Single-Cell Phenotypic Analysis and Digital Molecular Detection Linkable by a Hydrogel Bead-Based Platform
Abstract
Cell heterogeneity, such as antibiotic heteroresistance and cancer cell heterogeneity, has been increasingly observed. To probe the underlying molecular mechanisms in the dynamically changing heterogeneous cells, a high throughput platform is urgently needed to establish single cell genotype-phenotype correlations. Herein, we report a platform combining single-cell viability phenotypic analysis with digital molecular detection for bacterial cells. The platform utilizes polyethylene glycol hydrogel that cross-links through a thiol-Michael addition, which is biocompatible, fast, and spontaneous. To generate uniform nanoliter-sized hydrogel beads (Gelbeads), we developed a convenient and disposable device made of needles and microcentrifuge tubes. Gelbead-based single cell viability and molecular detection assays were established. Enhanced thermal stability and uncompromised efficiency were achieved for digital polymerase chain reaction (PCR) and digital loop-mediated isothermal amplification (LAMP) within the Gelbeads. Reagent exchange for in situ PCR following viability phenotypic analyses was demonstrated. The combined analyses may address the genotypic differences between cellular subpopulations exhibiting distinct phenotypes. The platform promises unique perspectives in mechanism elucidation of environment-evolution interaction that may be extended to other cell types for medical research.
Additional Information
© 2021 The Authors. Published by American Chemical Society. Made available through a Creative Commons CC-BY License. Received: December 15, 2020; Accepted: February 1, 2021; Published: February 12, 2021. We thank Dr. Katharina Urmann for helpful discussions. Author Contributions: The manuscript was written through contributions of all authors. M.R.H, X.H., and Y.Z. conceived the concept for this study. J.L., X.H., X.L., and Y.Z. designed the study. Y.Z. performed experiments, and J.L. and Y.Z. analyzed the data and wrote the paper. All authors approved of the manuscript. The authors acknowledge the financial support provided by the Bill and Melinda Gates Foundation (grant nos. OPP1111252 and OPP1192379). The authors declare no competing financial interest.Attached Files
Published - acsabm.0c01615.pdf
Submitted - 848168.full.pdf
Supplemental Material - mt0c01615_si_001.zip
Supplemental Material - mt0c01615_si_002.avi
Supplemental Material - mt0c01615_si_003.pdf
Files
Name | Size | Download all |
---|---|---|
md5:cc2c700824ab93f777109b39d2ee7896
|
993.8 kB | Preview Download |
md5:2f545c5971b229c6fd2a4baa9d9aa64b
|
5.6 kB | Preview Download |
md5:a1b01ea1d17021f23ad6c3040e6665e3
|
1.1 MB | Preview Download |
md5:75f28542b7214c9d5a4016cb6868b0eb
|
36.7 MB | Download |
md5:06a106bb213d421462cf00252f2b46f5
|
8.8 MB | Preview Download |
Additional details
- Alternative title
- A hydrogel beads based platform for single-cell phenotypic analysis and digital molecular detection
- PMCID
- PMC7976597
- Eprint ID
- 100040
- Resolver ID
- CaltechAUTHORS:20191125-141218051
- Bill and Melinda Gates Foundation
- OPP1111252
- Bill and Melinda Gates Foundation
- OPP1192379
- Created
-
2019-11-25Created from EPrint's datestamp field
- Updated
-
2022-02-09Created from EPrint's last_modified field