journal article·2021

Electric field modulated peptide based hydrogel nanocatalysts

Jahnu Saikia, K. Dharmalingam, R. Anandalakshmi, Amay Sanjay Redkar, Venugopal T. Bhat, Vibin Ramakrishnan

Soft Matter· Volume 17· Issue 42
Publisher page

Abstract

The ability to modulate self-assembly is the key to manufacture application-oriented materials. In this study, we investigated the effect of three independent variables that can modulate the catalytic activity of self-assembling peptides. The first two variables, amino acid sequence and its stereochemistry, were examined for their specific roles in the epitaxial growth and hydrogelation properties of a series of catalytic tripeptides. We observed that aromatic π-π interactions that direct the self-assembly of designed peptides, and the catalytic properties of hydrogels, are governed by the position and chirality of the proline residue. Subsequently, the influence of the third variable, an external electric field, was also tested to confirm its catalytic efficiency for the asymmetric C-C bond-forming aldol reaction. In particular, the electric field treated pff and PFF gels showed 10 and 36% higher stereoselectivity, respectively, compared with the control. Structure-property analysis using CD and FTIR spectroscopy indicates the electric field-induced beta to non-beta conformational transition in the peptide secondary structure, which corroborates with its reduced cross-link density and fibril width, respectively. Amplitude sweep rheology of the gels suggests a decrease in the storage modulus, with increased field strength. The results showed that an electric field of optimal strength can modulate the physical characteristics of the hydrogel, which in turn is manifested in the observed difference in enantioselectivity.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Lipid Membrane Structure and Behavior · Photoreceptor and optogenetics research

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

Affiliations

Molecular Informatics and Design Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Assam 781039, India

Advanced Energy & Materials Systems Laboratory, Department of Chemical Engineering, Indian Institute of Technology Guwahati, Assam 781039, India

Organic Synthesis and Catalysis Laboratory SRM Research Institute and Department of Chemistry SRM Institute of Science and Technology, Tamil Nadu 603203, India

Funding

Department of Biotechnology, Ministry of Science and Technology, India · University Grants Commission

References (88)

Show source-provided references
1. Hawkins · J. Am. Chem. Soc. · 2020 · 142 · 437910.1021/jacs.9b13156 ↗
2. Orbach · Langmuir · 2012 · 28 · 201510.1021/la204426q ↗
3. Guler · J. Am. Chem. Soc. · 2007 · 129 · 1208210.1021/ja075044n ↗
4. Singh · Chem. – Eur. J. · 2017 · 23 · 98110.1002/chem.201602624 ↗
5. Zhang · ACS Nano · 2014 · 8 · 1171510.1021/nn5051344 ↗
6. Wang · Chem. Soc. Rev. · 2016 · 45 · 558910.1039/C6CS00176A ↗
7. Kang · Macromolecules · 2016 · 49 · 99410.1021/acs.macromol.5b02148 ↗
8. Tao · Chem. Soc. Rev. · 2016 · 45 · 393510.1039/C5CS00889A ↗
9. Chen · Cryst. Growth Des. · 2018 · 18 · 276510.1021/acs.cgd.7b01503 ↗
10. Dadhwal · RSC Adv. · 2020 · 10 · 923410.1039/D0RA01013H ↗
11. Smith · Adv. Mater. · 2008 · 20 · 3710.1002/adma.200701221 ↗
12. Orbach · Biomacromolecules · 2009 · 10 · 264610.1021/bm900584m ↗
13. Du · Chem. Rev. · 2015 · 115 · 1316510.1021/acs.chemrev.5b00299 ↗
14. Dasgupta · RSC Adv. · 2013 · 3 · 911710.1039/c3ra40234g ↗
15. Tang · Langmuir · 2009 · 25 · 944710.1021/la900653q ↗
16. Löwik · Chem. Soc. Rev. · 2010 · 39 · 339410.1039/b914342b ↗
17. Haines · J. Am. Chem. Soc. · 2005 · 127 · 1702510.1021/ja054719o ↗
18. Lawrence · Catal. Sci. Technol. · 2021 · 11 · 238610.1039/D1CY00189B ↗
19. Dreher · J. Am. Chem. Soc. · 2008 · 130 · 68710.1021/ja0764862 ↗
20. Ni · RSC Adv. · 2018 · 8 · 2948210.1039/C8RA04391D ↗
21. Martin · Nat. Commun. · 2018 · 9 · 110.1038/s41467-017-02088-w ↗
22. Pandey · Sci. Rep. · 2017 · 7 · 110.1038/s41598-016-0028-x ↗
23. Gazit · Chem. Soc. Rev. · 2007 · 36 · 126310.1039/b605536m ↗
24. Ye · Colloids Surf., A · 2014 · 452 · 16510.1016/j.colsurfa.2014.03.084 ↗
25. Hirst · J. Am. Chem. Soc. · 2003 · 125 · 901010.1021/ja036111q ↗
26. Wang · J. Am. Chem. Soc. · 2005 · 127 · 1637210.1021/ja055800u ↗
27. Son · Acta Biomater. · 2018 · 67 · 14710.1016/j.actbio.2017.11.048 ↗
28. Roth-Konforti · Macromol. Rapid Commun. · 2018 · 39 · 180058810.1002/marc.201800588 ↗
29. Ma · Small · 2015 · 11 · 178710.1002/smll.201402140 ↗
30. Nguyen · Nat. Commun. · 2016 · 7 · 1
31. Youn · J. Comput. Chem. · 2016 · 37 · 97110.1002/jcc.24284 ↗
32. Jenkins · Nano Energy · 2018 · 51 · 31710.1016/j.nanoen.2018.06.061 ↗
33. Saikia · ACS Chem. Neurosci. · 2019 · 10 · 225010.1021/acschemneuro.8b00490 ↗
34. Kwon · ACS Appl. Mater. Interfaces · 2020 · 12 · 5559610.1021/acsami.0c16000 ↗
35. Pandey · RSC Adv. · 2019 · 9 · 474410.1039/C8RA09993F ↗
36. Song · Chem. Commun. · 2020 · 56 · 1149710.1039/D0CC04466K ↗
37. Velichko · Adv. Funct. Mater. · 2012 · 22 · 36910.1002/adfm.201101538 ↗
38. Rodríguez-Llansola · Chem. Commun. · 2009 · 730310.1039/b916250j ↗
39. Rodríguez-Llansola · Chem. – Eur. J. · 2010 · 16 · 848010.1002/chem.201000654 ↗
40. Berdugo · Chem. Commun. · 2013 · 49 · 1060810.1039/c3cc45623d ↗
41. Machajewski · Angew. Chem., Int. Ed. · 2000 · 39 · 135210.1002/(SICI)1521-3773(20000417)39:8<1352::AID-ANIE1352>3.0.CO;2-J ↗
42. Mukaiyama · Angew. Chem., Int. Ed. · 2004 · 43 · 559010.1002/anie.200300641 ↗
43. Lindström · Chem. Rev. · 2002 · 102 · 275110.1021/cr010122p ↗
44. List · J. Am. Chem. Soc. · 2000 · 122 · 239510.1021/ja994280y ↗
45. Panday · Tetrahedron: Asymmetry · 2011 · 22 · 181710.1016/j.tetasy.2011.09.013 ↗
46. Notz · J. Am. Chem. Soc. · 2000 · 122 · 738610.1021/ja001460v ↗
47. Mlynarski · Chem. Soc. Rev. · 2008 · 37 · 150210.1039/b710577k ↗
48. Huang · Nanoscale Res. Lett. · 2014 · 9 · 110.1186/1556-276X-9-1 ↗
49. Fuentes-Caparrós · Biomacromolecules · 2021 · 22 · 162510.1021/acs.biomac.1c00078 ↗
50. Datta · Soft Matter · 2019 · 15 · 482710.1039/C9SM00343F ↗
51. Tian · J. Controlled Release · 2007 · 121 · 13710.1016/j.jconrel.2007.05.010 ↗
52. Mase · Org. Biomol. Chem. · 2010 · 8 · 404310.1039/c004970k ↗
53. Lu · Chem. Sci. · 2013 · 4 · 96510.1039/C2SC21300A ↗
54. Kleinschmidt · J. Colloid Interface Sci. · 2020 · 559 · 7610.1016/j.jcis.2019.10.005 ↗
55. Zhao · J. Org. Chem. · 2012 · 77 · 478410.1021/jo300569c ↗
56. Rodriguez-Llansola · J. Am. Chem. Soc. · 2009 · 131 · 1147810.1021/ja902589f ↗
57. Rodríguez-Llansola · Org. Biomol. Chem. · 2009 · 7 · 309110.1039/b904523f ↗
58. Bellotto · Soft Matter · 2020 · 16 · 1015110.1039/D0SM01191F ↗
59. Tena-Solsona · Chem. – Eur. J. · 2016 · 22 · 668710.1002/chem.201600344 ↗
60. Copeland · J. Org. Chem. · 1998 · 63 · 678410.1021/jo981642w ↗
61. Fichman · Acta Biomater. · 2014 · 10 · 167110.1016/j.actbio.2013.08.013 ↗
62. Lozano · J. Mater. Chem. · 2011 · 21 · 886210.1039/c1jm10505a ↗
63. J. L.Tymoczko , J. M.Berg and L.Stryer , Biochemistry: a short course , Macmillan , 2011
64. Sakthivel · J. Am. Chem. Soc. · 2001 · 123 · 526010.1021/ja010037z ↗
65. Kofoed · Bioorg. Med. Chem. Lett. · 2003 · 13 · 244510.1016/S0960-894X(03)00498-0 ↗
66. Xie · Small · 2017 · 13 · 170099910.1002/smll.201700999 ↗
67. Tao · Langmuir · 2011 · 27 · 272310.1021/la1034273 ↗
68. Tokuyama · J. Membr. Sci. · 2020 · 595 · 11753310.1016/j.memsci.2019.117533 ↗
69. Mouarrawis · Front. Chem. · 2018 · 6 · 62310.3389/fchem.2018.00623 ↗
70. Bandak · Pharm. Res. · 1999 · 16 · 84110.1023/A:1018869818282 ↗
71. Wood · J. Clin. Pharm. Ther. · 1990 · 15 · 29110.1111/j.1365-2710.1990.tb00387.x ↗
72. Claessens · J. Phys. Org. Chem. · 1997 · 10 · 25410.1002/(SICI)1099-1395(199705)10:5<254::AID-POC875>3.0.CO;2-3 ↗
73. Gazit · FASEB J. · 2002 · 16 · 7710.1096/fj.01-0442hyp ↗
74. Reches · Science · 2003 · 300 · 62510.1126/science.1082387 ↗
75. Reches · Nano Lett. · 2004 · 4 · 58110.1021/nl035159z ↗
76. Sasidharan · J. Phys. Chem. B · 2017 · 121 · 40410.1021/acs.jpcb.6b09474 ↗
77. Melchionna · Curr. Top. Med. Chem. · 2016 · 16 · 200910.2174/1568026616999160212120302 ↗
78. Garcia · ACS Nano · 2021 · 15 · 301510.1021/acsnano.0c09386 ↗
79. Frederix · Nat. Chem. · 2015 · 7 · 3010.1038/nchem.2122 ↗
80. Li · Appl. Environ. Microbiol. · 2014 · 80 · 342610.1128/AEM.00016-14 ↗
81. Castillo · Electrophoresis · 2008 · 29 · 502610.1002/elps.200800260 ↗
82. Arslan · Adv. Healthcare Mater. · 2014 · 3 · 135710.1002/adhm.201300491 ↗
83. Zotova · J. Am. Chem. Soc. · 2007 · 129 · 1510010.1021/ja0738881 ↗
84. Pelin · Catal. Sci. Technol. · 2019 · 9 · 430410.1039/C9CY00790C ↗
85. List · Synlett · 2001 · 167510.1055/s-2001-18074 ↗
86. Notz · Acc. Chem. Res. · 2004 · 37 · 58010.1021/ar0300468 ↗
87. Mandalapu · Synlett · 2015 · 707
88. Conde · Chem. Sci. · 2012 · 3 · 148610.1039/c2sc20199b ↗