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Sensors for Proteolytic Activity Visualization and Their Application in Animal Models of Human Diseases
Various sensors designed for optical and photo(opto)acoustic imaging in living systems are becoming essential components of basic and applied biomedical research. Some of them including those developed for determining enzyme activity in vivo are becoming commercially available. These sensors can be...
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Published in: | Biochemistry (Moscow) 2019, Vol.84 (Suppl 1), p.1-18 |
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container_title | Biochemistry (Moscow) |
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description | Various sensors designed for optical and photo(opto)acoustic imaging in living systems are becoming essential components of basic and applied biomedical research. Some of them including those developed for determining enzyme activity
in vivo
are becoming commercially available. These sensors can be used for various fluorescent signal detection methods: from whole body tomography to endoscopy with miniature cameras. Sensor molecules including enzyme-cleavable macromolecules carrying multiple quenched near-infrared fluorophores are able to deliver their payload
in vivo
and have long circulation time in bloodstream enabling detection of enzyme activity for extended periods of time at low doses of these sensors. In the future, more effective “activated” probes are expected to become available with optimized sensitivity to enzymatic activity, spectral characteristics suitable for intraoperative imaging of surgical field, biocompatibility and lack of immunogenicity and toxicity. New
in vivo
optical imaging methods such as the fluorescence lifetime and photo(opto)acoustic imaging will contribute to early diagnosis of human diseases. The use of sensors for
in vivo
optical imaging will include more extensive preclinical applications of experimental therapies. At the same time, the ongoing development and improvement of optical signal detectors as well as the availability of biologically inert and highly specific fluorescent probes will further contribute to the introduction of fluorescence imaging into the clinic. |
doi_str_mv | 10.1134/S0006297919140013 |
format | article |
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in vivo
are becoming commercially available. These sensors can be used for various fluorescent signal detection methods: from whole body tomography to endoscopy with miniature cameras. Sensor molecules including enzyme-cleavable macromolecules carrying multiple quenched near-infrared fluorophores are able to deliver their payload
in vivo
and have long circulation time in bloodstream enabling detection of enzyme activity for extended periods of time at low doses of these sensors. In the future, more effective “activated” probes are expected to become available with optimized sensitivity to enzymatic activity, spectral characteristics suitable for intraoperative imaging of surgical field, biocompatibility and lack of immunogenicity and toxicity. New
in vivo
optical imaging methods such as the fluorescence lifetime and photo(opto)acoustic imaging will contribute to early diagnosis of human diseases. The use of sensors for
in vivo
optical imaging will include more extensive preclinical applications of experimental therapies. At the same time, the ongoing development and improvement of optical signal detectors as well as the availability of biologically inert and highly specific fluorescent probes will further contribute to the introduction of fluorescence imaging into the clinic.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1134/S0006297919140013</identifier><identifier>PMID: 31213192</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Acoustic imaging ; Amino acids ; Animal diseases ; Animal models ; Animals ; Biochemistry ; Biocompatibility ; Biomedical and Life Sciences ; Biomedical materials ; Biomedicine ; Bioorganic Chemistry ; Biosensing Techniques - methods ; Cameras ; Chemical compounds ; Detectors ; Disease Models, Animal ; Diseases ; Early Diagnosis ; Endoscopy ; Enzymatic activity ; Enzyme activity ; Enzymes ; Fluorescence ; Fluorescent Dyes - chemistry ; Fluorescent indicators ; Fluorophores ; Humans ; Immunogenicity ; In vivo methods and tests ; Life Sciences ; Macromolecules ; Medical imaging ; Medical research ; Medicine, Experimental ; Methylene blue ; Microbiology ; Optical communication ; Optical Imaging - methods ; Peptide Hydrolases - metabolism ; Probes ; Proteolysis ; Review ; Sensors ; Signal detection ; Signal detectors ; Spectral sensitivity ; Toxicity</subject><ispartof>Biochemistry (Moscow), 2019, Vol.84 (Suppl 1), p.1-18</ispartof><rights>Pleiades Publishing, Ltd. 2019</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Biochemistry (Moscow) is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-c0a0bb135743fbbbb029eb7004c0f7cecffc010da7407189bfce39f54fe4fa2d3</citedby><cites>FETCH-LOGICAL-c439t-c0a0bb135743fbbbb029eb7004c0f7cecffc010da7407189bfce39f54fe4fa2d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31213192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bogdanov, A. A.</creatorcontrib><creatorcontrib>Solovyev, I. D.</creatorcontrib><creatorcontrib>Savitsky, A. P.</creatorcontrib><title>Sensors for Proteolytic Activity Visualization and Their Application in Animal Models of Human Diseases</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry Moscow</addtitle><addtitle>Biochemistry (Mosc)</addtitle><description>Various sensors designed for optical and photo(opto)acoustic imaging in living systems are becoming essential components of basic and applied biomedical research. Some of them including those developed for determining enzyme activity
in vivo
are becoming commercially available. These sensors can be used for various fluorescent signal detection methods: from whole body tomography to endoscopy with miniature cameras. Sensor molecules including enzyme-cleavable macromolecules carrying multiple quenched near-infrared fluorophores are able to deliver their payload
in vivo
and have long circulation time in bloodstream enabling detection of enzyme activity for extended periods of time at low doses of these sensors. In the future, more effective “activated” probes are expected to become available with optimized sensitivity to enzymatic activity, spectral characteristics suitable for intraoperative imaging of surgical field, biocompatibility and lack of immunogenicity and toxicity. New
in vivo
optical imaging methods such as the fluorescence lifetime and photo(opto)acoustic imaging will contribute to early diagnosis of human diseases. The use of sensors for
in vivo
optical imaging will include more extensive preclinical applications of experimental therapies. At the same time, the ongoing development and improvement of optical signal detectors as well as the availability of biologically inert and highly specific fluorescent probes will further contribute to the introduction of fluorescence imaging into the clinic.</description><subject>Acoustic imaging</subject><subject>Amino acids</subject><subject>Animal diseases</subject><subject>Animal models</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biocompatibility</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical materials</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>Biosensing Techniques - methods</subject><subject>Cameras</subject><subject>Chemical compounds</subject><subject>Detectors</subject><subject>Disease Models, Animal</subject><subject>Diseases</subject><subject>Early Diagnosis</subject><subject>Endoscopy</subject><subject>Enzymatic activity</subject><subject>Enzyme activity</subject><subject>Enzymes</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent indicators</subject><subject>Fluorophores</subject><subject>Humans</subject><subject>Immunogenicity</subject><subject>In vivo methods and tests</subject><subject>Life Sciences</subject><subject>Macromolecules</subject><subject>Medical imaging</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Methylene blue</subject><subject>Microbiology</subject><subject>Optical communication</subject><subject>Optical Imaging - methods</subject><subject>Peptide Hydrolases - metabolism</subject><subject>Probes</subject><subject>Proteolysis</subject><subject>Review</subject><subject>Sensors</subject><subject>Signal detection</subject><subject>Signal detectors</subject><subject>Spectral sensitivity</subject><subject>Toxicity</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kU1v1DAQhi0EokvhB3BBlrhwSZmxnWZ9jAq0SEUgtXCNHGe8uErsxU6Qll9fr7ZQ8WUfrJl53lfjGcaeI5wgSvX6CgBOhW40alQAKB-wFZ7CupKg4CFb7cvVvn7EnuR8U0IBWj5mRxIFStRixTZXFHJMmbuY-KcUZ4rjbvaWt3b23_284198Xszof5jZx8BNGPj1V_KJt9vt6O0h6wNvg5_MyD_EgcbMo-MXy2QCf-MzmUz5KXvkzJjp2d17zD6_e3t9dlFdfjx_f9ZeVlZJPVcWDPQ9yrpR0vXlgNDUNwDKgmssWecsIAymUdDgWvfOktSuVo6UM2KQx-zVwXeb4reF8txNPlsaRxMoLrkTQkmli2Fd0Jd_oDdxSaF0VyjEGstc4Z7amJE6H1yck7F7065dgyrjrsW6UCf_oModaPI2BnK-5H8T4EFgU8w5keu2qQww7TqEbr_c7q_lFs2Lu4aXfqLhl-LnNgsgDkAupbChdP-j_7veArKTrOY</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Bogdanov, A. A.</creator><creator>Solovyev, I. D.</creator><creator>Savitsky, A. P.</creator><general>Pleiades Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>2019</creationdate><title>Sensors for Proteolytic Activity Visualization and Their Application in Animal Models of Human Diseases</title><author>Bogdanov, A. A. ; Solovyev, I. D. ; Savitsky, A. P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-c0a0bb135743fbbbb029eb7004c0f7cecffc010da7407189bfce39f54fe4fa2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acoustic imaging</topic><topic>Amino acids</topic><topic>Animal diseases</topic><topic>Animal models</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biocompatibility</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical materials</topic><topic>Biomedicine</topic><topic>Bioorganic Chemistry</topic><topic>Biosensing Techniques - methods</topic><topic>Cameras</topic><topic>Chemical compounds</topic><topic>Detectors</topic><topic>Disease Models, Animal</topic><topic>Diseases</topic><topic>Early Diagnosis</topic><topic>Endoscopy</topic><topic>Enzymatic activity</topic><topic>Enzyme activity</topic><topic>Enzymes</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent indicators</topic><topic>Fluorophores</topic><topic>Humans</topic><topic>Immunogenicity</topic><topic>In vivo methods and tests</topic><topic>Life Sciences</topic><topic>Macromolecules</topic><topic>Medical imaging</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Methylene blue</topic><topic>Microbiology</topic><topic>Optical communication</topic><topic>Optical Imaging - methods</topic><topic>Peptide Hydrolases - metabolism</topic><topic>Probes</topic><topic>Proteolysis</topic><topic>Review</topic><topic>Sensors</topic><topic>Signal detection</topic><topic>Signal detectors</topic><topic>Spectral sensitivity</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bogdanov, A. 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A.</au><au>Solovyev, I. D.</au><au>Savitsky, A. P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sensors for Proteolytic Activity Visualization and Their Application in Animal Models of Human Diseases</atitle><jtitle>Biochemistry (Moscow)</jtitle><stitle>Biochemistry Moscow</stitle><addtitle>Biochemistry (Mosc)</addtitle><date>2019</date><risdate>2019</risdate><volume>84</volume><issue>Suppl 1</issue><spage>1</spage><epage>18</epage><pages>1-18</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>Various sensors designed for optical and photo(opto)acoustic imaging in living systems are becoming essential components of basic and applied biomedical research. Some of them including those developed for determining enzyme activity
in vivo
are becoming commercially available. These sensors can be used for various fluorescent signal detection methods: from whole body tomography to endoscopy with miniature cameras. Sensor molecules including enzyme-cleavable macromolecules carrying multiple quenched near-infrared fluorophores are able to deliver their payload
in vivo
and have long circulation time in bloodstream enabling detection of enzyme activity for extended periods of time at low doses of these sensors. In the future, more effective “activated” probes are expected to become available with optimized sensitivity to enzymatic activity, spectral characteristics suitable for intraoperative imaging of surgical field, biocompatibility and lack of immunogenicity and toxicity. New
in vivo
optical imaging methods such as the fluorescence lifetime and photo(opto)acoustic imaging will contribute to early diagnosis of human diseases. The use of sensors for
in vivo
optical imaging will include more extensive preclinical applications of experimental therapies. At the same time, the ongoing development and improvement of optical signal detectors as well as the availability of biologically inert and highly specific fluorescent probes will further contribute to the introduction of fluorescence imaging into the clinic.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><pmid>31213192</pmid><doi>10.1134/S0006297919140013</doi><tpages>18</tpages></addata></record> |
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source | Springer Nature |
subjects | Acoustic imaging Amino acids Animal diseases Animal models Animals Biochemistry Biocompatibility Biomedical and Life Sciences Biomedical materials Biomedicine Bioorganic Chemistry Biosensing Techniques - methods Cameras Chemical compounds Detectors Disease Models, Animal Diseases Early Diagnosis Endoscopy Enzymatic activity Enzyme activity Enzymes Fluorescence Fluorescent Dyes - chemistry Fluorescent indicators Fluorophores Humans Immunogenicity In vivo methods and tests Life Sciences Macromolecules Medical imaging Medical research Medicine, Experimental Methylene blue Microbiology Optical communication Optical Imaging - methods Peptide Hydrolases - metabolism Probes Proteolysis Review Sensors Signal detection Signal detectors Spectral sensitivity Toxicity |
title | Sensors for Proteolytic Activity Visualization and Their Application in Animal Models of Human Diseases |
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