METHODS OF POLYPEPTIDE SEQUENCING

    公开(公告)号:US20230016396A1

    公开(公告)日:2023-01-19

    申请号:US17848010

    申请日:2022-06-23

    申请人: ENCODIA, INC.

    IPC分类号: G01N33/68 G01N33/58 C12N9/48

    摘要: The present disclosure relates to methods and kits for performing an identification of a terminal amino acid residue of the polypeptide, or performing a polypeptide sequencing. The methods include a step of contacting the terminal amino acid residue of the polypeptide with a coupler, followed by attaching the coupler-polypeptide complex to the solid support and cleaving the coupler-polypeptide complex from the polypeptide, thereby isolating the terminal amino acid residue of the polypeptide from the remaining amino acid residues of the polypeptide in complex with the coupler, thereby enabling efficient identification of the terminal amino acid residue via recognition by binding agents capable of binding to the coupler-amino acid complex. In some embodiments, the coupler and the polypeptide are both associated with stabilizing components, and after binding of the coupler to the terminal amino acid of the polypeptide, tethering complex is formed between the stabilizing components releasably attached to the solid support.

    POLYPEPTIDE MODIFICATION AND CONJUGATION METHODS

    公开(公告)号:US20240000947A1

    公开(公告)日:2024-01-04

    申请号:US18201129

    申请日:2023-05-23

    申请人: Encodia, Inc.

    IPC分类号: A61K47/54

    CPC分类号: A61K47/542 A61K47/547

    摘要: The present disclosure relates to a selective and efficient method to connect a polypeptide containing at least one lysine residue to a cargo moiety, where one step of the method involves reaction of a semicarbazide group with an ortho-acylphenyl boronic acid, forming a cyclic diazaborine ring fused to phenyl. Conditions for formation of the cyclic diazaborine are sufficiently mild for the method to be used in the presence of sensitive biomolecules such as polynucleotides. A substituent group on the phenyl can be used to link the cyclic diazaborine to a cargo moiety such as a polynucleotide, bead, or reactive group, providing a polypeptide—cargo moiety conjugate that is useful for various purposes, such as to analyze, identify, track, locate, detect, or immobilize the polypeptide. Also provided are polypeptide—cargo moiety conjugates, wherein the polypeptide and cargo moiety are connected via a linker that comprises a cyclic diazaborine.

    METALLOENZYMES FOR BIOMOLECULAR RECOGNITION OF N-TERMINAL MODIFIED PEPTIDES

    公开(公告)号:US20220283175A1

    公开(公告)日:2022-09-08

    申请号:US17727677

    申请日:2022-04-22

    申请人: Encodia, Inc.

    IPC分类号: G01N33/68 G01N33/573

    摘要: The present disclosure relates to a metalloprotein binder that specifically binds to a N-terminally modified peptide. Also provided herein is a method and related kits for treating or analyzing a peptide using the metalloprotein binder and/or modified cleavase. In some embodiments, the method provided herein comprises binding metalloprotein binder-coding tag conjugates to a modified N-terminal amino acid residue of an immobilized peptide associated with a recording tag, transferring identifying information from the coding tag to the recording tag using a ligation or primer extension, and cleaving the modified N-terminal amino acid residue. The method and metalloprotein binders provided herein are useful for de novo peptide identification or sequencing.

    ARGININE MODIFICATION AND CONJUGATION METHODS

    公开(公告)号:US20230331770A1

    公开(公告)日:2023-10-19

    申请号:US18297914

    申请日:2023-04-10

    申请人: Encodia, Inc.

    IPC分类号: C07K1/107

    CPC分类号: C07K1/1077

    摘要: Provided herein are methods for modifying an arginine residue to provide a reactive handle suitable for attaching the arginine residue to a label, linker, or other target molecule. The methods utilize an Arnold Salt to convert the guanidine group of the arginine residue into a formylpyrimidine, and are efficient and very selective. Provided herein are mild reaction conditions for this arginine modification, making it suitable for use with complex biomolecules like proteins. The methods can include one or more additional steps to attach the modified arginine to a linker for further manipulation or for connecting the arginine residue to a target compound. Provided methods are especially useful for covalently linking an arginine-containing peptide to a target molecule such as a polynucleotide.