Vivian T. Dien

ORCID: 0000-0003-3237-4325
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About
Contact & Profiles
Research Areas
  • RNA and protein synthesis mechanisms
  • Genomics and Phylogenetic Studies
  • Advanced biosensing and bioanalysis techniques
  • DNA and Nucleic Acid Chemistry
  • Cancer Genomics and Diagnostics
  • Molecular Biology Techniques and Applications
  • Chemical Synthesis and Analysis
  • Microbial Metabolic Engineering and Bioproduction
  • Antimicrobial Peptides and Activities
  • Adsorption and biosorption for pollutant removal
  • Bacterial Genetics and Biotechnology
  • RNA modifications and cancer
  • Advanced Biosensing Techniques and Applications
  • Geochemistry and Elemental Analysis
  • Single-cell and spatial transcriptomics
  • Heavy metals in environment
  • Click Chemistry and Applications

Elements Biosciences (United States)
2023-2024

Scripps Research Institute
2017-2020

Massachusetts Institute of Technology
2013

Fluorescent bioorthogonal smart probes across the visible spectrum will enable sensitive visualization of metabolically labeled molecules in biological systems. Here we present a unified design, based on principle photoinduced electron transfer, to access panel highly fluorogenic azide that are activated by conversion corresponding triazoles via click chemistry. Termed CalFluors, these possess emission maxima range from green far red wavelengths, and biomolecule detection under no-wash...

10.1021/jacs.5b02383 article EN Journal of the American Chemical Society 2015-04-22

Abstract We present avidity sequencing, a sequencing chemistry that separately optimizes the processes of stepping along DNA template and identifying each nucleotide within template. Nucleotide identification uses multivalent ligands on dye-labeled cores to form polymerase–polymer–nucleotide complexes bound clonal copies targets. These polymer–nucleotide substrates, termed avidites, decrease required concentration reporting nucleotides from micromolar nanomolar yield negligible dissociation...

10.1038/s41587-023-01750-7 article EN cc-by Nature Biotechnology 2023-05-25

Previously, we reported the creation of a semi-synthetic organism (SSO) that stores and retrieves increased information by virtue stably maintaining an unnatural base pair (UBP) in its DNA, transcribing corresponding nucleotides into codons anticodons mRNAs tRNAs, then using them to produce proteins containing noncanonical amino acids (ncAAs). Here report systematic extension effort optimize SSO exploring variety deoxy- ribonucleotide analogues. Importantly, this includes first vivo...

10.1021/jacs.9b02075 article EN Journal of the American Chemical Society 2019-06-26

We have developed a family of unnatural base pairs (UBPs), exemplified by the pair formed between dNaM and dTPT3, for which pairing is mediated not complementary hydrogen bonding but hydrophobic packing forces. These UBPs enabled creation first semisynthetic organisms (SSOs) that store increased genetic information use it to produce proteins containing noncanonical amino acids. However, retention was poor in some sequence contexts. Here, optimize SSO, we synthesize two novel...

10.1021/jacs.8b08416 article EN Journal of the American Chemical Society 2018-11-12

We have developed an unnatural base pair (UBP) and a semisynthetic organism (SSO) that imports the constituent nucleoside triphosphates uses them to replicate DNA containing UBP. However, propagation of UBP is at least in part limited by stability triphosphates, which are degraded cellular secreted phosphatases. To circumvent this problem, we now report synthesis evaluation with their β,γ-bridging oxygen replaced difluoromethylene moiety, yielding dNaMTPCF2 dTPT3TPCF2. find although cannot...

10.1021/jacs.6b12731 article EN Journal of the American Chemical Society 2017-02-07

We report the use of a simple yet highly effective magnetite-waste tea composite to remove lead(II) (Pb2+) ions from water. Magnetite-waste composites were dispersed in four different types water–deionized (DI), artificial rainwater, groundwater and freshwater–that mimic actual environmental conditions. The water samples had varying initial concentrations (0.16–5.55 ppm) Pb2+ mixed with for at least 24 hours allow adsorption reach equilibrium. stable all 3 months could be easily removed...

10.1371/journal.pone.0066648 article EN cc-by PLoS ONE 2013-06-20
Sinan Arslan Francisco J. Blanco García Minghao Guo Matthew W. Kellinger Semyon Kruglyak and 95 more Jake A. LeVieux Adeline H. Mah Haosen Wang Junhua Zhao Chunhong Zhou Andrew Altomare J. Kevin Bailey Matthew B. Byrne Chiting Chang Steve X. Chen Claudia N. Dennler Vivian T. Dien Derek Fuller Ryan Kelley Omid Khandan Michael Klein Michael Kim Bryan R. Lajoie Bill Lin Yu Liu Tyler Lopez Peter T. Mains Andrew Price Samantha R. Robertson Hermes Taylor‐Weiner Ramreddy Tippana Austin B. Tomaney Su Zhang Mark R. Ambroso Rosita Bajari Ava M. Bellizzi Chris B. Benitez D. R. Bérard Lorenzo Berti Kelly Blease Angela P. Blum Andrew M. Boddicker Leo Bondar Chris Brown Chris A. Bui Juan Calleja-Aguirre Kevin Cappa Joshua Chan Victor W.-C. Chang Katherine Charov Xiyi Chen Rodger M. Constandse Ryan C. Costello Weston Damron Mariam Dawood Nicole DeBuono John D. Dimalanta Laure Edoli Keerthana Elango Nikka Faustino Chao Feng Mathhew Ferrari Keith Frankie Adam Fries Anne Galloway Vlad Gavrila Gregory J. Gemmen James Ghadiali Arash Ghorbani Logan A. Goddard Adriana R. Guetter Garren L. Hendricks Jendrik Hentschel Daniel J. Honigfort Yun-Ting Hsieh Yu-Hsien Hwang Fu Scott Im Chaoyi Jin Shradha Kabu Daniel E. Kincade Shawn Levy Yu Li Vincent Liang William H. Light Jonathan B. Lipsher Tsung-li Liu Grace Long Rui Ma John M. Mailloux Kyle A. Mandla Anyssa R. Martinez Max Mass Daniel T. McKean Michael Meron Celyne S. Moh Rachel Moore Juan Moreno Jordan M. Neysmith Cassandra S. Niman Jesus M. Nunez

Abstract We present avidity sequencing - a novel chemistry that separately optimizes the process of stepping along DNA template and identifying each nucleotide within template. Nucleotide identification uses multivalent ligands on dye-labeled cores to form polymerase-polymer complexes bound clonal copies targets. These polymer-nucleotide substrates, termed avidites, decrease required concentration reporting nucleotides from micromolar nanomolar, yield negligible dissociation rates....

10.1101/2022.11.03.514117 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-11-04

Abstract We present a novel sequencing chemistry implemented as part of the AVITI system. Relying on proximal DNA binding sites created through amplification solid support, avidity uses multivalent nucleotide ligands dye-labeled cores to simultaneously form polymerase-polymer complexes bound clonal copies targets. These polymer-nucleotide substrates, termed avidites, decrease required concentration reporting nucleotides by 100x and yield negligible dissociation rate. demonstrate use avidites...

10.21203/rs.3.rs-1965701/v1 preprint EN cc-by Research Square (Research Square) 2022-11-10

Abstract The accuracy of a sequencing platform has traditionally been measured by the %Q30, or percentage data exceeding basecall 99.9%. Improvements to beyond Q30 may be beneficial for certain applications such as identification low frequency alleles improvement reference genomes. Here we demonstrate how achieved over 70% Q50 (99.999% accuracy) on AVITI™ sequencer. This level required us not only improve quality but also mitigate library preparation errors and analysis artifacts.

10.1101/2024.02.01.578321 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-02-05
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