Methods and reagents for analyzing protein-protein interfaces
AssigneeRevolution Medicines, Inc.
InventorsGregory L. Verdine, M. James Nichols, Sharon A. Townson, Uddhav Kumar Shigdel, Seung-Joo Lee, Dylan T. Stiles, Neville J. Anthony
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Abstract
The present disclosure provides methods and reagents useful for analyzing protein-protein interfaces such as interfaces between a presenter protein (e.g., a member of the FKBP family, a member of the cyclophilin family, or PIN1) and a target protein. In some embodiments, the target and/or presenter proteins are intracellular proteins. In some embodiments, the target and/or presenter proteins are mammalian proteins.
Claims4
A compound, or salt thereof, which binds to cyclophilin and which has the structure:
- A-L-B,
- wherein A is a cyclophilin binding moiety having the structure of Formula III:
- wherein Z3 and Z4 are each, independently, hydroxyl, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 heteroalkyl, or Z3 and Z4 combine to form, with the atoms to which they are attached, an optionally substituted 13 to 40 member macrocycle;
- Z4 comprises a point of attachment to L;
- R5 is optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl, optionally substituted C2-C6 alkynyl, optionally substituted C1-C6 heteroalkyl, optionally substituted C2-C6 heteroalkenyl, optionally substituted C2-C6 heteroalkynyl, optionally substituted C3-C10 carbocyclyl, optionally substituted C6-C10 optionally substituted C6-C10 aryl C1-C6 alkyl, optionally substituted C2-C9 heterocyclyl, or optionally substituted C2-C9 heterocyclyl C1-C6 alkyl;
- R6 is optionally substituted C1-C6 alkyl;
- L is a linker having the structure:
- A1-(B1)f—(C1)g—(B2)h-(D)-(B3)i—(C2)j—(B4)k-A2
- wherein A1 is a bond between the linker and A;
- A2 is a bond between B and the linker;
- B1, B2, B3, and B4 each, independently, is selected from optionally substituted C1-C2 alkyl, optionally substituted C1-C3 heteroalkyl, O, S, and NRN;
- RN is hydrogen, optionally substituted C1-4 alkyl, optionally substituted C2-4 alkenyl, optionally substituted C2-4 alkynyl, optionally substituted C2-6 heterocyclyl, optionally substituted C6-12 aryl, or optionally substituted C1-7 heteroalkyl;
- C1 and C2 are each, independently, selected from carbonyl, thiocarbonyl, sulphonyl, or phosphoryl;
- f, g, h, l, j, and k are each, independently, 0 or 1;
- and D is optionally substituted C1-10 alkyl, optionally substituted C2-10 alkenyl, optionally substituted C2-10 alkynyl, optionally substituted C2-6 heterocyclyl, optionally substituted C6-12 aryl, optionally substituted C2-C10 polyethylene glycol, or optionally substituted C1-10 heteroalkyl, or a chemical bond linking A1-(B1)f—(C1)g—(B2)h— to —(B3)i—(C2)j—(B4)k-A2;
- and
- B is a cross-linking group, wherein the cross-linking group is a maleimide, vinyl sulfone having the structure
- isocyanate, isothiocyanate, or haloheteroaryl.
Dependencies are inferred from the claim text.