PXD056009 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Development of mirror-image monobodies targeting the oncogenic BCR::ABL1 kinase |
Description | Mirror-image proteins, composed of D-amino acids, are an attractive therapeutic modality, as they exhibit high metabolic stability and lack immunogenicity. Development of mirror-image binding proteins is achieved through chemical synthesis of D-target proteins, phage display library selection of L-binders and chemical synthesis of (mirror-image) D binders that consequently bind the physiological L-targets. Monobodies are well-established synthetic (L )binding proteins and their small size (~90 residues) and lack of endogenous cysteine residues make them particularly accessible to chemical synthesis. Here, we developed monobodies with nanomolar binding affinities against the D-SH2 domain of the leukemic tyrosine kinase BCR::ABL1. Two crystal structures of heterochiral monobody-SH2 complexes revealed targeting of the pY binding pocket by an unconventional binding mode. We then prepared potent D-monobodies by either ligating two chemically synthesized D-peptides or by self-assembly without ligation. Their proper folding and stability were determined and high affinity binding to the L-target was shown. D-monobodies were protease-resistant, showed long-term plasma stability, inhibited BCR::ABL1 kinase activity and bound BCR::ABL1 in cells and (to some extent in) cell lysates with high selectivity. Hence, we demonstrate that functional D monobodies can be developed readily. Our work represents an important step towards the possible future therapeutic use of D-monobodies when combined with emerging methods to enable cytoplasmic delivery of monobodies. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-28 |
AnnouncementXML | Submission_2024-10-28_07:54:30.009.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Uwe Linne |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | No PTMs are included in the dataset |
Instrument | timsTOF Pro |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-09-19 03:38:25 | ID requested | |
⏵ 1 | 2024-10-28 07:54:30 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: monobodies, oncogenic BCR::ABL1 kinase,Mirror-image-monobodies |
Contact List
Dr. Uwe Linne |
contact affiliation | Philipps-University Marburg Faculty of Chemistry Core Facility for Mass Spectrometry Hans-Meerwein-Str. 4 35032 Marburg |
contact email | linneu@staff.uni-marburg.de |
lab head | |
Uwe Linne |
contact affiliation | Head of Core Facility Mass Spectrometry, Faculty of Chemistry, Philipps-University Marburg |
contact email | linneu@staff.uni-marburg.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD056009
- Label: PRIDE project
- Name: Development of mirror-image monobodies targeting the oncogenic BCR::ABL1 kinase