Chemical event selection by suicide substrate conjugates

• US 5,571,681 A
• Filed: 03/10/1994
• Issued: 11/05/1996
• Est. Priority Date: 03/10/1994
• Status: Expired due to Fees

• Current Assignee: The Scripps Research Institute
• Original Assignee: The Scripps Research Institute
• Inventors: Janda, Kim D.
• Primary Examiner(s): Patterson, Jr., Charles L.
• Application Number:
  US08/209,525
• Time in Patent Office: 971 Days
• Field of Search: 435/188.5, 435/7.6, 435/7.71, 435/7.72, 435/41
• US Class Current: 506/10
• CPC Class Codes: C07K 16/00 Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies antibodies with enzymatic activity, e.g. abzymes C12N9/0002
• CPC Class Codes: G01N 33/56983 Viruses

Abstract

Molecules having covalent catalytic activity are identified by panning synthetic and semisynthetic combinatorial libraries on solid phase suicide substrates. In an alternative mode, mechanism-based inhibitors or affinity labels may substituted for the suicide substrate. Covalent catalysts within the combinatorial library form covalent conjugates with the suicide substrate, mechanism-based inhibitor, or affinity label. Covalent conjugates are immobilized by attachment to the suicide substrate to solid phase and are easily separated from unconjugated elements of the combinatorial library by stringent washing. Combinatorial libraries employing phagemid-display are particularly preferred since such phagemids include genetic material for identifying and amplifying conjugated catalysts. Covalent catalysts obtainable by this method include, inter alia, molecules having esterolytic activity, aldol condensation activity, β-lactamase activity, glycosidase activity, RNase activity, and proteolytic activity.

Claims

1. A method for panning a phage display protein library displaying an encoded protein having covalent catalytic activity, the method comprising the following steps:

Step A. contacting the phage display protein library with an immobilized suicide substrate for forming a covalent conjugate between the immobilized suicide substrate and the encoded protein having covalent catalytic activity;

then

Step B. separating and isolating the covalent conjugate obtained in said Step A with respect to non-covalently bound components and unbound components of the phage display protein library; and

then

Step C. decoding the encoded protein incorporated within the covalent conjugate isolated in said Step B for identifying the encoded protein having covalent catalytic activity.

2. A method for panning an encoded protein library for an encoded protein having covalent catalytic activity as described in claim 1 wherein the catalytic activity is selected from the group consisting of esterolytic activity, aldol condensation activity, β

-lactamase activity, glycosidase activity, RNase activity, and proteolytic activity.

3. A chemical complex comprising:

a solid phase,

a suicide substrate covalently linked to said solid phase,

a catalytically active protein covalently linked to said suicide substrate for forming a covalent protein/suicide substrate conjugate, said catalytically active protein, when not covalently linked to said suicide substrate, having a covalent catalytic activity wherein,

the catalytically active protein is displayed on a phage having a nucleotide sequence encoding the catalytically active protein displayed thereon,

whereby said phage is immobilized on the solid phase via said catalytically active protein.

4. A method for catalytically converting a substrate to a product, the method comprising the following steps:

Step A;

providing a catalytic protein having a covalent catalytic activity with respect to both the substrate and an immobilized suicide substrate according to the following substeps;

Substep 1;

contacting a phage display protein library with the immobilized suicide substrate, said contacting resulting in the formation of a covalent conjugate between the immobilized suicide substrate and the catalytic protein;

then

Substep 2;

separating and isolating the covalent conjugate obtained in said Substep 1 with respect to noncovalently bound components and unbound components of the phage display protein library;

then

Substep 3;

decoding the catalytic protein incorporated within the covalent conjugate isolated in said Substep 2;

then

Substep 4;

producing the catalytic protein identified in said Substep 3; and

then

Step B;

contacting the catalytic protein of said Step A with the substrate under reaction conditions for producing the product.

5. A method for catalytically converting a substrate to a product as described in claim 4 wherein the catalytic activity of the catalytic protein is selected from the group consisting of esterolytic activity, aldol condensation activity, β

-lactamase activity, glycosidase activity, RNase activity, and proteolytic activity.