Collection and methods for its use

US10647757B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10647757-B2
Application numberUS-201715449561-A
CountryUS
Kind codeB2
Filing dateMar 3, 2017
Priority dateMay 29, 2009
Publication dateMay 12, 2020
Grant dateMay 12, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present disclosure enables methods of identifying the VH and VL class pairs in the human immune repertoire, determining the VH and VL class pairs that are most prevalent and those having favorable biophysical properties. More specifically, the collections of the present disclosure comprise the most prevalent and/or preferred VH and VL class pairings with highly diversified CDRs.

First claim

Opening claim text (preview).

We claim: 1. A collection of synthetic antibody fragments comprising variable heavy chain and variable light chain framework regions, wherein said synthetic antibody fragments are selected from Fab, F(ab′)2, Fab′, Fv, scFv, single chains which include an Fc portion and nanobodies, wherein said framework regions comprise germline protein sequences, wherein said germline protein sequences comprise the following properties: i) four or less post translational modifications in the complementarity determining regions; ii) two or less methionines in the complementarity determining regions; iii) one or less unpaired cysteines; iv) one or less T-cell epitopes; and v) an isoelectric point of at least 7.5; and wherein said collection of synthetic antibody fragments comprises germline protein sequences of at least two different germline protein pairs, wherein the germline protein pairs are selected from IGHV1-18 (SEQ ID NO: 65)/IGKV1-05 (SEQ ID NO: 118); IGHV1-18 (SEQ ID NO: 65)/IGLV2-23 (SEQ ID NO: 174); IGHV1-46 (SEQ ID NO: 68)/IGKV1-09 (SEQ ID NO: 121); IGHV1-46 (SEQ ID NO:68)/IGKV1-39 (SEQ ID NO: 129); IGHV1-46 (SEQ ID NO: 68)/IGKV3-15 (SEQ ID NO:153); IGHV1-69*01 (SEQ ID NO: 70)/IGKV1-05 (SEQ ID NO: 118); IGHV3-07 (SEQ ID NO: 77)/IGKV1-09 (SEQ ID NO: 121); IGHV3-07 (SEQ ID NO: 77)/IGKV1-12 (SEQ ID NO: 122); IGHV3-07 (SEQ ID NO: 77)/IGKV1-27 (SEQ ID NO: 126); IGHV3-07 (SEQ ID NO: 77)/IGKV3-15 (SEQ ID NO: 153); IGHV3-07 (SEQ ID NO: 77)/IGLV1-47 (SEQ ID NO: 167); IGHV3-07 (SEQ ID NO: 77)/IGLV2-23 (SEQ ID NO: 174); IGHV3-07 (SEQ ID NO: 77)/IGLV3-01 (SEQ ID NO: 175); IGHV3-11 (SEQ ID NO: 79)/IGKV1-05 (SEQ ID NO: 118); IGHV3-11 (SEQ ID NO: 79)/IGKV1-06 (SEQ ID NO: 119); IGHV3-11 (SEQ ID NO: 79)/IGKV1-12 (SEQ ID NO: 122); IGHV3-11 (SEQ ID NO: 79)/IGKV1-16 (SEQ ID NO: 124); IGHV3-11 (SEQ ID NO: 79)/IGKV3-15 (SEQ ID NO: 153); IGHV3-11 (SEQ ID NO: 79)/IGLV1-47 (SEQ ID NO: 167); IGHV3-11 (SEQ ID NO: 79)/IGLV2-23 (SEQ ID NO: 174); IGHV3-15 (SEQ ID NO: 81)/IGKV1-05 (SEQ ID NO: 118); IGHV3-15 (SEQ ID NO: 81)/IGKV1-06 (SEQ ID NO: 119); IGHV3-15 (SEQ ID NO: 81)/IGKV1-09 (SEQ ID NO: 121); IGHV3-15 (SEQ ID NO: 81)/IGKV1-12 (SEQ ID NO: 122); IGHV3-15 (SEQ ID NO: 81)/IGKV1-16 (SEQ ID NO: 124); IGHV3-15 (SEQ ID NO: 81)/IGKV1-27 (SEQ ID NO: 126); IGHV3-15 (SEQ ID NO: 81)/IGKV1-39 (SEQ ID NO: 129); IGHV3-15 (SEQ ID NO: 81)/IGKV3-15 (SEQ ID NO: 153); IGHV3-15 (SEQ ID NO: 81)/IGLV1-40 (SEQ ID NO: 165); IGHV3-15 (SEQ ID NO: 81)/IGLV1-51 (SEQ ID NO: 169); IGHV3-15 (SEQ ID NO: 81)/IGLV2-11 (SEQ ID NO: 171); IGHV3-21 (SEQ ID NO: 84)/IGKV1-06 (SEQ ID NO: 119); IGHV3-21 (SEQ ID NO: 84)/IGKV1-12 (SEQ ID NO: 122); IGHV3-21 (SEQ ID NO: 84)/IGKV1-27 (SEQ ID NO: 126); IGHV3-21 (SEQ ID NO: 84)/IGKV1-39 (SEQ ID NO: 129); IGHV3-21 (SEQ ID NO: 84)/IGLV2-14 (SEQ ID NO: 172); IGHV3-21 (SEQ ID NO: 84)/IGLV2-23 (SEQ ID NO: 174); IGHV3-30 (SEQ ID NO: 86)/IGLV2-23 (SEQ ID NO: 174); IGHV3-30 (SEQ ID NO: 86)/IGLV3-1 (SEQ ID NO: 175); IGHV3-33 (SEQ ID NO: 89)/IGKV3-15 (SEQ ID NO: 153); IGHV3-33 (SEQ ID NO: 89)/IGLV2-23 (SEQ ID NO: 174); IGHV3-48 (SEQ ID NO: 93)/IGKV1-27 (SEQ ID NO: 126); IGHV3-53 (SEQ ID NO: 95)/IGKV1-09 (SEQ ID NO: 121); IGHV3-53 (SEQ ID NO: 95)/IGKV1-12 (SEQ ID NO: 122); IGHV3-53 (SEQ ID NO: 95)/IGLV1-51 (SEQ ID NO: 169); IGHV3-53 (SEQ ID NO: 95)/IGLV2-23 (SEQ ID NO: 174); IGHV3-53 (SEQ ID NO: 95)/IGLV3-1 (SEQ ID NO: 175); IGHV3-74 (SEQ ID NO: 100)/IGKV1-06 (SEQ ID NO: 119); IGHV3-74 (SEQ ID NO: 100)/IGKV1-09 (SEQ ID NO: 121); IGHV3-74 (SEQ ID NO: 100)/IGKV1-27 (SEQ ID NO: 126); IGHV3-74 (SEO ID NO: 100)/IGKV3-15 (SEQ ID NO: 153); IGHV3-74 (SEQ ID NO: 100)/IGLV1-51 (SEQ ID NO: 169); IGHV4-04 (SEQ ID NO: 102)/IGLV2-23 (SEQ ID NO: 174); IGHV4-04 (SEQ ID NO: 102)/IGLV3-1 (SEQ ID NO: 175); IGHV4-04 (SEQ ID NO: 102)/IGLV3-21 (SEQ ID NO: 182); IGHV4-39 (SEQ ID NO: 109)/IGLV2-14 (SEQ ID NO: 172); IGHV4-39 (SEQ ID NO: 109)/IGLV3-1 (SEQ ID NO: 175); IGHV5-51 (SEQ ID NO:113)/IGKV1-09 (SEQ ID NO: 121); IGHV5-51 (SEQ ID NO: 113)/IGLV2-23 (SEQ ID NO: 174); IGHV5-51 (SEQ ID NO: 113)/IGLV3-1 (SEQ ID NO: 175); IGHV6-1 (SEQ ID NO:115)/IGKV1-06 (SEQ ID NO: 119); and IGHV6-1 (SEQ ID NO: 115)/IGLV2-23 (SEQ ID NO: 174). 2. The collection according to claim 1 , wherein said collection of synthetic antibody fragments comprises at least five different variable heavy chain germline protein sequences. 3. The collection according to claim 1 , wherein said synthetic antibody fragments comprise human sequences. 4. The collection according to claim 1 , wherein said synthetic antibody fragments comprise one or more complementarity determining regions comprising germline protein sequences. 5. The collection according to claim 1 , where said synthetic antibody fragments comprise a FR4 region selected from the group consisting of: JH4, Jκ1, and Jλ2/3. 6. The collection according to claim 1 , wherein said synthetic antibody fragments further comprise a diversified HCDR3 region. 7. The collection according to claim 1 , wherein said synthetic antibody fragments further comprise a diversified LCDR3 region. 8. The collection according to claim 1 , wherein the collection comprises 1×10 4 synthetic antibody fragments.

Assignees

Inventors

Classifications

  • Complementarity determining region [CDR] · CPC title

  • C07K16/005Primary

    constructed by phage libraries · CPC title

  • Biochemical methods, e.g. using enzymes or whole viable microorganisms · CPC title

  • from primates, e.g. man · CPC title

  • General methods of preparing gene libraries, not provided for in other subgroups · CPC title

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What does patent US10647757B2 cover?
The present disclosure enables methods of identifying the VH and VL class pairs in the human immune repertoire, determining the VH and VL class pairs that are most prevalent and those having favorable biophysical properties. More specifically, the collections of the present disclosure comprise the most prevalent and/or preferred VH and VL class pairings with highly diversified CDRs.
Who is the assignee on this patent?
Morphosys Ag
What technology area does this patent fall under?
Primary CPC classification C07K16/005. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 12 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).