Author

M. A. Carpenter

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Cancer Biology· 1 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:human· 4 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:protein structure prediction· 1 Assay:structural biology· 1

Frequent Co-Authors

R. S. Harris· 3 shared A. Z. Cheng· 1 shared D. A. Harki· 1 shared D. Sauter· 1 shared D. Yee· 1 shared H. Aihara· 1 shared H. Nasser· 1 shared K. Shi· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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3 shared papersMicrobiology

R. S. Harris

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

APOBEC3 degradation is the primary function of HIV-1 Vif for virus replication in the myeloid cell line THP-1

T. Ikeda, R. Shimizu, H. Nasser, M. A. Carpenter, A. Z. Cheng, W. L. Brown, D. Sauter, R. S. Harris

This study shows that HIV-1 Vif primarily degrades A3 enzymes to enable viral replication in THP-1 cells, as disrupting A3 proteins restores infectivity of Vif-deficient viruses.

bioRxiv · Mar 28, 2023 · PreprintMicrobiology

Rad51 inhibition sensitizes non-replicating quiescent cells to UVB radiation and transcription stress

S. Khan, M. A. Carpenter, M. G. Kemp

The paper shows Rad51 promotes survival of quiescent cells under UVB and transcription stress, independent of NER.

bioRxiv · Sep 20, 2022 · PreprintCell Biology

Mutational impact of APOBEC3A and APOBEC3B in a human cell line and comparisons to breast cancer

M. A. Carpenter, N. A. Temiz, M. Ibrahim, M. Jarvis, M. Brown, P. Argyris, W. Brown, D. Yee, R. S. Harris

This study quantifies the mutagenic activities of APOBEC3A and APOBEC3B in a human cell line and compares their mutation signatures to breast cancer genomes, showing both enzymes contribute to the mutation landscape.

bioRxiv · Apr 26, 2022Cancer Biology

Active site plasticity and possible modes of chemical inhibition of the human DNA deaminase APOBEC3B

K. Shi, O. Demir, M. A. Carpenter, S. Banerjee, D. A. Harki, R. E. Amaro, R. S. Harris, H. Aihara

This study reports structures of APOBEC3B with loop 7 from APOBEC3G, revealing inactive conformations stabilized by small molecules, providing insights for inhibitor design.

bioRxiv · Jan 7, 2019Biochemistry