journal article·2022-06-22

Hydrogel Stamping for Rapid, Multiplexed, Point-of-Care Immunostaining of Cells and Tissues

Lip Ket Chin, Huiyan Li, Jae-Hyeok Choi, Yoshiko Iwamoto, Juhyun Oh, Jouha Min, Suk Kyung Beak, Dahyeon Yoo, Cesar M. Castro, Dongyoung Lee, Hyungsoon Im

ACS Applied Materials & Interfaces· Volume 14· Issue 24
Publisher page

Abstract

In the era of precision oncology, multicolor fluorescence imaging has become a core technology for multiplexed molecular analysis of cellular and tissue specimens. However, conventional solution-based staining is labor-intensive and time-consuming and requires considerable expertise to yield optimal results, which creates difficulties for employing this technology in resource-limited settings. Here, we report a new immunostaining method based on hydrogel stamping, which is simple, fast, easy to use, and reproducible. We showed that a hydrophilic hydrogel stamp could effectively transfer fluorescent antibodies to targets and withdraw an excess solution when the reaction is completed, obviating the need for extra washing. This unique property allows for quality immunostaining in 5 min for cells using one-eighth of antibody consumption compared to the conventional solution-based method. Furthermore, we implemented fluorescence quenching and immunocycling with hydrogel staining for multiplexed analysis of 9 protein markers at a single cell level. Finally, we applied the immunocycling method to human breast cancer tissue samples and showed quality immunostaining over a large area (∼2 cm2) in 30 min for molecular subtyping of breast cancer. The hydrogel immunostaining could open new opportunities for rapid, automated, and multiplexed profiling in compact point-of-care systems for molecular cancer diagnosis.
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Research context

OpenAlex topics: Advanced Biosensing Techniques and Applications · Single-cell and spatial transcriptomics · Molecular Biology Techniques and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge Street, CPZN 5206, Boston, Massachusetts 02114, United States

Department of Electrical Engineering, City University of Hong Kong, Kowloon 999077, Hong Kong SAR

School of Engineering, University of Guelph, 50 Stone Road East, Guelph N1G2W1, Canada

Noul Co. Limited, Gyeonggi-do, Yongin 16942, Republic of Korea

Cancer Center, Massachusetts General Hospital, Boston, Massachusetts 02114, United States

Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts 02114, United States

Funding

Ministry of Science and ICT, South Korea · Massachusetts General Hospital · Noul, Co Ltd

References (47)

Show source-provided references
1. 10.1038/d41586-020-02676-910.1038/d41586-020-02676-9 ↗
2. 10.1038/s41467-020-14381-210.1038/s41467-020-14381-2 ↗
3. 10.1016/S0140-6736(11)60993-810.1016/S0140-6736(11)60993-8 ↗
4. 10.5306/wjco.v5.i3.41210.5306/wjco.v5.i3.412 ↗
5. 10.1016/j.soc.2017.08.00510.1016/j.soc.2017.08.005 ↗
6. 10.1002/cac2.1202310.1002/cac2.12023 ↗
7. 10.1073/pnas.130013611010.1073/pnas.1300136110 ↗
8. 10.7554/eLife.3165710.7554/eLife.31657 ↗
9. 10.1016/j.ymeth.2014.08.01610.1016/j.ymeth.2014.08.016 ↗
10. 10.1038/ncomms939010.1038/ncomms9390 ↗
11. 10.1126/scitranslmed.300736110.1126/scitranslmed.3007361 ↗
12. 10.1038/s41467-018-07002-610.1038/s41467-018-07002-6 ↗
13. 10.1016/j.cell.2018.07.01010.1016/j.cell.2018.07.010 ↗
14. 10.1126/sciadv.aax585110.1126/sciadv.aax5851 ↗
15. 10.1038/nm.348810.1038/nm.3488 ↗
16. 10.1038/s41587-020-0472-910.1038/s41587-020-0472-9 ↗
17. 10.1016/j.jim.2008.02.00510.1016/j.jim.2008.02.005 ↗
18. 10.1111/his.1244610.1111/his.12446 ↗
19. 10.1038/modpathol.2016.11210.1038/modpathol.2016.112 ↗
20. 10.1016/j.acthis.2007.11.00910.1016/j.acthis.2007.11.009 ↗
21. 10.1002/cti2.118310.1002/cti2.1183 ↗
22. 10.1016/j.cels.2016.03.00810.1016/j.cels.2016.03.008 ↗
23. 10.1371/journal.pone.001044110.1371/journal.pone.0010441 ↗
24. 10.1039/d1lc00375e10.1039/d1lc00375e ↗
25. 10.1021/acsami.0c2252110.1021/acsami.0c22521 ↗
26. 10.1038/nmeth.383910.1038/nmeth.3839 ↗
27. 10.1038/s41467-021-24775-510.1038/s41467-021-24775-5 ↗
28. 10.1021/acsami.1c0254210.1021/acsami.1c02542 ↗
29. 10.1146/annurev-biophys-070317-03290510.1146/annurev-biophys-070317-032905 ↗
30. 10.1016/j.carbpol.2013.05.07610.1016/j.carbpol.2013.05.076 ↗
31. 10.3390/nano1103070310.3390/nano11030703 ↗
32. 10.1021/acsnano.8b0302910.1021/acsnano.8b03029 ↗
33. 10.1002/0471142735.im2104s10310.1002/0471142735.im2104s103 ↗
34. 10.1073/pnas.151013311210.1073/pnas.1510133112 ↗
35. Fiorelli, R.; Sidhu, G. S.; Cebrián-Silla, A.; Melendez, E. L.; Mehta, S.; Garcia-Verdugo, J. M.; Sanai, N. Enhanced Tissue Penetration of Antibodies through Pressurized Immunohistochemistry, 2020. bioRxiv:2020.09.25.311936.10.1101/2020.09.25.311936 ↗
36. 10.1038/s41598-019-41119-y10.1038/s41598-019-41119-y ↗
37. 10.1038/s41378-020-00205-210.1038/s41378-020-00205-2 ↗
38. 10.1063/1.513047810.1063/1.5130478 ↗
39. 10.1021/ac010468010.1021/ac0104680 ↗
40. 10.1038/s41378-021-00329-z10.1038/s41378-021-00329-z ↗
41. 10.1016/j.trac.2018.09.00110.1016/j.trac.2018.09.001 ↗
42. 10.1126/scitranslmed.aaz974610.1126/scitranslmed.aaz9746 ↗
43. 10.1126/scitranslmed.300204810.1126/scitranslmed.3002048 ↗
44. 10.1038/s41551-018-0265-310.1038/s41551-018-0265-3 ↗
45. 10.4049/jimmunol.170126210.4049/jimmunol.1701262 ↗
46. 10.1172/jci.insight.12296110.1172/jci.insight.122961 ↗
47. 10.1126/scitranslmed.aaf393610.1126/scitranslmed.aaf3936 ↗