T
Tina Wang
Researcher at Broad Institute
Publications - 19
Citations - 1049
Tina Wang is an academic researcher from Broad Institute. The author has contributed to research in topics: Methylglyoxal & Directed evolution. The author has an hindex of 10, co-authored 18 publications receiving 598 citations. Previous affiliations of Tina Wang include Howard Hughes Medical Institute & Harvard University.
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Journal ArticleDOI
Continuous evolution of SpCas9 variants compatible with non-G PAMs.
Shannon M. Miller,Tina Wang,Tina Wang,Tina Wang,Peyton B. Randolph,Peyton B. Randolph,Peyton B. Randolph,Mandana Arbab,Mandana Arbab,Mandana Arbab,Max W. Shen,Tony P. Huang,Tony P. Huang,Tony P. Huang,Zaneta Matuszek,Gregory A. Newby,Gregory A. Newby,Gregory A. Newby,Holly A. Rees,Holly A. Rees,Holly A. Rees,David R. Liu,David R. Liu,David R. Liu +23 more
TL;DR: Three new SpCas9 variants that collectively recognize NRNH PAMs are reported that enable targeting of most NR PAM sequences and substantially reduce the fraction of genomic sites that are inaccessible by Cas9-based methods.
Journal ArticleDOI
A “Turn-On” Fluorescent Sensor for Methylglyoxal
TL;DR: It is shown that MBo is selective for MGO over other biologically relevant dicarbonyls and is suitable for detecting MGO in complex environments, including that of living cells, and its utility in estimating plasma concentrations of MGO is demonstrated.
Journal ArticleDOI
Regulatory myeloid cells paralyze T cells through cell-cell transfer of the metabolite methylglyoxal.
Tobias Baumann,Andreas Dunkel,Christian Schmid,Sabine Schmitt,Michael Hiltensperger,Kerstin Lohr,Vibor Laketa,Sainitin Donakonda,Uwe Ahting,Bettina Lorenz-Depiereux,Jan E. Heil,Johann Schredelseker,Luca Simeoni,Caroline Fecher,Nina Körber,Tanja Bauer,Norbert Hüser,Daniel Hartmann,Melanie Laschinger,Kilian Eyerich,Stefanie Eyerich,Martina Anton,Matthew D. Streeter,Tina Wang,Burkhart Schraven,David Spiegel,Farhah Assaad,Thomas Misgeld,Hans Zischka,Peter J. Murray,Annkristin Heine,Annkristin Heine,Mathias Heikenwalder,Thomas Korn,Corinna Dawid,Thomas Hofmann,Percy A. Knolle,Bastian Höchst +37 more
TL;DR: It is reported that human MDSCs were characterized by strongly reduced metabolism and conferred this compromised metabolic state to CD8 + T cells, thereby paralyzing their effector functions and identifying the dicarbonyl methylglyoxal as a marker metabolite for MDSC that mediates T cell paralysis and can serve as a target to improve cancer immune therapy.
Journal ArticleDOI
Base editing of haematopoietic stem cells rescues sickle cell disease in mice.
Gregory A. Newby,Gregory A. Newby,Gregory A. Newby,Jonathan Yen,Kaitly J. Woodard,Thiyagaraj Mayuranathan,Cicera R. Lazzarotto,Yichao Li,Heather Sheppard-Tillman,Shaina N. Porter,Yu Yao,Kalin Mayberry,Kelcee A. Everette,Kelcee A. Everette,Kelcee A. Everette,Yoonjeong Jang,Christopher J. Podracky,Christopher J. Podracky,Christopher J. Podracky,Elizabeth Thaman,Christophe Lechauve,Akshay Sharma,Jordana M. Henderson,Michelle Richter,Michelle Richter,Michelle Richter,Kevin T. Zhao,Kevin T. Zhao,Kevin T. Zhao,Shannon M. Miller,Shannon M. Miller,Shannon M. Miller,Tina Wang,Tina Wang,Tina Wang,Luke W. Koblan,Luke W. Koblan,Luke W. Koblan,Anton P. McCaffrey,John F. Tisdale,Theodosia A. Kalfa,Theodosia A. Kalfa,Shondra M. Pruett-Miller,Shengdar Q. Tsai,Mitchell J. Weiss,David R. Liu,David R. Liu,David R. Liu +47 more
TL;DR: This article used ABE8e-NRCH to convert the β-globin allele (HBBS) into Makassar βglobin (HBBG), a non-pathogenic variant.
Journal ArticleDOI
Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks
James J. Galligan,James A. Wepy,Matthew D. Streeter,Philip J. Kingsley,Michelle M. Mitchener,Orrette R. Wauchope,William N. Beavers,Kristie L. Rose,Tina Wang,David Spiegel,Lawrence J. Marnett +10 more
TL;DR: The existence of Lys and Arg modifications on histones derived from a glycolytic by-product, methylglyoxal (MGO), demonstrate the existence of a previously undetected histone modification and provide a link between cellular metabolism and the histone code.