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yuehe ding

yuehe ding

CRISPR, Aging, RNAi, LC-MS/MS, Proteomics, NGS
Worcester, City of Worcester, Worcester

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About yuehe ding:

Biological researcher with 15 years of research experiences including four years in Aging, five years in Protein Mass spectrometry and seven years in Small RNA biology and RNAi. In total, I have 8 publications in Nature Cell Biology, Elife, Cell reports, JBC, Analytical Chemistry etc. as first or co-first author and 25 additional publications as co-authors. Experienced in project management, experiment design, data analysis, data presentation and publication. 

Skilled in Biochemistry, Molecular biology, Genetics and computer science as below. 
Biochemistry – HPLC ,UPLC,Proteomics, LC-MS/MS, Protein Mass spec, Protein Posttranslational Modifications (PTM) analysis, Protein Expression and Purification, Kinase Assay, Western Blot, Silver Staining, SDS-PAGE, etc. 
Molecular biology – DNA/RNA Next Generation Sequencing, Genome Sequencing, Small RNA Cloning and Sequencing, NGS, RNA/DNA FISH, Confocal Microscopy, CHIP, RT-qPCR, Northern Blot, Molecular Cloning, etc.
Genetics – CRISPR Genome Editing, C. elegans, Transgenic worms, MosSCI, RNAi, Genetic Screening, Genotyping, etc.
Computer science – Data analysis, R, Perl, Image J, Microsoft office, Adobe illustrator, etc.

Experience

Instructor                                                        02/2023-now                | UMass Chan Medical School, Worcester, US

Post-doctoral Associate                       02/2016-01/2023           | UMass Chan Medical School, Worcester, US

Advisor: Craig C. Mello, Laureate of Nobel Prize in 2006 for Discovering RNAi

  • Developed C-BERST to define subnuclear proteomic landscapes at specific genomic loci using dCas9-APEX2. 
  • Identified HDA-1 and SUMO as novel regulators of the piRNA pathway through genetic screening. 
  • Identified HDA-1 SUMOylation sites and demonstrated that this modification is critical for its complex assembly and recruitment by the piRNA pathway. 
  • Demonstrated the SUMO E3 ligase-like activity of PIE-1, through quantitative SUMO proteomics. 
  • Developed a protein-RNA tethering system, which led to the discovery of a self-enforcing mechanism of the piRNA pathway. 
  • Applied next-generation sequencing strategies, including mRNA seq, genome seq, and small RNA seq, to study the silencing mechanism of the piRNA pathway. 
  • Mentored PhD students to achieve their academic goals.

Post-doctoral Researcher        07/2012-02/2016           | National Institute of Biological Sciences, Beijing, China

Advisor: Meng-Qiu Dong, Postdoc of John Yates III, Pioneer of Protein Mass Spec and Proteomics

  • Introduced amine-sulfhydryl and amine-carboxyl cross-linkers to increase the depth of cross-linking mass spectrometry and applied that information for modeling protein-protein interaction. 
  • Developed arginine-selective chemical cross-linkers to improve mass spec analysis of protein structures. 
  • Modeled protein excited-state structures from "over-length" chemical cross-links. 
  • Developed DynaXL to visualize the ensemble structures of protein complexes using spatial information obtained from cross-linking mass spectrometry. 
  • Developed open-pFind, an open search engine for comprehensive identification of peptides from ms2 spectra. 
  • Identified STIMATE as a regulator of Ca2+ influx by proteomics mapping of ER-PM junctions using proximal labeling (APEX). 
  • Applied cross-linking mass spectrometry to study complex assembly, including exocyst complex, ATG2B-WDR45 complex, PI3KC3 complex, etc. 
  • Identified phosphorylation sites of LSD1 by PLK1 and MYPT1 by Chk1 with HRAM MS and HCD fragmentation. 
  • Identified O-GlcNAcylation sites of Polη during translesion DNA synthesis with HRAM MS and HCD fragmentation. 

Education

 

Advisor: Meng-Qiu Dong, Postdoc of John Yates III, Pioneer of Protein Mass Spec and Proteomics

  • Studied the functions of a gene family that were highly increased in the long-lived daf-2 mutant. 
  • Discovered the crosstalk between CAMKII/Calcineurin and the insulin pathway in lifespan regulation. 
  • Identified the Actin K84me by ALKBH4 using Mass spectrometry. 
  • Conducted quantitative proteomics, PTM identification and developed CXMS methods to elucidate protein structures. 
  • Developed cross-linking mass spectrometry methods to study protein folding and protein-protein interactions. 
  • Developed search engine pLink to identify cross-linked peptides from complex samples after cross-linking. 
  • Developed high-speed cross-linking search engine pLink2 which is 40 times faster than pLink1. 

B.S. |Biotechnology | University of Science and Technology of China (USTC), China 09/2003– 07/2007

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