Blocked lectins; methods and affinity support for making the same using affinity ligands; and method of killing selected cell populations having reduced non-selective cytotoxicity

A blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, provided that said reactive group is not a photoactivatable group, wherein said one or more affinity ligands is selected from the group consisting of affinity ligands (i) and (ii):

• ##STR3## wherein R.sub.1 is hydrogen, alkyl or aryl;
• R.sub.2 is a group inert to any subsequent reactions performed on said one or more affinity ligands or with said one or more affinity ligands present;
• L is a moiety capable of linking said ligand to a cell-binding agent;
• and wherein:
• ##STR4## =N--R.sub.1 -6-amino-6-deoxy-D-galactose .gradient.=D-galactose
• .smallcircle.=N-acetyl-D-glucosamine (2-acetamido-2-deoxy-D-glucose)
• =D-mannose, and
• --NH CO.sub.2.sup. =peptide portion of glycopeptide.

A cell-binding agent-blocked lectin conjugate comprising:

• a blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, provided that said reactive group is not a photoactivatable group;
• and
• (2) a cell-binding agent covalently linked to:
• (a) one of said covalently linked affinity ligands on the lectin via a moiety present on said affinity ligand capable of forming a covalent linkage to said cell-binding agent;
• or
• (b) said lectin via a moiety present on said lectin capable of forming a covalent linkage to a cell-binding agent, wherein said one or more .affinity ligands is selected from the group consisting of synthetic oligosaccharide analogues and synthetic glycopeptide analogues.

A cell-binding agent-blocked lectin conjugate comprising:

• (1) a blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, provided that said reactive group is not a photoactivatable group;
• and
• (2) a cell-blocking agent covalently linked to:
• (a) one of said covalently linked affinity ligands on the lectin via a moiety present on said affinity ligand capable of forming a covalent linkage to said cell-binding agent;
• or
• (b) said lectin via a moiety present on said lectin capable of forming a covalent linkage to a cell-binding agent, wherein said one or more affinity ligands is selected from the group consisting of affinity ligands (i) and (ii):
• ##STR6## wherein R.sub.1 is hydrogen, alkyl or aryl;
• R.sub.z is a group inert to any subsequent reactions performed on said one or more affinity ligands or with said one or more affinity ligands present;
• and L is a moiety capable of linking said ligand to a cell-binding agent, and wherein:
• ##STR7## =N--R.sub.1 -6-amino-6-deoxy-D-galactose .gradient.=D-galactose
• .smallcircle.=N-acetyl-D-glucosamine (2-acetamido-2-deoxy-D-glucose)
• =D-mannose, and
• --NH CO.sub.2.sup. =peptide portion of glycopeptide

A cell-binding agent-blocked lectin conjugate comprising:

• (1) a blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, provided that said reactive group is not a photoactivatable group;
• and
• (2) a cell-binding agent covalently linked to:
• (a) one of said covalently linked affinity ligands on the lectin via a moiety present on said affinity ligand capable of forming a covalent linkage to said cell-binding agent;
• or
• (b) said lectin via a moiety present on said lectin capable of forming a covalent linkage to a cell-binding agent, wherein said one or more affinity ligands comprises N-(2'-mercaptoethyl)lactamine.

A cell-binding agent-blocked lectin conjugate comprising:

• (1) a blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, provided that said reactive group is not a photoactivatable group;
• and
• (2) a cell-binding agent covalently linked to:
• (a) one of said covalently linked affinity ligands on the lectin via a moiety present on said affinity ligand capable of forming a covalent linkage to said cell-binding agent;
• or
• (b) said lectin via a moiety present on said lectin capable of forming a covalent linkage to a cell-binding agent, wherein said one or more affinity ligands comprises N-phenyllactamine.

A method of preparing a blocked lectin comprising one or more affinity ligands covalently linked by means of a reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, said method comprising the steps of:

• (1) binding at least a region of one or more activated affinity ligands having affinity for said binding sites of said lectin to said lectin;
• and
• (2) covalently linking said one or more affinity ligands to said lectin via a reactive group on said one or more affinity ligands to thereby block one or more of the binding sites of said lectin, provided that if said method is conducted with all reactants free in solution, said reactive group is not a photoactivatable group, wherein said one or more affinity ligands is selected from the group consisting of affinity ligands (i) and ##STR9## wherein R.sub.1 is hydrogen, alkyl or aryl;
• R.sub.2 is a group inert to any subsequent reactions performed on said one or more affinity ligands or with said one or more affinity ligands present;
• and L is a moiety capable of linking said ligand to a cell-binding agent, and wherein:
• ##STR10## CH.sub.2 --NH--R.sub.1 =N--R.sub.1 -6-amino-6-deoxy-D-galactose .gradient.=D-galactose
• .smallcircle.=N-acetyl-D-glucosamine (2-acetamido-2-deoxy-D-glucose)
• =D-mannose, and
• --NH CO.sub.2.sup. =peptide portion of glycopeptide.

A method of preparing a blocked lectin comprising one or more affinity ligands covalently linked by means of a first reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, wherein said blocked lectin is formed on a solid support via covalent linkage of one or more activated affinity ligands to a support, said method comprising the steps of:

• (1) making an affinity support by:
• (a) covalently linking said one or more affinity ligands to a solid support via a second reactive group present on said one or more affinity ligands;
• and
• (b) activating said one or more affinity ligands to form said first reactive group capable of covalently linking at least one of said one or more ligands to the lectin, provided that said covalent linking (a) and said activating (b) can be carried out in either order;
• (2) binding at least a region of one or more activated affinity ligands, having affinity for said binding sites of said lectin, to said lectin;
• and
• (3) covalently linking said one or more affinity ligands to said lectin via said first reactive group on said one or more affinity ligands to thereby block one or more of the binding sites of said lectin, provided that if said method is conducted with all reactants free in solution, said first reactive group is not a photoactivatable group, wherein said one or more affinity ligands comprises N-(2'-mercaptoethyl)lactamine.

A method of preparing a blocked lectin comprising one or more affinity ligands covalently linked by means of a first reactive group present on each of the ligands to a lectin such that one or more binding sites of said lectin is blocked, wherein said blocked lectin is formed on a solid support via covalent linkage of one or more activated affinity ligands to a support, said method comprising the steps of:

• (1) making an affinity support by:
• (a) covalently linking said one or more affinity ligands to a solid support via a second reactive group present on said one or more affinity ligands;
• and
• (b) activating said one or more affinity ligands to form said first reactive group capable of covalently linking at least one of said one or more ligands to the lectin, provided that said covalent linking (a) and said activating (b) can be carried out in either order;
• (2) binding at least a region of one or more activated affinity ligands, having affinity for said binding sites of said lectin, to said lectin;
• and
• (3) covalently linking said one or more affinity ligands to said lectin via said first reactive group on said one or more affinity ligands to thereby block one or more of the binding sites of said lectin, provided that if said method is conducted with all reactants free in solution, said first reactive group is not a photoactivatable group, wherein said one or more affinity ligands comprises N-phenyllactamine.