Engineering Two‐Helix Motifs through NDI Linker: A Modular Approach for Charge Transferable Conductive Foldamers Design
Source abstract
Abstract
Abstract A new approach for the construction of two‐helix motifs from helix modules and planar 1,4,5,8‐naphthalenetetracarboxylic diimide (NDI) is described. The single crystal conformations of two different types of two‐helix motifs consisting of achiral α‐peptide C10‐helix (310) and chiral α,γ‐hybrid peptide C12‐helix revealed that the helices adopted antiparallel orientations across the planar NDI with 2‐fold symmetry. The crystal conformations of two‐helix motifs were further explored to design electrical conducting peptide foldamer by introducing electron rich pyrene (p‐type) as a side‐chain in the α,γ‐hybrid helix. The two‐helix motif with charge transferable pyrene (p‐type)‐NDI (n‐type) combination showed better electrical conductivity compared to the two‐helix motif without pyrene side‐chain. Moreover, the crystal conformations also provided molecular insight into the peptide orientation of NDI‐peptide conjugates. The two‐helix motifs described here may serve as potential molecular scaffolds to design novel conductive peptide foldamers and self‐assembling biomaterials.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Chemical Synthesis and Analysis · Supramolecular Self-Assembly in Materials · Photochromic and Fluorescence Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry Indian Institute of Science Education and Research-Pune (IISER−P) Dr. Homi Bhabha Road Pune- 411 008 India
Funding
Science and Engineering Research Board
References (100+)
Show source-provided references
1.
2. 10.1038/nchembio87610.1038/nchembio876 ↗
3. 10.1021/cr000045i10.1021/cr000045i ↗
4. 10.1021/cr000053z10.1021/cr000053z ↗
5. 10.1021/ar960298r10.1021/ar960298r ↗
6.
7. 10.1016/S1359-0278(97)00029-110.1016/S1359-0278(97)00029-1 ↗
8. 10.1039/a700624a10.1039/a700624a ↗
9. 10.1073/pnas.98.3.87010.1073/pnas.98.3.870 ↗
10.
11. 10.1002/chem.20120432710.1002/chem.201204327 ↗
12. 10.1039/C6CC00127K10.1039/C6CC00127K ↗
13.
14. 10.1039/c1cc11137j10.1039/c1cc11137j ↗
15. 2007
16. 10.1038/375303a010.1038/375303a0 ↗
17. 10.1021/ja00047a06810.1021/ja00047a068 ↗
18. 10.1021/ja982452610.1021/ja9824526 ↗
19. 10.1021/ja00116a03610.1021/ja00116a036 ↗
20. 10.1021/jacs.7b0796110.1021/jacs.7b07961 ↗
21.
22. 10.1002/adma.20090362810.1002/adma.200903628 ↗
23. 10.1002/adma.20120154410.1002/adma.201201544 ↗
24. 10.1021/acs.accounts.7b0043410.1021/acs.accounts.7b00434 ↗
25. 10.1002/anie.20160483310.1002/anie.201604833 ↗
26. 10.1002/ange.20160483310.1002/ange.201604833 ↗
27. 10.1039/C6CC01983H10.1039/C6CC01983H ↗
28. 10.1021/acs.chemrev.6b0016010.1021/acs.chemrev.6b00160 ↗
29.
30. 10.1016/j.chempr.2016.06.01310.1016/j.chempr.2016.06.013 ↗
31. 10.1021/acs.inorgchem.5b0248010.1021/acs.inorgchem.5b02480 ↗
32. 10.1021/cm802071w10.1021/cm802071w ↗
33. 10.1039/C5SC04450B10.1039/C5SC04450B ↗
34. 10.1016/j.ccr.2011.03.01310.1016/j.ccr.2011.03.013 ↗
35.
36. 10.1021/acs.jpcc.5b0339810.1021/acs.jpcc.5b03398 ↗
37. 10.1021/ja509480u10.1021/ja509480u ↗
38.
39. 10.1039/C5SC04906G10.1039/C5SC04906G ↗
40. 10.1002/anie.20120970810.1002/anie.201209708 ↗
41. 10.1002/ange.20120970810.1002/ange.201209708 ↗
42.
43. 10.1002/anie.20130968010.1002/anie.201309680 ↗
44. 10.1002/ange.20130968010.1002/ange.201309680 ↗
45. 10.1002/chem.20120401610.1002/chem.201204016 ↗
46. 10.1021/ja048080k10.1021/ja048080k ↗
47.
48. 10.1039/B809359H10.1039/B809359H ↗
49. 10.1021/ol300607m10.1021/ol300607m ↗
50. 10.1016/j.biomaterials.2013.09.04410.1016/j.biomaterials.2013.09.044 ↗
51.
52. 10.1021/jacs.8b0080910.1021/jacs.8b00809 ↗
53. 10.1002/anie.20170773010.1002/anie.201707730 ↗
54. 10.1002/ange.20170773010.1002/ange.201707730 ↗
55.
56. 10.1002/anie.20140381610.1002/anie.201403816 ↗
57. 10.1002/ange.20140381610.1002/ange.201403816 ↗
58. 10.1002/anie.20150457610.1002/anie.201504576 ↗
59. 10.1002/ange.20150457610.1002/ange.201504576 ↗
60. 10.1021/jacs.6b0208610.1021/jacs.6b02086 ↗
61. 10.1021/cm070457910.1021/cm0704579 ↗
62.
63. 10.1002/anie.20060334810.1002/anie.200603348 ↗
64. 10.1002/ange.20060334810.1002/ange.200603348 ↗
65. 10.1039/c0ob00027b10.1039/c0ob00027b ↗
66. 10.1039/c1ob06147j10.1039/c1ob06147j ↗
67. 10.1002/anie.20060489110.1002/anie.200604891 ↗
68. 10.1002/ange.20060489110.1002/ange.200604891 ↗
69. 10.1002/anie.20070498310.1002/anie.200704983 ↗
70. 10.1002/ange.20070498310.1002/ange.200704983 ↗
71. 10.1021/ja208864710.1021/ja2088647 ↗
72.
73. 10.1039/c0cc00078g10.1039/c0cc00078g ↗
74. 10.1021/ja404753r10.1021/ja404753r ↗
75. 10.1002/anie.20120951310.1002/anie.201209513 ↗
76. 10.1002/ange.20120951310.1002/ange.201209513 ↗
77. 10.1039/C3TC32377C10.1039/C3TC32377C ↗
78. 10.1021/ja906377q10.1021/ja906377q ↗
79. 10.1002/chem.20130485710.1002/chem.201304857 ↗
80.
81. 10.1021/ar300296910.1021/ar3002969 ↗
82. 10.1021/acs.bioconjchem.5b0049710.1021/acs.bioconjchem.5b00497 ↗
83. 10.1002/adfm.20110100110.1002/adfm.201101001 ↗
84. 10.1021/acs.langmuir.6b0272710.1021/acs.langmuir.6b02727 ↗
85. 10.1039/C4NR04340E10.1039/C4NR04340E ↗
86. 10.1021/jacs.7b0400610.1021/jacs.7b04006 ↗
87. 10.1039/C7CS00817A10.1039/C7CS00817A ↗
88. 10.1039/C5CC01996F10.1039/C5CC01996F ↗
89. 10.1039/C6OB02786E10.1039/C6OB02786E ↗
90.
91. 10.1021/ol500307p10.1021/ol500307p ↗
92. 10.1021/ol300987d10.1021/ol300987d ↗
93. 10.1021/ja00373a01810.1021/ja00373a018 ↗
94.
95. 10.1002/anie.20130839610.1002/anie.201308396 ↗
96. 10.1002/ange.20130839610.1002/ange.201308396 ↗
97. 10.1002/chem.20130337910.1002/chem.201303379 ↗
98. 10.1039/C6NR01128D10.1039/C6NR01128D ↗
99. 10.1039/c0cc00249f10.1039/c0cc00249f ↗
100.