journal article·2021-09-29Open access

Modulation of Gold Nanorod Growth via the Proteolysis of Dithiol Peptides for Enzymatic Biomarker Detection

Matthew N. Creyer, Zhicheng Jin, Colman Moore, Wonjun Yim, Jiajing Zhou, Jesse V. Jokerst

ACS Applied Materials & Interfaces· Volume 13· Issue 38

Abstract

Gold nanorods possess optical properties that are tunable and highly sensitive to variations in their aspect ratio (length/width). Therefore, the development of a sensing platform where the gold nanorod morphology (i.e., aspect ratio) is modulated in response to an analyte holds promise in achieving ultralow detection limits. Here, we use a dithiol peptide as an enzyme substrate during nanorod growth. The sensing mechanism is enabled by the substrate design, where the dithiol peptide contains an enzyme cleavage site in-between cysteine amino acids. When cleaved, the peptide dramatically impacts gold nanorod growth and the resulting optical properties. We demonstrate that the optical response can be correlated with enzyme concentration and achieve a 45 pM limit of detection. Furthermore, we extend this sensing platform to colorimetrically detect tumor-associated inhibitors in a biologically relevant medium. Overall, these results present a subnanomolar method to detect proteases that are critical biomarkers found in cancers, infectious diseases, and inflammatory disorders.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Advanced biosensing and bioanalysis techniques · Advanced Nanomaterials in Catalysis

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

Affiliations

Department of Nanoengineering, University of California, La Jolla, San Diego, California 92093, United States

Materials Science and Engineering Program, University of California, La Jolla, San Diego, California 92093, United States

Department of Radiology, University of California, La Jolla, San Diego, California 92093, United States

Funding

National Cancer Institute · National Institute of Dental and Craniofacial Research · Achievement Rewards for College Scientists Foundation · National Science Foundation

References (62)

Show source-provided references
1. 10.1021/acsnano.0c0521510.1021/acsnano.0c05215 ↗
2. 10.1021/acsami.1c0099310.1021/acsami.1c00993 ↗
3. 10.1021/nn304347g10.1021/nn304347g ↗
4. 10.1039/d0bm01063d10.1039/d0bm01063d ↗
5. 10.1021/ja801631c10.1021/ja801631c ↗
6. 10.1016/j.jcis.2018.02.05310.1016/j.jcis.2018.02.053 ↗
7. 10.1039/c8tb00368h10.1039/c8tb00368h ↗
8. 10.3390/nano1011223910.3390/nano10112239 ↗
9. 10.1007/s11468-011-9228-110.1007/s11468-011-9228-1 ↗
10. 10.1021/acsnano.0c0279710.1021/acsnano.0c02797 ↗
11. 10.1021/cr400062310.1021/cr4000623 ↗
12. 10.1039/c7nr06367a10.1039/c7nr06367a ↗
13. 10.1021/acssensors.6b0022910.1021/acssensors.6b00229 ↗
14. 10.1021/acs.nanolett.8b0297310.1021/acs.nanolett.8b02973 ↗
15. 10.1021/la102559e10.1021/la102559e ↗
16. 10.1039/c1cs15237h10.1039/c1cs15237h ↗
17. 10.1021/cm303708p10.1021/cm303708p ↗
18. 10.1021/jp990183f10.1021/jp990183f ↗
19. 10.1021/nl202559p10.1021/nl202559p ↗
20. 10.1021/acs.chemmater.0c0248210.1021/acs.chemmater.0c02482 ↗
21. 10.1002/adma.20120169010.1002/adma.201201690 ↗
22. 10.1201/9780429295188-210.1201/9780429295188-2 ↗
23. 10.1021/acs.accounts.9b0028810.1021/acs.accounts.9b00288 ↗
24. 10.1021/cm303661d10.1021/cm303661d ↗
25. 10.1021/nn300315j10.1021/nn300315j ↗
26. 10.1002/adfm.20170052310.1002/adfm.201700523 ↗
27. 10.1021/acs.langmuir.0c0030210.1021/acs.langmuir.0c00302 ↗
28. 10.1021/acs.analchem.0c0032110.1021/acs.analchem.0c00321 ↗
29. 10.1016/j.nantod.2013.08.00810.1016/j.nantod.2013.08.008 ↗
30. 10.1021/acs.analchem.9b0457310.1021/acs.analchem.9b04573 ↗
31. 10.1039/c4nr01323a10.1039/c4nr01323a ↗
32. 10.1039/c9tc00757a10.1039/c9tc00757a ↗
33. 10.1016/j.snb.2018.03.02310.1016/j.snb.2018.03.023 ↗
34. 10.1016/j.snb.2020.12880610.1016/j.snb.2020.128806 ↗
35. 10.1021/acs.analchem.7b0260810.1021/acs.analchem.7b02608 ↗
36. 10.1021/acsami.0c0343310.1021/acsami.0c03433 ↗
37. 10.1021/acs.analchem.0c0470410.1021/acs.analchem.0c04704 ↗
38. 10.1021/acs.jpclett.5b0212310.1021/acs.jpclett.5b02123 ↗
39. 10.1021/acsnano.8b0965810.1021/acsnano.8b09658 ↗
40. 10.1021/jp408259610.1021/jp4082596 ↗
41. 10.1021/jp057170o10.1021/jp057170o ↗
42. 10.1021/cm303659q10.1021/cm303659q ↗
43. 10.1021/acs.nanolett.9b0243410.1021/acs.nanolett.9b02434 ↗
44. 10.1002/ange.20110730410.1002/ange.201107304 ↗
45. 10.1021/acs.nanolett.5b0308810.1021/acs.nanolett.5b03088 ↗
46. Armbruster D. A. · Clin. Biochem. Rev. · 2008 · 29 · S49
47. 10.1016/j.micron.2010.09.00810.1016/j.micron.2010.09.008 ↗
48. 10.1021/acs.jpcc.6b0850910.1021/acs.jpcc.6b08509 ↗
49. 10.1021/nn506155r10.1021/nn506155r ↗
50. 10.1021/la035570210.1021/la0355702 ↗
51. 10.1021/la047735s10.1021/la047735s ↗
52. 10.1021/jp050797m10.1021/jp050797m ↗
53. 10.1021/jp502401w10.1021/jp502401w ↗
54. 10.1021/cm050685810.1021/cm0506858 ↗
55. 10.1021/ja071050810.1021/ja0710508 ↗
56. 10.1073/pnas.96.3.89310.1073/pnas.96.3.893 ↗
57. 10.1073/pnas.060782610410.1073/pnas.0607826104 ↗
58. 10.1038/s41565-019-0365-610.1038/s41565-019-0365-6 ↗
59. 10.1002/ijc.291030011010.1002/ijc.2910300110 ↗
60. 10.3109/0036551910910462210.3109/00365519109104622 ↗
61. 10.1038/bjc.1986.17610.1038/bjc.1986.176 ↗
62. 10.1002/ijc.291031060610.1002/ijc.2910310606 ↗