, further comprises:
mutating a portion of a DNA sequence encoding the CBD and expressing the DNA in a host cell or by in vitro translation.
3. A method according to claim 2 , wherein mutating a portion of the DNA sequence, further comprises:
substituting a portion of the DNA sequence encoding the CBD with an oligonucleotide, the oligonucleotide differing from an unmodified CBD by a mutation at a target site within the CBD.
4. A method according to claim 3 , wherein the target site is a tryptophan and the mutation is a phenylalanine substitution of the tryptophan.
5. A method according to claim 1 , wherein the selected non-denaturing conditions comprises a reduction in NaCl molarity from a salt concentration of 2M NaCl to a salt concentration in the range of 0–1M NaCl.