Zobrazeno 1 - 10
of 23
pro vyhledávání: '"David Nedrud"'
Autor:
Christian B. Macdonald, David Nedrud, Patrick Rockefeller Grimes, Donovan Trinidad, James S. Fraser, Willow Coyote-Maestas
Publikováno v:
Genome Biology, Vol 24, Iss 1, Pp 1-19 (2023)
Abstract Insertions and deletions (indels) enable evolution and cause disease. Due to technical challenges, indels are left out of most mutational scans, limiting our understanding of them in disease, biology, and evolution. We develop a low cost and
Externí odkaz:
https://doaj.org/article/11399c52db2f4426b21268f10cf7d139
Autor:
Willow Coyote-Maestas, David Nedrud, Antonio Suma, Yungui He, Kenneth A. Matreyek, Douglas M. Fowler, Vincenzo Carnevale, Chad L. Myers, Daniel Schmidt
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Here, the authors perform a large-scale, high-throughput biochemical assay to determine the compatibility of over 300,000 domain recombination variants of the inward rectifier K+ channel Kir2.1. They derive rules for designing domain insertion varian
Externí odkaz:
https://doaj.org/article/446c0c0118e64afe931272b243499af9
Publikováno v:
eLife, Vol 11 (2022)
A long-standing goal in protein science and clinical genetics is to develop quantitative models of sequence, structure, and function relationships to understand how mutations cause disease. Deep mutational scanning (DMS) is a promising strategy to ma
Externí odkaz:
https://doaj.org/article/15c4d948595e4756b6a890ffb7da5841
Autor:
Mareike D. Hoffmann, Alina C. Zdechlik, Yungui He, David Nedrud, George Aslanidi, Wendy Gordon, Daniel Schmidt
Publikováno v:
bioRxiv
Evolved properties of Adeno-Associated Virus (AAV), such as broad tropism and immunogenicity in humans, are barriers to AAV-based gene therapy. Previous efforts to re-engineer these properties have focused on variable regions near AAV’s 3-fold prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3848cbbbb957670507da90c702717afa
https://europepmc.org/articles/PMC10153220/
https://europepmc.org/articles/PMC10153220/
Autor:
Christian B. Macdonald, David Nedrud, Patrick Rockefeller Grimes, Donovan Trinidad, James S. Fraser, Willow Coyote-Maestas
Insertions and deletions (indels) are a major source of genetic variation in evolution and the cause of nearly 30% of Mendelian disease. Despite their importance, indels are left out of nearly every systematic mutational scan to date due to technical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d3c1051ed8660ce8b15749b799d8a4
https://doi.org/10.1101/2022.07.26.501589
https://doi.org/10.1101/2022.07.26.501589
Publikováno v:
Proteins: Structure, Function, and Bioinformatics. 89:899-914
Deep mutational scanning (DMS) facilitates data-driven models of protein structure and function. Here, we adapted Saturated Programmable Insertion Engineering (SPINE) as a programmable DMS technique. We validate SPINE with a reference single mutant d
Autor:
Kenneth A. Matreyek, Antonio Suma, David Nedrud, Yungui He, Douglas M. Fowler, Willow Coyote-Maestas, Vincenzo Carnevale, Daniel F. Schmidt, Chad L. Myers
Understanding the biophysical mechanisms that govern the combination of protein domains into viable proteins is essential for advancing synthetic biology and biomedical engineering. Here, we use massively parallel genotype/phenotype assays to determi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fc661cc9702987c58e58b08331e5aa2
https://doi.org/10.1101/2020.12.09.418442
https://doi.org/10.1101/2020.12.09.418442
Deep mutational scanning enables data-driven models of protein structure and function. Here, we adapted Saturated Programmable Insertion Engineering as an economical and programmable deep mutational scanning technique. We validate this approach with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1776917cf66261bee11aedc3bc3033
https://doi.org/10.1101/2020.06.26.174375
https://doi.org/10.1101/2020.06.26.174375