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Molecular interactions between single layered MoS2 and biological molecules

Minyu Xiao, Shuai Wei, Yaoxin Li, Joshua Jasensky, Junjie Chen, Charles L. Brooks III and Zhan Chen*
Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA. E-mail: zhanc@umich.edu

Received 13th November 2017 , Accepted 29th November 2017

First published on 30th November 2017


Two-dimensional (2D) materials such as graphene, molybdenum disulfide (MoS2), tungsten diselenide (WSe2), and black phosphorous are being developed for sensing applications with excellent selectivity and high sensitivity. In such applications, 2D materials extensively interact with various analytes including biological molecules. Understanding the interfacial molecular interactions of 2D materials with various targets becomes increasingly important for the progression of better-performing 2D-material based sensors. In this research, molecular interactions between several de novo designed alpha-helical peptides and monolayer MoS2 have been studied. Molecular dynamics simulations were used to validate experimental data. The results suggest that, in contrast to peptide–graphene interactions, peptide aromatic residues do not interact strongly with the MoS2 surface. It is also found that charged amino acids are important for ensuring a standing-up pose for peptides interacting with MoS2. By performing site-specific mutations on the peptide, we could mediate the peptide–MoS2 interactions to control the peptide orientation on MoS2.


Introduction

The unique properties of two-dimensional (2D) materials such as graphene allow ultra-sensitive electronic devices to be fabricated for gas sensing, biomolecular detection, etc.1,2 Molybdenum disulfide (MoS2), a representative 2D material, has been extensively used for sensing applications,3,4 including the construction of biosensors or for biomolecular detection.5–7 For example, previous research has reported on a MoS2-based fluorescence DNA sensor5 and the scalable production of MoS2 based biosensors with proteins.7 Biological molecules have also been reported to help facilitate the exfoliation of monolayer MoS2 flakes in the aqueous phase.8,9 We believe that it is therefore crucial to understand the interaction mechanisms between biological molecules and MoS2 surfaces in order to help the design of MoS2 based biological sensors.

Research has been performed to study molecular interactions between peptides/proteins and a MoS2 sheet using simulation methods,10–12 but experimental studies to validate such simulation results are rare. In this study, we chose an alpha-helical antimicrobial peptide, a hybrid of cecropin and melittin, as our model to investigate the molecular interactions with MoS2 using both molecular dynamics simulations and experiments.

To probe the interactions between the alpha-helical hybrid peptide and a monolayer MoS2 surface, we implemented optical microscopy with sum frequency generation (SFG) vibrational spectroscopy (Fig. 1). While optical microscopy can help us locate the positions of monolayer MoS2 flakes, SFG can enable the study of peptide/MoS2 interactions in situ with monolayer sensitivity. More details about the microscope-SFG setup can be found in the ESI.


image file: c7sc04884j-f1.tif
Fig. 1 (a) Schematic of the optical microscope-SFG setup; (b and c) AFM images of mechanically exfoliated MoS2 flakes with different magnifications. (d) Thickness measured by AFM, indicating that the MoS2 flake in (b) is a monolayer. (e) Optical image of MoS2 on a CaF2 prism surface (the circle is the focus of the visible beam for SFG data collection). According to the positions of the multilayered MoS2 flakes below the circle in both AFM (c) and optical (e) images, we can identify the monolayer MoS2 sample in the circle.

A MoS2 monolayer was not visible on a CaF2 substrate. To locate such a monolayer region, it was necessary to pre-determine a location of the monolayer MoS2 flake by AFM, using thick multilayered MoS2 regions nearby as fiducial markers (Fig. 1). Then the fiducial markers were located by SFG microscopy, and the visible and infrared beams were focused onto the nearby MoS2 monolayer region to collect the SFG spectra (Fig. 1).

SFG is a second order nonlinear optical spectroscopic technique with excellent surface selectivity; its equipment and experimental details have been published and will not be repeated here.13–21 SFG has been extensively applied to investigate molecular interactions at various interfaces, including interfaces involving polymers, water, DNA, peptides and proteins.17–19,22–28 Specifically, for alpha-helical peptides, an SFG amide I peak centered near 1650 cm−1 can be detected. The orientation of a single alpha helical peptide at an interface can be described by a tilt angle θ (the angle between the peptide main axis and the surface normal). Through analysis of the SFG amide I spectra collected using different combinations of p and s polarizations of the input/output beams, the tilt angle θ can be deduced by the measured χppp/χssp ratio.29

Materials and methods

Peptide sequence and experimental conditions

All MoS2 samples were prepared on right-angled CaF2 prisms through a mechanical exfoliation method. All peptide mutants were purchased from Peptide 2.0 and were used as received, and all peptide solutions were prepared at a concentration of 1.0 μM. Sequences of all peptides used were: wild-type hybrid peptide (KWKLFKKIGIGAVLKVLTTGLPALIS), mutant A (KAKLAKKIGIGAVLKVLTTGLPALIS), mutant B (SWSLFSSIGIGAVLKVLTTGLPALIS), and mutant C (KWKFFKKIGIGAVLKVLTTGLPALIS).

Brief description of microscope-SFG

Details about the microscope-SFG setup have been published previously.14 Briefly, to allow enough working space for an optical microscopic system, an “inverted” total internal reflection SFG sample geometry was used in this study (Fig. 1). Both the visible (532 nm) and tunable infrared (IR) beams were spatially and temporally overlapped onto the prism surface using two CaF2 lenses. A right-angled CaF2 prism substrate was placed on a three-axis translational stage: both positions on the xy plane and the height of the sample can be fine-tuned. The optical microscopic system was positioned above the prism substrate to allow visual monitoring of the sample and the laser spot (for SFG signal detection) in situ. A 40× objective and telescope were used to magnify the image onto a CCD camera. While keeping the optical microscope stationary, the three-axis translational stage mentioned above allowed full freedom to move the sample to find an ideal position for data collection. Using AFM, we determined the location of a monolayer of MoS2 with the help of neighboring thick multilayered MoS2 regions (Fig. 1). Such a location of a monolayer MoS2 region could be identified using the microscope-SFG with the help of the multilayered MoS2 regions. Then both the visible and infrared beams were focused onto this region to collect SFG spectra (Fig. 1). Structural information such as the molecular orientation of surface peptides on a single layer of MoS2 could then be measured via SFG.

Results and discussion

The sequence of a native cecropin–melittin hybrid peptide is shown in Fig. 2, where charged, hydroxyl group-containing, hydrocarbon side chain-containing, or aromatic ring-containing amino acids are labeled in red (most hydrophilic), blue (hydrophilic), black (hydrophobic), and green (most hydrophobic) respectively.30
image file: c7sc04884j-f2.tif
Fig. 2 Primary sequence (top) and SFG spectra collected from the interface between MoS2 and solutions (bottom) of the native cecropin–melittin hybrid peptide (a), mutant A (b), mutant B (c) and mutant C (d).

SFG ssp (s-polarized signal, s-polarized input visible, p-polarized input IR beams) and ppp spectra were collected from the single layer MoS2/hybrid peptide solution interface (Fig. 2a). Because no SFG signal could be detected from the bare CaF2/peptide solution interface (not shown), such signals must be due to the peptides on MoS2. Both SFG spectra exhibit a distinct amide I peak at 1650 cm−1, indicating that the hybrid peptide adopts an alpha-helical secondary structure on the MoS2 surface, with a non-parallel orientation. According to the ssp and ppp SFG amide I spectra, the orientation of the adsorbed hybrid peptide on MoS2 was determined to be 15 to 25 degrees for the alpha helix vs. the surface normal using the method published previously (Fig. 3).29 More details about the orientation determination can be found in the ESI.


image file: c7sc04884j-f3.tif
Fig. 3 Dependence of the tilt angle on the measured SFG signal strength χppp/χssp ratio for several different lengths of alpha-helical peptide (17–21 residues).

To better understand the interaction that this cecropin–melittin hybrid peptide has with MoS2, we performed molecular dynamics simulations (see details about the simulation methods in the ESI). Simulation results showed that the C-terminus of this peptide readily interacts with MoS2 and the remaining residues that are solvent accessible are at a calculated tilt angle of 20.9° from the surface normal (Fig. 4), agreeing with the experimental data quite well.


image file: c7sc04884j-f4.tif
Fig. 4 Simulation results of cecropin–melittin hybrid peptide (a), mutant A (b), mutant B (c) and mutant C (d) on an MoS2 surface.

A cecropin–melittin hybrid peptide has nine amino acid residues in the C-terminus region including one aromatic group-containing residue, five non-aromatic hydrophobic groups, and three hydroxyl-containing hydrophilic residues. The N-terminus region of the cecropin–melittin hybrid peptide has two aromatic-containing amino acids, three hydrophobic (non-aromatic-containing) residues, and four charged residues. The N-terminus has one more aromatic functionality-containing residue. If the aromatic group-containing amino acid played the dominant role in surface–peptide interaction as previously reported for graphene,13 the peptide should interact with the MoS2 surface with its N-terminus. But this was not what was observed in our molecular dynamics simulations: our simulation data indicate that the C-terminus interacts with the MoS2 surface. We therefore believe that the aromatic amino acid/surface interaction does not play the major role in the peptide/MoS2 interaction. Instead, the general hydrophobic interactions play the major role: the N-terminus is more hydrophilic because of its more charged groups, and therefore prefers to stay in the aqueous environment rather than on the surface. The C-terminus overall has more hydrophobic groups, which leads to the adsorption of the C-terminus on the surface.

To further understand the peptide–MoS2 physico-adsorption process, we designed three cecropin–melittin hybrid peptide mutants (Fig. 2) and studied their interactions with the MoS2 surface. For all three mutants, only the N-terminus of the peptide was modified, which was previously identified as being primarily driven into solution for MoS2 interactions. Mutant A has one extra aromatic residue at the N-terminus. The goal of using this mutant was to examine whether one additional aromatic residue could increase the interaction with MoS2 in order to change the peptide orientation to a lying-down pose, as previously observed in peptide-graphene interactions.13 SFG amide I signals were successfully detected from mutant A on the MoS2 surface (Fig. 2b), indicating a nonparallel pose in the α-helical conformation, which matched the MD simulation data (Fig. 4b). The simulation results again indicated that the C-terminus binds to the MoS2 surface, while the N-terminus points away from the MoS2 surface into the solution. Both the SFG experimental ratio and the simulation data showed an almost identical orientation of mutant A compared to the native hybrid peptide, showing no strong interaction between the mutant A N-terminus (with one extra aromatic residue) and MoS2. Indeed, we found through both SFG experiments and MD simulations that even with two additional aromatic side chain-containing amino acids on the N-terminus (mutant A2), the mutant A2 could still adopt a tilting pose on MoS2 without lying down (Fig. S2).

The above study on mutant A indicated that it is likely that the aromatic amino acid–MoS2 interaction is not stronger than the non-aromatic amino acid–MoS2 interaction. We wanted to know whether this is true vice versa and see whether the replacement of the aromatic amino acids with non-aromatic hydrophobic residues affects the peptide/MoS2 interaction. Therefore, the aromatic residues were all mutated to non-aromatic hydrophobic groups near the N-terminus in mutant B. SFG spectra were successfully collected from mutant B on MoS2 (Fig. 2c); its orientation was measured to be 15° to 25° versus the surface normal, similar to that deduced from the MD simulation results (α-helix with a tilt angle of 29.7°) and also similar to the case of the wild-type peptide presented above. The similar structure of mutant B on MoS2 to that of the wild-type hybrid indicated that the amino acids with non-aromatic functional groups do not interact with the MoS2 surface to a greater extent than the aromatic hydrophobic amino acids.

We then studied the effect of charged amino acids on the N-terminus by replacing charged residues with serine (mutant C). If the hydrophilic hydroxyl groups interact with water less favorably than the charged residues, mutant C might lie down on the surface. Indeed, no discernable SFG amide I signal could be detected from the interface between MoS2 and the mutant C solution. The absence of a SFG signal could be because (1) no peptide was adsorbed onto the MoS2 surface, or (2) all adsorbed peptides were lying down. To differentiate between these two possibilities, circular dichroism (CD) spectroscopy, sensitive to only secondary structure and not orientation, was used (ESI). CD data demonstrated that mutant C was present on the MoS2 surface with an alpha helical secondary structure (Fig. S3). The above finding was also validated by molecular dynamics simulation (Fig. 4d).

Conclusion

In conclusion, we applied a unique analytical platform to combine an optical microscope with an SFG spectrometer to study peptide interactions that occur on heterogeneous MoS2 surfaces. This study elucidated the detailed molecular interactions between a cecropin–melittin hybrid peptide and a MoS2 surface. We found that the aromatic amino acids do not have a substantial effect on peptides interacting with the MoS2 surface. With three rationally designed peptide mutants (mutants A, B and C), more details about the peptide interactions on MoS2 were deduced. It was found that the charged groups in the N-terminus region are needed for the peptide to interact more favorably with the aqueous environment and ensure a “standing-up” peptide pose on MoS2. SFG experimental results and MD simulation results showed excellent agreement, validating the results obtained in this research: the wild-type hybrid peptide, mutant A, and mutant B were all able to interact favorably with MoS2 via their C-terminus while tilting at around 20° and being solvent accessible. Mutant C, on the other hand, lay down on the MoS2 surface completely. This fundamental research on the hybrid peptide/MoS2 interactions lay a foundation for future investigations on the interactions between other peptides and MoS2, providing insight into the rational design of MoS2 based biosensors using peptides and proteins. The different mechanisms of the peptide–MoS2 interactions elucidated in this research, compared to the previously reported peptide–graphene interactions, clearly indicated that it is necessary to study peptide–2D material interactions when different 2D materials were chosen for sensor design. In biosensing applications, it is necessary to control the substrate surface–active biosensing unit interactions to optimize the sensing selectivity and sensitivity. This research also further demonstrated the power of using a microscope-SFG system to study heterogeneous surfaces and interfaces.

Conflicts of interest

There are no conflicts to declare.

Acknowledgements

This research is supported by the National Science Foundation (CHE-1505385 for Z. C. and CHE-1506273 for C. B.) and the University of Michigan.

Notes and references

  1. A. K. Geim and K. S. Novoselov, The rise of graphene, Nat. Mater., 2007, 6, 183–191 CrossRef CAS PubMed.
  2. Y. Zhang, Y.-W. Tan, H. L. Stormer and P. Kim, Experimental observation of the quantum Hall effect and Berry’s phase in graphene, Nature, 2005, 438, 201–204 CrossRef CAS PubMed.
  3. F. K. Perkins, A. L. Friedman, E. Cobas, P. Campbell, G. Jernigan and B. T. Jonker, Chemical vapor sensing with monolayer MoS2, Nano Lett., 2013, 13, 668–673 CrossRef CAS PubMed.
  4. D. Sarkar, W. Liu, X. Xie, A. C. Anselmo, S. Mitragotri and K. Banerjee, MoS2 field-effect transistor for next-generation label-free biosensors, ACS Nano, 2014, 8, 3992–4003 CrossRef CAS PubMed.
  5. C. Zhu, Z. Zeng, H. Li, F. Li, C. Fan and H. Zhang, Single-layer MoS2-based nanoprobes for homogeneous detection of biomolecules, J. Am. Chem. Soc., 2013, 135, 5998–6001 CrossRef CAS PubMed.
  6. H. Nam, B.-R. Oh, M. Chen, S. Wi, D. Li, K. Kurabayashi and X. Liang, Fabrication and comparison of MoS2 and WSe2 field-effect transistor biosensors, J. Vac. Sci. Technol., B: Nanotechnol. Microelectron.: Mater., Process., Meas., Phenom., 2015, 33, 06FG01 Search PubMed.
  7. C. H. Naylor, N. Kybert, C. Schneier, J. Xi, G. Romero, J. Saven, R. Liu and A. T. C. Johnson, Scalable Production of Molybdenum Disulfide Based Biosensors, ACS Nano, 2016, 10, 6173–6179 CrossRef CAS PubMed.
  8. G. Guan, S. Zhang, S. Liu, Y. Cai, M. Low, C. P. Teng, I. Y. Phang, Y. Cheng, K. L. Duei, B. M. Srinivasan and Y. Zheng, Protein induces layer-by-layer exfoliation of transition metal dichalcogenides, J. Am. Chem. Soc., 2015, 137, 6152–6155 CrossRef CAS PubMed.
  9. J. Paredes and S. Villar-Rodil, Biomolecule-assisted exfoliation and dispersion of graphene and other two-dimensional materials: a review of recent progress and applications, Nanoscale, 2016, 8, 15389–15413 RSC.
  10. H. Fan, D. Zhao, Y. Li and J. Zhou, Lysozyme orientation and conformation on MoS2 surface: Insights from molecular simulations, Biointerphases, 2017, 12, 02D416 CrossRef PubMed.
  11. Z. Gu, Z. Yang, S.-g. Kang, J. R. Yang, J. Luo and R. Zhou, Robust denaturation of villin headpiece by MoS2 nanosheet: Potential molecular origin of the nanotoxicity, Sci. Rep., 2016, 6, 28252 CrossRef CAS PubMed.
  12. Y. Ling, Z. Gu, S.-g. Kang, J. Luo and R. Zhou, Structural damage of a β-sheet protein upon adsorption onto molybdenum disulfide nanotubes, J. Phys. Chem. C, 2016, 120, 6796–6803 CAS.
  13. X. Zou, S. Wei, J. Jasensky, M. Xiao, Q. Wang, C. L. Brooks III and Z. Chen, Molecular Interactions between Graphene and Biological Molecules, J. Am. Chem. Soc., 2017, 139, 1928–1936 CrossRef CAS PubMed.
  14. C. Zhang, J. Jasensky, C. Leng, C. Del Grosso, G. D. Smith, J. J. Wilker and Z. Chen, Sum frequency generation vibrational spectroscopic studies on buried heterogeneous biointerfaces, Opt. Lett., 2014, 39, 2715–2718 CrossRef CAS PubMed.
  15. Z. Chen, Y. Shen and G. A. Somorjai, Studies of polymer surfaces by sum frequency generation vibrational spectroscopy, Annu. Rev. Phys. Chem, 2002, 53, 437–465 CrossRef CAS PubMed.
  16. Y. Shen, Surface properties probed by second-harmonic and sum-frequency generation, Nature, 1989, 337, 519–525 CrossRef CAS.
  17. S. Y. Jung, S. M. Lim, F. Albertorio, G. Kim, M. C. Gurau, R. D. Yang, M. A. Holden and P. S. Cremer, The Vroman effect: a molecular level description of fibrinogen displacement, J. Am. Chem. Soc., 2003, 125, 12782–12786 CrossRef CAS PubMed.
  18. H. Lutz, V. Jaeger, L. Schmüser, M. Bonn, J. Pfaendtner and T. Weidner, The Structure of the Diatom Silaffin Peptide R5 within Freestanding Two-Dimensional Biosilica Sheets, Angew. Chem., Int. Ed., 2017, 56, 8277–8280 CrossRef CAS PubMed.
  19. J.-S. Samson, R. Scheu, N. Smolentsev, S. W. Rick and S. Roke, Sum frequency spectroscopy of the hydrophobic nanodroplet/water interface: Absence of hydroxyl ion and dangling OH bond signatures, Chem. Phys. Lett., 2014, 615, 124–131 CrossRef CAS.
  20. S. Ye, J. Tan, B. Zhang and Y. Luo, Ultrafast Vibrational Dynamics of Membrane-Bound Peptides at the Lipid Bilayer/Water Interface, Angew. Chem., Int. Ed., 2017, 56, 12977–12981 CrossRef PubMed.
  21. X. Liu, C. Leng, L. Yu, K. He, L. J. Brown, Z. Chen, J. Cho and D. Wang, Ion-Specific Oil Repellency of Polyelectrolyte Multilayers in Water: Molecular Insights into the Hydrophilicity of Charged Surfaces, Angew. Chem., Int. Ed., 2015, 54, 4851–4856 CrossRef CAS PubMed.
  22. B. Ding, J. Jasensky, Y. Li and Z. Chen, Engineering and Characterization of Peptides and Proteins at Surfaces and Interfaces: A Case Study in Surface-Sensitive Vibrational Spectroscopy, Acc. Chem. Res., 2016, 49, 1149–1157 CrossRef CAS PubMed.
  23. Y. Li, X. Zhang, J. Myers, N. L. Abbott and Z. Chen, Room temperature freezing and orientational control of surface-immobilized peptides in air, Chem. Commun., 2015, 51, 11015–11018 RSC.
  24. T. Weidner, J. S. Apte, L. J. Gamble and D. G. Castner, Probing the orientation and conformation of α-helix and β-strand model peptides on self-assembled monolayers using sum frequency generation and NEXAFS spectroscopy, Langmuir, 2009, 26, 3433–3440 CrossRef PubMed.
  25. D. Schach, C. Globisch, S. J. Roeters, S. Woutersen, A. Fuchs, C. K. Weiss, E. H. Backus, K. Landfester, M. Bonn, C. Peter and T. Weidner, Sticky water surfaces: Helix–coil transitions suppressed in a cell-penetrating peptide at the air-water interface, J. Chem. Phys., 2014, 141, 22D517 CrossRef PubMed.
  26. E. C. Yan, L. Fu, Z. Wang and W. Liu, Biological macromolecules at interfaces probed by chiral vibrational sum frequency generation spectroscopy, Chem. Rev., 2014, 114, 8471–8498 CrossRef CAS PubMed.
  27. L. Schmueser, S. J. Roeters, H. Lutz, S. Woutersen, M. Bonn and T. Weidner, Determination of Absolute Orientation of Protein α-Helices at Interfaces using Phase Resolved SFG Spectroscopy, J. Phys. Chem. Lett., 2017, 8, 3101–3105 CrossRef CAS PubMed.
  28. A. G. De Beer and S. Roke, What interactions can distort the orientational distribution of interfacial water molecules as probed by second harmonic and sum frequency generation?, J. Chem. Phys., 2016, 145, 044705 CrossRef PubMed.
  29. K. T. Nguyen, S. V. Le Clair, S. Ye and Z. Chen, Orientation determination of protein helical secondary structures using linear and nonlinear vibrational spectroscopy, J. Phys. Chem. B, 2009, 113, 12169–12180 CrossRef CAS PubMed.
  30. O. D. Monera, T. J. Sereda, N. E. Zhou, C. M. Kay and R. S. Hodges, Relationship of sidechain hydrophobicity and α-helical propensity on the stability of the single-stranded amphipathic α-helix, J. Pept. Sci., 1995, 1, 319–329 CrossRef CAS PubMed.

Footnote

Electronic supplementary information (ESI) available: SFG data analysis methods, spectral fitting parameters, additional spectra, CD spectrum, and details about MD simulation methods. See DOI: 10.1039/c7sc04884j

This journal is © The Royal Society of Chemistry 2018