RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000083.xml
PDF herunterladen
Synlett 2017; 28(09): 1005-1010
DOI: 10.1055/s-0036-1588721
DOI: 10.1055/s-0036-1588721
synpacts
Pattern-Generating Unimolecular Sensors: For Future Differential Sensing and Molecular Computing
Authors
Weitere Informationen
Publikationsverlauf
Received: 26. November 2016
Accepted after revision: 24. Januar 2017
Publikationsdatum:
16. Februar 2017 (online)
Abstract
Pattern-generating unimolecular sensors are an innovative class of analytical and computing systems that utilize inherent molecular mechanisms to create multiple optical responses in a manner similar to that in which arrays of small reporter molecules can be engineered to function as cross-reactive sensors. Pattern-generating unimolecular sensors can detect and discriminate between a wide range of chemical and biochemical analytes, and they can also be used in computation, where they function as molecular logic devices utilizing chemometric analysis. This feature article summarizes the various pattern-generating approaches and their miniaturization to a unimolecular level in the fields of differential sensing and molecular computing.
-
References
- 1a Persaud K, Dodd G. Nature 1982; 299: 352-352
- 1b Dentoni L, Capelli L, Sironi S, Del Rosso R, Zanetti S, Della Torre M. Sensors 2012; 12: 14363-14363
- 2a Capelli L, Sironi S, Del Rosso R. Sensors 2014; 14: 19979-19979
- 2b Rock F, Barsan N, Weimar U. Chem. Rev. 2008; 108: 705-705
- 2c Turner AP. F, Magan N. Nat. Rev. Microbiol. 2004; 2: 161-161
- 2d Wilson AD, Baietto M. Sensors 2009; 9: 5099-5099
- 2e Tisch U, Haick H. Rev. Chem. Eng. 2010; 26: 171-171
- 3a de Silva AP, Gunaratne HQ. N, Gunnlaugsson T, Huxley AJ. M, McCoy CP, Rademacher JT, Rice TE. Chem. Rev. 1997; 97: 1515-1515
- 3b Callan JF, de Silva AP, Magri DC. Tetrahedron 2005; 61: 8551-8551
- 3c Sinkeldam RW, Greco NJ, Tor Y. Chem. Rev. 2010; 110: 2579-2579
- 3d Domaille DW, Que EL, Chang CJ. Nat. Chem. Biol. 2008; 4: 168-168
- 4a Griffin AB, Adams SR, Tsien RY. Science 1998; 281: 269-269
- 4b Giepmans BN. G, Adams SR, Ellisman MH, Tsien RY. Science 2006; 312: 217-217
- 5a Tomat E, Lippard SJ. Curr. Opin. Chem. Biol. 2010; 14: 225-225
- 5b James TD, Phillips MD, Shinkai S. Boronic Acids in Saccharide Recognition . RSC; Cambridge: 2006
- 5c Bull SD, Davidson MG, van den Elsen JM. H, Fossey JS, Jenkins AT. A, Jiang Y.-B, Kubo Y, Marken F, Sakurai K, Zhao J, James TD. Acc. Chem. Res. 2013; 46: 312-312
- 5d Sakamoto T, Ojida A, Hamachi I. Chem. Commun. 2009; 141-141
- 5e Sessler JL, Gale PA, Cho W.-S. In Anion Receptor Chemistry . Stoddart JF. Royal Society of Chemistry; Cambridge: 2006: 320
- 6a Tian H. Angew. Chem. Int. Ed. 2010; 49: 4710-4710
- 6b de Silva AP, Gunaratne HQ. N, McCoy CP. A. Nature 1993; 364: 42-42
- 6c de Silva AP, Uchiyama S. Nat. Nanotechnol. 2007; 2: 399-399
- 6d Pischel U, Andréasson J, Gust D, Pais VF. ChemPhysChem 2013; 14: 28-28
- 6e de Ruiter G, van den Boom ME. Acc. Chem. Res. 2011; 44: 563-563
- 6f Amelia M, Zou L, Credi A. Coord. Chem. Rev. 2010; 254: 2267-2267
- 6g Andréasson J, Pischel U. Chem. Soc. Rev. 2015; 44: 1053-1053
- 7 Magri DC, Brown GJ, McClean GD, de Silva AP. J. Am. Chem. Soc. 2006; 128: 4950-4950
- 8a de Silva AP. Beilstein J. Org. Chem. 2015; 11: 2774-2774
- 8b Uchiyama S, Fukatsu E, McClean GD, de Silva AP. Angew. Chem. Int. Ed. 2016; 55: 768-768
- 8c de Silva AP, Uchiyama S. Top. Curr. Chem. 2011; 300: 1-1
- 9a de Silva AP, James MR, McKinney BO. F, Pears DA, Weir SM. Nat. Mater. 2006; 5: 787-787
- 9b Uchiyama S, Iwai K, de Silva A. Angew. Chem. Int. Ed. 2008; 47: 4609-4609
- 9c Yuan L, Lin W, Xie Y, Chen B, Zhu S. J. Am. Chem. Soc. 2012; 134: 1305-1305
- 9d Ling J, Naren G, Kelly J, Moody TS, de Silva AP. J. Am. Chem. Soc. 2015; 137: 3763-3763
- 10 Gardner JW, Bartlett PN. Electronic Noses: Principles and Applications . Oxford University Press; Oxford: 1999
- 11a Miranda OR, Creran B, Rotello VM. Curr. Opin. Chem. Biol. 2010; 14: 728-728
- 11b Umali AP, Anslyn EV. Curr. Opin. Chem. Biol. 2010; 14: 685-685
- 11c Severin K. Curr. Opin. Chem. Biol. 2010; 14: 737-737
- 11d Anzenbacher PJr, Liu Y.-l, Kozelkova ME. Curr. Opin. Chem. Biol. 2010; 14: 693-693
- 11e Shimizu KD, Stephenson CJ. Curr. Opin. Chem. Biol. 2010; 14: 743-743
- 11f Musto CJ, Suslick KS. Curr. Opin. Chem. Biol. 2010; 14: 758-758
- 11g Walt DR. Curr. Opin. Chem. Biol. 2010; 14: 767-767
- 11h Stojanovic MN, Worgall TS. Curr. Opin. Chem. Biol. 2010; 14: 751-751
- 12a Askima JR, Mahmoudiab M, Suslick KS. Chem. Soc. Rev. 2013; 42: 8649-8649
- 12b Anzenbacher PJr, Lubal P, Buček P, Palacios MA, Kozelkova ME. Chem. Soc. Rev. 2010; 39: 3954-3954
- 12c Lavigne JJ, Anslyn EV. Angew. Chem. Int. Ed. 2001; 40: 3118-3118
- 13 Lozano J, de la Vega PM, Martinez E, Alvarez F, Morera J, Aguilera T. Chem. Eng. Trans. 2010; 23: 165-165 ; DOI: 10.3303/CET1023028
- 14a Margulies D, Hamilton AD. J. Am. Chem. Soc. 2009; 131: 9142-9142
- 14b Margulies D, Hamilton AD. Curr. Opin. Chem. Biol. 2010; 14: 705-705
- 15a Rout B, Unger L, Armony G, Iron MA, Margulies D. Angew. Chem. Int. Ed. 2012; 51: 12477-12477
- 15b Rout B, Milko P, Iron MA, Motiei L, Margulies D. J. Am. Chem. Soc. 2013; 135: 15330-15330
- 15c Sarkar T, Selvakumar K, Motiei L, Margulies D. Nat. Commun. 2016; 7: 11374-11374
- 15d Rout B, Motiei L, Margulies D. Synlett 2014; 25: 1050-1050
- 16 Rout B. Sci. Rep. 2016; 6: 27115-27115
- 17a Dolmans DE, Fukumura D, Jain RK. Nat. Rev. Cancer 2003; 3: 380-380
- 17b O’Conner A, Gallagher WA, Byrne AT. Photochem. Photobiol. 2009; 85: 1053-1053
- 18a Wilson BC, Patterson MS, Lilge L. Laser Med. Sci. 1997; 12: 182-182
- 18b Mustafa FH, Jaafer MS. Indian J. Phys. 2013; 87: 203-203
- 19 Slastnikova TA, Rosenkranz AA, Lupanova TN, Gulak PV, Gnuchev NV, Sobolev AS. Dokl. Biochem. Biophys. 2012; 446: 235-235
- 20 Anslyn EV. J. Org. Chem. 2007; 72: 687-687
- 21a Teichert JF, Mazunin D, Bode JW. J. Am. Chem. Soc. 2013; 135: 11314-11314
- 21b Larson KK, He M, Teichert JF, Naganawa A, Bode JW. Chem. Sci. 2012; 3: 1825-1825
- 22a Komatsu H, Citterio D, Fujiwara Y, Minamihashi K, Araki Y, Hagiwara M, Suzuki K. Org. Lett. 2005; 7: 2857-2857
- 22b Nelson TL, O’Sullivan C, Greene NT, Maynor MS, Lavigne JJ. J. Am. Chem. Soc. 2006; 128; 5640-128; 5640
- 22c Lee B, Chen S, Heinis C, Scopelliti R, Severin K. Org. Lett. 2013; 15; 3456-15; 3456
- 23a Peri-Naor R, Ilani T, Motiei L, Margulies D. J. Am. Chem. Soc. 2015; 137: 9507-9507
- 23b Erbas-Cakmak S, Bozdemir OA, Cakmak Y, Akkaya EU. Chem. Sci. 2013; 4: 858-858
- 23c Amir RJ, Popkov M, Lerner RA, Barbas CF, Shabat D. Angew. Chem. Int. Ed. 2005; 44: 4378-4378
- 23d Kolpashchikov DM, Stojanovic MN. J. Am. Chem. Soc. 2005; 127: 11348-11348
- 23e Douglas SM, Bachelet I, Church GM. Science 2012; 335: 831-831
- 23f Xie Z, Wroblewska L, Prochazka L, Weiss R, Benenson Y. Science 2011; 333: 1307-1307
For selected reviews, see:
For metals, see:
For saccharides, see:
For phosphates, see:
For anions, see:
For small-molecule-based logic-gate therapy, see:
For DNA computing-based therapy see: