Proline optical probe and preparation method and application thereof
An optical probe, proline technology, applied in the field of optical probes, can solve the problems of time-consuming, cell fragmentation, etc., and achieve the effects of easy maturation, good specificity, and large dynamic changes in fluorescence
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[0071] In an exemplary embodiment, the B1-A-B2 type optical probe of the present invention may be Atu2422 fused to cpYFP at site 121 / 122 and having a compound selected from the group consisting of F77L, A100G, D121E, D121S, D121T, D121V, D226E, D226N and Probes formed upon mutation of Y275F are shown in SEQ ID NOs: 16-24.
[0072] The optical probe provided by the present invention comprises any one of the amino acid sequences SEQ ID NO: 10-24 or a variant thereof. In one embodiment, the optical probe provided by the present invention comprises 35%, 40%, 50%, 60%, 70%, 80%, 85%, 90% of the amino acid sequence SEQ ID NO: 10-24. Sequences with %, 95%, 99% sequence identity. In a preferred embodiment, the optical probe provided by the present invention comprises a sequence substantially similar or identical to any of the amino acid sequences SEQ ID NOs: 10-24. In a more preferred embodiment, the optical probe provided by the present invention comprises or consists of SEQ ID NO:...
Embodiment 1
[0163] Example 1: Proline-Binding Protein Particles
[0164] The proline-binding protein (here Atu2422) gene in Agrobacterium tumefaciens was amplified by PCR, and the PCR product was recovered after gel electrophoresis and digested with BamHI and EcoRI, while the pRSETb vector was subjected to corresponding double digestion. After ligation with T4 DNA ligase, MachI was transformed with the product, and the transformed MachI was spread on an LB plate (100 ug / mL of ampicillin) and cultured at 37°C overnight. After plasmid extraction of the growing MachI transformants, PCR identification was performed. After the positive plasmids were sequenced correctly, the subsequent plasmid construction was carried out.
Embodiment 2
[0165] Example 2: Expression and detection of cpYFP optical probes at different fusion sites
[0166]In this example, the following sites were selected to fuse cpYFP based on pRSETb-Atu2422 to obtain the corresponding pRSETb-Atu2422-cpYFP plasmids: 117 / 118, 117 / 119, 117 / 120, 117 / 121, 118 / 119, 118 / 120, 118 / 121, 119 / 120, 119 / 121, 120 / 121, 120 / 122, 120 / 123, 121 / 122, 121 / 123, 122 / 123, 249 / 250, 249 / 251, 249 / 252, 249 / 253, 249 / 254, 249 / 255, 249 / 256, 249 / 257, 249 / 258, 249 / 259, 250 / 251, 250 / 252, 250 / 253, 250 / 254, 250 / 255, 250 / 256, 250 / 257, 250 / 258, 250 / 259, 251 / 252, 251 / 253, 251 / 254, 251 / 255, 251 / 256, 251 / 257, 251 / 258, 251 / 259, 252 / 253, 252 / 254, 252 / 255, 252 / 256, 252 / 257, 252 / 258, 252 / 259, 253 / 254, 253 / 255, 253 / 256, 253 / 257, 253 / 258, 253 / 259, 254 / 255, 254 / 256, 254 / 257, 254 / 258, 254 / 259, 255 / 256, 255 / 257, 255 / 258, 255 / 259, 256 / 257, 256 / 258, 256 / 259, 257 / 258, 257 / 259, 258 / 259, 323 / 330, 324 / 330, 325 / 330, 326 / 327, 326 / 328, 326 / 329, 326 / 330, 327 / 328, 327 / 329, 327 / 330, 328 / 329, 328 / 3...
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