I am a PhD graduate student and a Stanford ChEM-H Chemistry/Biology Interface Predoctoral Trainee at Stanford University, Department of Chemistry under the supervision of D.H. Chen Professor of Bioengineering Karl Deisseroth. I am interested in developing new chemical/protein tools to study neuroscience.
I was previously a research assistant at the Institute of Materials Research and Engineering and the Department of Chemistry at the National University of Singapore under the supervision of Provost's Chair Professor of Chemistry Xiaogang Liu. I was an Arnold and Mabel Beckman Fellow at the Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign under the supervison of Jay and Ann Schenck Professor of Chemistry Yi Lu on bio-inspired nanomaterials, metalloDNAzymes and sensors. Prior to this, in 2010, I joined the Institute of Bioengineering and Nanotechnology in the laboratories of Professor Ying Jackie Yi-Ru, Professor Zhiqiang Gao and Principal Research Scientist Yanbing Zu to work on ultrasensitive DNA nanoparticle based biosensors. Subsequently in 2014, I worked on upconversion nanomaterials for biological applications under the supervision of Professor Xiaogang Liu at the National University of Singapore and the Institute of Materials Research and Engineering. In Summer 2015, Kang Yong returned to the National University of Singapore, the Institute of Materials Research and Engineering and the Institute of Molecular and Cell Biology under the supervision of Professor Yin Thai Chan to work on semiconductor quantum dots and microfluidics applications.
I obtained my B.S. degree in Chemistry (Highest Distinction and Edmund J. James Scholar Honors) from the University of Illinois at Urbana-Champaign in 2017.
Education & Certifications
B.S. in Chemistry, University of Illinois at Urbana-Champaign, Chemistry (2017)
Karl Deisseroth, Doctoral Dissertation Advisor (AC)
- Recent Advances in the Catalytic Synthesis of 4-Quinolones CHEM 2019; 5 (5): 1059–1107
Optical Control of Metal Ion Probes in Cells and Zebrafish Using Highly Selective DNAzymes Conjugated to Upconversion Nanoparticles
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2018; 140 (50): 17656–65
Spatial and temporal distributions of metal ions in vitro and in vivo are crucial in our understanding of the roles of metal ions in biological systems, and yet there is a very limited number of methods to probe metal ions with high space and time resolution, especially in vivo. To overcome this limitation, we report a Zn2+-specific near-infrared (NIR) DNAzyme nanoprobe for real-time metal ion tracking with spatiotemporal control in early embryos and larvae of zebrafish. By conjugating photocaged DNAzymes onto lanthanide-doped upconversion nanoparticles (UCNPs), we have achieved upconversion of a deep tissue penetrating NIR 980 nm light into 365 nm emission. The UV photon then efficiently photodecages a substrate strand containing a nitrobenzyl group at the 2'-OH of adenosine ribonucleotide, allowing enzymatic cleavage by a complementary DNA strand containing a Zn2+-selective DNAzyme. The product containing a visible FAM fluorophore that is initially quenched by BHQ1 and Dabcyl quenchers is released after cleavage, resulting in higher fluorescent signals. The DNAzyme-UCNP probe enables Zn2+ sensing by exciting in the NIR biological imaging window in both living cells and zebrafish embryos and detecting in the visible region. In this study, we introduce a platform that can be used to understand the Zn2+ distribution with spatiotemporal control, thereby giving insights into the dynamical Zn2+ ion distribution in intracellular and in vivo models.
View details for DOI 10.1021/jacs.8b09867
View details for Web of Science ID 000454383400047
View details for PubMedID 30427666
View details for PubMedCentralID PMC6473182
- Gapping into Ultrahigh Surface-Enhanced Raman Scattering Amplification ACS CENTRAL SCIENCE 2018; 4 (2): 137–39
- The improved sensitive detection of C-reactive protein based on the chemiluminescence immunoassay by employing monodispersed PAA-Au/Fe3O4 nanoparticles and zwitterionic glycerophosphoryl choline JOURNAL OF MATERIALS CHEMISTRY B 2017; 5 (21): 3919–26
DNAzyme sensors for detection of metal ions in the environment and imaging them in living cells
CURRENT OPINION IN BIOTECHNOLOGY
2017; 45: 191–201
The on-site and real-time detection of metal ions is important for environmental monitoring and for understanding the impact of metal ions on human health. However, developing sensors selective for a wide range of metal ions that can work in the complex matrices of untreated samples and cells presents significant challenges. To meet these challenges, DNAzymes, an emerging class of metal ion-dependent enzymes selective for almost any metal ion, have been functionalized with fluorophores, nanoparticles and other imaging agents and incorporated into sensors for the detection of metal ions in environmental samples and for imaging metal ions in living cells. Herein, we highlight the recent developments of DNAzyme-based fluorescent, colorimetric, SERS, electrochemical and electrochemiluminscent sensors for metal ions for these applications.
View details for DOI 10.1016/j.copbio.2017.03.002
View details for Web of Science ID 000403138500026
View details for PubMedID 28458112
View details for PubMedCentralID PMC5503749
A Broadly Applicable Assay for Rapidly and Accurately Quantifying DNA Surface Coverage on Diverse Particles
2017; 28 (4): 933–43
DNA-modified particles are used extensively for applications in sensing, material science, and molecular biology. The performance of such DNA-modified particles is greatly dependent on the degree of surface coverage, but existing methods for quantitation can only be employed for certain particle compositions and/or conjugation chemistries. We have developed a simple and broadly applicable exonuclease III (Exo III) digestion assay based on the cleavage of phosphodiester bonds-a universal feature of DNA-modified particles-to accurately quantify DNA probe surface coverage on diverse, commonly used particles of different compositions, conjugation chemistries, and sizes. Our assay utilizes particle-conjugated, fluorophore-labeled probes that incorporate two abasic sites; these probes are hybridized to a complementary DNA (cDNA) strand, and quantitation is achieved via cleavage and digestion of surface-bound probe DNA via Exo III's apurinic endonucleolytic and exonucleolytic activities. The presence of the two abasic sites in the probe greatly speeds up the enzymatic reaction without altering the packing density of the probes on the particles. Probe digestion releases a signal-generating fluorophore and liberates the intact cDNA strand to start a new cycle of hybridization and digestion, until all fluorophore tags have been released. Since the molar ratio of fluorophore to immobilized DNA is 1:1, DNA surface coverage can be determined accurately based on the complete release of fluorophores. Our method delivers accurate, rapid, and reproducible quantitation of thiolated DNA on the surface of gold nanoparticles, and also performs equally well with other conjugation chemistries, substrates, and particle sizes, and thus offers a broadly useful assay for quantitation of DNA surface coverage.
View details for DOI 10.1021/acs.bioconjchem.6b00660
View details for Web of Science ID 000399965800012
View details for PubMedID 28156100
View details for PubMedCentralID PMC5648061