Jannis Weinacker, Bikash Kumar Bhandari, Alba Viejo Rodriguez, Charlotte West, Francesco De Angelis, Francesco Tantussi, Nicolò Maccaferri, Nick Goldman, Martin Wegener
{"title":"使用紧凑型3D打印微光学元件从低强度氨基酸拉曼信号中识别蛋白质的协议","authors":"Jannis Weinacker, Bikash Kumar Bhandari, Alba Viejo Rodriguez, Charlotte West, Francesco De Angelis, Francesco Tantussi, Nicolò Maccaferri, Nick Goldman, Martin Wegener","doi":"10.1002/admt.202401876","DOIUrl":null,"url":null,"abstract":"<p>When performing optical high-speed single-molecule spectroscopy and identification, low signal intensities pose a challenge. Fortunately, for many applications, the number of possible molecules in the specimen is small or limited. For such cases, a protocol is presented that uses only a small number of very sensitive hence expensive detectors. The protocol starts with optimizing spectral regions, one per detector, so that different molecules become best distinguishable. Experimentally, the spectral regions are extracted from the continuous spectrum using a custom-made micro-optical element. In the ray-optics picture, it guides all rays in a spectral region onto the entrance of an optical fiber connected to one detector. The shape of the micro-optical element is derived by applying Snell's law to the given geometrical boundary conditions. A proof-of-concept measurement using a dedicated demonstrator refractive optical element in combination with a continuous white-light source is performed. Indeed, the element selects the correct spectral regions and couples the light into the correct fibers. For the example of the identification of single amino acids in a protein, the protocol leads to a higher correct identification rate. Therefore, this protocol is useful for such protein identification experiments as performed in the EU project ProID.</p>","PeriodicalId":7292,"journal":{"name":"Advanced Materials Technologies","volume":"10 9","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admt.202401876","citationCount":"0","resultStr":"{\"title\":\"A Protocol Using Compact 3D Printed Micro-Optical Elements for Protein Identification from Low-Intensity Amino-Acid Raman Signals\",\"authors\":\"Jannis Weinacker, Bikash Kumar Bhandari, Alba Viejo Rodriguez, Charlotte West, Francesco De Angelis, Francesco Tantussi, Nicolò Maccaferri, Nick Goldman, Martin Wegener\",\"doi\":\"10.1002/admt.202401876\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>When performing optical high-speed single-molecule spectroscopy and identification, low signal intensities pose a challenge. Fortunately, for many applications, the number of possible molecules in the specimen is small or limited. For such cases, a protocol is presented that uses only a small number of very sensitive hence expensive detectors. The protocol starts with optimizing spectral regions, one per detector, so that different molecules become best distinguishable. Experimentally, the spectral regions are extracted from the continuous spectrum using a custom-made micro-optical element. In the ray-optics picture, it guides all rays in a spectral region onto the entrance of an optical fiber connected to one detector. The shape of the micro-optical element is derived by applying Snell's law to the given geometrical boundary conditions. A proof-of-concept measurement using a dedicated demonstrator refractive optical element in combination with a continuous white-light source is performed. Indeed, the element selects the correct spectral regions and couples the light into the correct fibers. For the example of the identification of single amino acids in a protein, the protocol leads to a higher correct identification rate. 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A Protocol Using Compact 3D Printed Micro-Optical Elements for Protein Identification from Low-Intensity Amino-Acid Raman Signals
When performing optical high-speed single-molecule spectroscopy and identification, low signal intensities pose a challenge. Fortunately, for many applications, the number of possible molecules in the specimen is small or limited. For such cases, a protocol is presented that uses only a small number of very sensitive hence expensive detectors. The protocol starts with optimizing spectral regions, one per detector, so that different molecules become best distinguishable. Experimentally, the spectral regions are extracted from the continuous spectrum using a custom-made micro-optical element. In the ray-optics picture, it guides all rays in a spectral region onto the entrance of an optical fiber connected to one detector. The shape of the micro-optical element is derived by applying Snell's law to the given geometrical boundary conditions. A proof-of-concept measurement using a dedicated demonstrator refractive optical element in combination with a continuous white-light source is performed. Indeed, the element selects the correct spectral regions and couples the light into the correct fibers. For the example of the identification of single amino acids in a protein, the protocol leads to a higher correct identification rate. Therefore, this protocol is useful for such protein identification experiments as performed in the EU project ProID.
期刊介绍:
Advanced Materials Technologies Advanced Materials Technologies is the new home for all technology-related materials applications research, with particular focus on advanced device design, fabrication and integration, as well as new technologies based on novel materials. It bridges the gap between fundamental laboratory research and industry.