It is generally accepted that the bound states in the continuum (BICs) are usually realized in a one-dimensional system by the TM-polarized light incident at Brewster's angle. However, the optimal BICs can be achieved only under specific incident light and at a specific polarization incident angle, which poses challenges to its experimental implementation. Serving this purpose, we design a system composed of an anisotropic material (AM) embedded in one-dimensional photonic crystals (1D-PhCs), demonstrating that both TE and TM waves can realize BICs. Moreover, the existence of BICs does not hinge on the specific angle of the incident light. In contrast to the traditional methods of creation system symmetry to achieve symmetry-protected BICs (SP-BICs), we use the 1D-PhC to confine the TE or TM wave in different frequencies first as a form of cavity (localized) mode and rotating the optical axis of AM at a specific angle to realize the field mismatch. Besides, our system can realize Friedrich-Wintgen BICs (FW-BICs) because of the destructive interference of the radiative waves in other specific angles, which can be detected as some Fano resonance collapsing points in reflection spectra. Our results provide more flexible conditions for the realization of BICs under the TE-polarized light, making the implementation of switch Q-factor easier.
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Department of Biophysics, Molecular Biology and Bioinformatics, University College of Science, University of Calcutta, Kolkata, India.
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Key Laboratory of Medicinal and Edible Plants Resources Development of Sichuan Education Department, School of Pharmacy, Chengdu University, Chengdu 610106, China.
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Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA 99163-1062, USA; Department of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA 99163-1062, USA. Electronic address:
Sarcomere length-dependent activation (LDA) is the key cellular mechanism underlying the Frank-Starling law of the heart, in which sarcomere stretch leads to increased Ca sensitivity of myofilament and force of contraction. Despite its key role in both normal and pathological states, the precise mechanisms underlying LDA remain unclear but are thought to involve multiple interactions among sarcomere proteins, including troponin of the thin filament, myosin, titin and myosin binding protein C (MyBP-C). Our previous study with permeabilized rat cardiac fibers demonstrated that the mechanism underlying the increase in Ca sensitivity of thin filament induced by sarcomere stretch may involve sarcomere length (SL)-induced interactions between troponin and weakly bound, disordered relaxed state (DRX) myosin heads in diastole, rather than strong myosin-actin crossbridge interactions.
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Donostia International Physics Center, Paseo Manuel de Lardizábal 4, 20018 San Sebastián, Spain.
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