Colorimetric protein sensing using catalytically amplified sensor arrays

Small

Volumn 8, Issue 23, 2012, Pages 3589-3592

  Li, Xiaoning ^a   Wen, Fang ^b   Creran, Brian ^a   Jeong, Youngdo ^a   Zhang, Xinrong ^b   Rotello, Vincent M ^a  

^a UNIVERSITY OF MASSACHUSETTS   (United States)

^b TSINGHUA UNIVERSITY   (China)

Author keywords

colorimetry; iron oxide nanoparticles; protein sensing; sensor arrays

Indexed keywords

ANALYTES; CATIONIC MONOLAYERS; COLORIMETRIC SENSING; IDENTIFICATION OF PROTEINS; IRON OXIDE NANOPARTICLE; PROTEIN SENSING; RECOGNITION ELEMENT; SIGNAL AMPLIFIERS; SIGNAL PATTERNS;

COLOR; COLORIMETRY; METAL NANOPARTICLES; MONOLAYERS; SENSOR ARRAYS; SENSORS;

PROTEINS;

FERRIC ION; FERRIC OXIDE; NANOPARTICLE; PEROXIDASE; PROTEIN;

CATALYSIS; CHEMISTRY; COLORIMETRY; GENETIC PROCEDURES; METABOLISM; PROCEDURES;

BIOSENSING TECHNIQUES; CATALYSIS; COLORIMETRY; FERRIC COMPOUNDS; NANOPARTICLES; PEROXIDASE; PROTEINS;

EID: 84870601948     PISSN: 16136810     EISSN: 16136829     Source Type: Journal    
DOI: 10.1002/smll.201201549     Document Type: Article

References (42)

1. M. C. Mullenix, S. Wiltshire, W. P. Shao, G. Kitos, B. Schweitzer, Clin. Chem. 2001, 47, 1926-1929.
2. S. F. Kingsmore, D. D. Patel, Curr. Opin. Biotechnol. 2003, 14, 74-81.
3. J. Okuno, K. Maehashi, K. Kerman, Y. Takamura, K. Matsumoto, E. Tamiya, Biosens. Bioelectron. 2007, 22, 2377-2381.
4. N. L. Anderson, N. G. Anderson, Mol. Cell. Proteomics 2002, 1, 845-867.
5. L. Hartwell, D. Mankoff, A. Paulovich, S. Ramsey, E. Swisher, Nat. Biotechnol. 2006, 24, 905-908.
6. A. Larsson, M. E. Johansson, S. Wangefjord, A. Gaber, B. Nodin, P. Kucharzewska, C. Welinder, M. Belting, J. Eberhard, A. Johnsson, M. Uhlen, K. Jirstrom, Br. J. Cancer 2011, 105, 666-672.
7. a) D. H. Charych, J. O. Nagy, W. Spevak, M. D. Bednarski, Science 1993, 261, 585-588
8. b) N. T. K. Thanh, Z. Rosenzweig, Anal. Chem. 2002, 74, 1624-1628
9. c) M. Sastry, N. Lala, V. Patil, S. P. Chavan, A. G. Chittiboyina, Langmuir 1998, 14, 4138-4142
10. d) H. A. Ho, A. Najari, M. Leclerc, Acc. Chem. Res. 2008, 41, 168-178.
11. a) R. Elghanian, J. J. Storhoff, R. C. Mucic, R. L. Letsinger, C. A. Mirkin, Science 1997, 277, 1078-1081
12. b) J. J. Storhoff, R. Elghanian, R. C. Mucic, C. A. Mirkin, R. L. Letsinger, J. Am. Chem. Soc. 1998, 120, 1959-1964
13. c) D. Aili, R. Selegard, L. Baltzer, K. Enander, B. Liedberg, Small 2009, 5, 2445-2452
14. d) C. C. Huang, Y. F. Huang, Z. H. Cao, W. H. Tan, H. T. Chang, Anal. Chem. 2005, 77, 5735-5741.
15. a) N. A. Rakow, K. S. Suslick, Nature 2000, 406, 710-713
16. b) J. J. Lavigne, S. M. Savoy, M. B. Clevenger, J. E. Ritchie, B. McDoniel, S. J. Yoo, E. V. Anslyn, J. T. McDevitt, J. B. Shear, D. P. Neikirk, J. Am. Chem. Soc. 1998, 120, 6429-6430.
17. a) C. C. You, O. R. Miranda, B. Gider, P. S. Ghosh, I. B. Kim, B. Erdogan, S. A. Krovi, U. H. F. Bunz, V. M. Rotello, Nat. Nanotechnol. 2007, 2, 318-323
18. b) M. De, S. Rana, H. Akpinar, O. R. Miranda, R. R. Arvizo, U. H. F. Bunz, V. M. Rotello, Nat. Chem. 2009, 1, 461-465
19. c) K. J. Albert, N. S. Lewis, C. L. Schauer, G. A. Sotzing, S. E. Stitzel, T. P. Vaid, D. R. Walt, Chem. Rev. 2000, 100, 2595-2626.
20. a) J. F. Folmer-Andersen, M. Kitamura, E. V. Anslyn, J. Am. Chem. Soc. 2006, 128, 5652-5653
21. b) N. T. Greene, K. D. Shimizu, J. Am. Chem. Soc. 2005, 15, 5695-5700
22. c) C. Zhang, K. S. Suslick, J. Am. Chem. Soc. 2005, 127, 11548-11549
23. d) O. R. Miranda, H. T. Chen, C. C. You, D. E. Mortenson, X. C. Yang, U. H. F. Bunz, V. M. Rotello, J. Am. Chem. Soc. 2010, 132, 5285-5289.
24. O. R. Miranda, X. Li, L. Garcia-Gonzalez, Z.-J. Zhu, B. Yan, U. H. F. Bunz, V. M. Rotello, J. Am. Chem. Soc. 2011, 133, 9650-9653.
25. a) E. Shoji, M. S. Freund, J. Am. Chem. Soc. 2001, 123, 3383-3384
26. b) H. Wei, E. Wang, Anal. Chem. 2008, 80, 2250-2254.
27. a) Y. Jv, B. X. Li, R. Cao, Chem. Commun. 2010, 46, 8017-8019
28. b) Y. J. Song, K. G. Qu, C. Zhao, J. S. Ren, X. G. Qu, Adv. Mater. 2010, 22, 2206-2210
29. c) Y. J. Guo, L. Deng, J. Li, S. J. Guo, E. K. Wang, S. J. Dong, ACS Nano 2011, 5, 1282-1290
30. d) G. Pelossof, R. Tel-Vered, J. Elbaz, I. Willner, Anal. Chem. 2010, 82, 4396-4402.
31. M. J. Wiester, P. A. Ulmann, C. A. Mirkin, Angew. Chem. Int. Ed. 2011, 50, 114-137.
32. L. Z. Gao, J. Zhuang, L. Nie, J. B. Zhang, Y. Zhang, N. Gu, T. H. Wang, J. Feng, D. L. Yang, S. Perrett, X. Yan, Nat. Nanotechnol. 2007, 2, 577-583.
33. A. Asati, S. Santra, C. Kaittanis, S. Nath, J. M. Perez, Angew. Chem. Int. Ed. 2009, 48, 2308-2312.
34. M. Ornatska, E. Sharpe, D. Andreescu, S. Andreescu, Anal. Chem. 2011, 83, 4273-4280.
35. L. Z. Gao, J. M. Wu, S. Lyle, K. Zehr, L. L. Cao, D. Gao, J. Phys. Chem. C 2008, 112, 17357-17361.
36. K. S. Park, M. I. Kim, D. Y. Cho, H. G. Park, Small 2011, 7, 1521-1525.
37. In our study, we found that hemoglobin had an enhancement in OD response instead of inhibition (see Supporting Information, Figure S1 and Figure S2). We believe this is due to the peroxidatic activity of the heme group in hemoglobin. Reference: a), H. F. Bunn, J. H. Jandl, J. Biol. Chem. 1968, 243, 465-475
38. b) M. J. Karnovsky, J. Cell. Biol. 1967, 35, 213-236.
39. The data from five replicates of ten proteins with two NPs were used to generate the training matrix. The training matrix was emplyed for the classic LDA in SYSTAT (version 11.0, Systat Software, Richmond, CA 94804, USA, 2004).
40. a) C. Hou, J. Dong, G. Zhang, Y. Lei, M. Yang, Y. Zhang, Z. Liu, S. Zhang, D. Huo, Biosens. Bioelectron. 2011, 26, 3981-3986
41. b) Z. S. Wu, H. X. Lu, X. P. Liu, R. Hu, H. Zhou, G. L. Shen, R. Q. Yu, Anal. Chem. 2010, 82, 3890-3898
42. c) A. T. Wright, M. J. Griffin, Z. L. Zhong, S. C. McCleskey, E. V. Anslyn, J. T. McDevitt, Angew. Chem., Int. Ed. 2005, 44, 6375-6378.