Vectores para la clonación y expresión de proteínas, métodos y aplicaciones de estos

Una constructo de vector disenado para recibir un anticuerpo o un fragmento de este a partir de un fagemido que comprende al menos una region de clonacion o a partir de un vector de levadura que comprende al menos una region de clonacion, o, para transferir un anticuerpo o un fragmento de este a un...

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Hauptverfasser: MAITY, Sunit, DAKSHINAMURTHY, Pravin Kumar, MALIWALAVE, Amol, GHOSH, Maloy, HALAN, Vivek, UNNIKRISHNAN, Divya, KHAN, Amir, MUNIRAJU, Yogendra Manjunath Bangalore, M, Nikitha, NAIR, Karthika, RODRIGUES, Kavitha Iyer, TIWARI, Anurag, CHATTERJEE, Sohang, PRASAD, Bhargav, CHAKRABARTY, Subhra Prakash, SRINIVASAN, Sankaranarayanan, PATEL, Shivani, RAO, Sahana Bhima, DUBEY, Ashvini Kumar, BHATTACHARJEE, Sanghamitra, KAMANAGOWDA, Veeresha, KUMAR, Santosh, NATARAJAN, Bairavabalakumar, SHARMA, Ankurina, THANIGAIVEL, Aswini, SHARMA, Rashmi, SHENOY, Bharath Ravindra, HORA, Anuradha, MUKUNDA, Pavithra, MURUGESAN, Sathyabalan
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creator MAITY, Sunit
DAKSHINAMURTHY, Pravin Kumar
MALIWALAVE, Amol
GHOSH, Maloy
HALAN, Vivek
UNNIKRISHNAN, Divya
KHAN, Amir
MUNIRAJU, Yogendra Manjunath Bangalore
M, Nikitha
NAIR, Karthika
RODRIGUES, Kavitha Iyer
TIWARI, Anurag
CHATTERJEE, Sohang
PRASAD, Bhargav
CHAKRABARTY, Subhra Prakash
SRINIVASAN, Sankaranarayanan
PATEL, Shivani
RAO, Sahana Bhima
DUBEY, Ashvini Kumar
BHATTACHARJEE, Sanghamitra
KAMANAGOWDA, Veeresha
KUMAR, Santosh
NATARAJAN, Bairavabalakumar
SHARMA, Ankurina
THANIGAIVEL, Aswini
SHARMA, Rashmi
SHENOY, Bharath Ravindra
HORA, Anuradha
MUKUNDA, Pavithra
MURUGESAN, Sathyabalan
description Una constructo de vector disenado para recibir un anticuerpo o un fragmento de este a partir de un fagemido que comprende al menos una region de clonacion o a partir de un vector de levadura que comprende al menos una region de clonacion, o, para transferir un anticuerpo o un fragmento de este a un vector de levadura que comprende al menos una region de clonacion, donde dicho constructo de vector contiene un casete de expresion que comprende: al menos una secuencia lider; al menos una region de clonacion para recibir un gen que codifica un peptido o proteina que se une selectivamente a un ligando biologicamente activo; al menos una secuencia de nucleotidos que codifica la region constante de la cadena pesada de inmunoglobulina o la region constante de la cadena ligera de inmunoglobulina, o fragmentos de estas, o una combinacion de la region constante de la cadena pesada de inmunoglobulina o un fragmento de esta y la region constante de la cadena ligera de inmunoglobulina o fragmento de esta, en donde dicha region constante comprende al menos una mutacion con respecto a la region constante de una inmunoglobulina nativa o fragmentos de esta; y al menos una secuencia de etiqueta recombinante o secuencia de acido nucleico codificante de seleccion; en donde la al menos una region de clonacion del casete de expresion comprende un sitio de clonacion multiple 1 (MCS I) y un sitio de clonacion multiple 2 (MCS II), un sitio de clonacion multiple 1 (MCS I) solo o un sitio de clonacion multiple 2 (MCS II) solo, y en donde MCS I comprende una combinacion de los sitios de restriccion NdeI y BglII y HindIII y AscI, y el MCS II comprende una combinacion de los sitios de restriccion NcoI y XbaI y NheI y NotI. The present disclosure relates to vectors for cloning and expressing genetic material including but not limiting to antibody gene or parts thereof and methods of generating said vectors. Said vectors express the antibody genes in different formats such as Fab or scFv as a part of intertransfer system, intratransfer system or direct cloning and expression in individual display systems. In particular, phage display technology is used to clone and screen potential antibody genes in phagemid which is followed by the transfer of said genes to yeast vector for further screening and identification of lead molecules against antigens. The present vectors have numerous advantages including uniquely designed inserts/expression cassettes resulting in efficient and smooth transfer
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The present disclosure relates to vectors for cloning and expressing genetic material including but not limiting to antibody gene or parts thereof and methods of generating said vectors. Said vectors express the antibody genes in different formats such as Fab or scFv as a part of intertransfer system, intratransfer system or direct cloning and expression in individual display systems. In particular, phage display technology is used to clone and screen potential antibody genes in phagemid which is followed by the transfer of said genes to yeast vector for further screening and identification of lead molecules against antigens. 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DAKSHINAMURTHY, Pravin Kumar ; MALIWALAVE, Amol ; GHOSH, Maloy ; HALAN, Vivek ; UNNIKRISHNAN, Divya ; KHAN, Amir ; MUNIRAJU, Yogendra Manjunath Bangalore ; M, Nikitha ; NAIR, Karthika ; RODRIGUES, Kavitha Iyer ; TIWARI, Anurag ; CHATTERJEE, Sohang ; PRASAD, Bhargav ; CHAKRABARTY, Subhra Prakash ; SRINIVASAN, Sankaranarayanan ; PATEL, Shivani ; RAO, Sahana Bhima ; DUBEY, Ashvini Kumar ; BHATTACHARJEE, Sanghamitra ; KAMANAGOWDA, Veeresha ; KUMAR, Santosh ; NATARAJAN, Bairavabalakumar ; SHARMA, Ankurina ; THANIGAIVEL, Aswini ; SHARMA, Rashmi ; SHENOY, Bharath Ravindra ; HORA, Anuradha ; MUKUNDA, Pavithra ; MURUGESAN, Sathyabalan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ES2837482TT33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>spa</language><creationdate>2021</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>MAITY, Sunit</creatorcontrib><creatorcontrib>DAKSHINAMURTHY, Pravin Kumar</creatorcontrib><creatorcontrib>MALIWALAVE, Amol</creatorcontrib><creatorcontrib>GHOSH, Maloy</creatorcontrib><creatorcontrib>HALAN, Vivek</creatorcontrib><creatorcontrib>UNNIKRISHNAN, Divya</creatorcontrib><creatorcontrib>KHAN, Amir</creatorcontrib><creatorcontrib>MUNIRAJU, Yogendra Manjunath Bangalore</creatorcontrib><creatorcontrib>M, Nikitha</creatorcontrib><creatorcontrib>NAIR, Karthika</creatorcontrib><creatorcontrib>RODRIGUES, Kavitha Iyer</creatorcontrib><creatorcontrib>TIWARI, Anurag</creatorcontrib><creatorcontrib>CHATTERJEE, Sohang</creatorcontrib><creatorcontrib>PRASAD, Bhargav</creatorcontrib><creatorcontrib>CHAKRABARTY, Subhra Prakash</creatorcontrib><creatorcontrib>SRINIVASAN, Sankaranarayanan</creatorcontrib><creatorcontrib>PATEL, Shivani</creatorcontrib><creatorcontrib>RAO, Sahana Bhima</creatorcontrib><creatorcontrib>DUBEY, Ashvini Kumar</creatorcontrib><creatorcontrib>BHATTACHARJEE, Sanghamitra</creatorcontrib><creatorcontrib>KAMANAGOWDA, Veeresha</creatorcontrib><creatorcontrib>KUMAR, Santosh</creatorcontrib><creatorcontrib>NATARAJAN, Bairavabalakumar</creatorcontrib><creatorcontrib>SHARMA, Ankurina</creatorcontrib><creatorcontrib>THANIGAIVEL, Aswini</creatorcontrib><creatorcontrib>SHARMA, Rashmi</creatorcontrib><creatorcontrib>SHENOY, Bharath Ravindra</creatorcontrib><creatorcontrib>HORA, Anuradha</creatorcontrib><creatorcontrib>MUKUNDA, Pavithra</creatorcontrib><creatorcontrib>MURUGESAN, Sathyabalan</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MAITY, Sunit</au><au>DAKSHINAMURTHY, Pravin Kumar</au><au>MALIWALAVE, Amol</au><au>GHOSH, Maloy</au><au>HALAN, Vivek</au><au>UNNIKRISHNAN, Divya</au><au>KHAN, Amir</au><au>MUNIRAJU, Yogendra Manjunath Bangalore</au><au>M, Nikitha</au><au>NAIR, Karthika</au><au>RODRIGUES, Kavitha Iyer</au><au>TIWARI, Anurag</au><au>CHATTERJEE, Sohang</au><au>PRASAD, Bhargav</au><au>CHAKRABARTY, Subhra Prakash</au><au>SRINIVASAN, Sankaranarayanan</au><au>PATEL, Shivani</au><au>RAO, Sahana Bhima</au><au>DUBEY, Ashvini Kumar</au><au>BHATTACHARJEE, Sanghamitra</au><au>KAMANAGOWDA, Veeresha</au><au>KUMAR, Santosh</au><au>NATARAJAN, Bairavabalakumar</au><au>SHARMA, Ankurina</au><au>THANIGAIVEL, Aswini</au><au>SHARMA, Rashmi</au><au>SHENOY, Bharath Ravindra</au><au>HORA, Anuradha</au><au>MUKUNDA, Pavithra</au><au>MURUGESAN, Sathyabalan</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Vectores para la clonación y expresión de proteínas, métodos y aplicaciones de estos</title><date>2021-06-30</date><risdate>2021</risdate><abstract>Una constructo de vector disenado para recibir un anticuerpo o un fragmento de este a partir de un fagemido que comprende al menos una region de clonacion o a partir de un vector de levadura que comprende al menos una region de clonacion, o, para transferir un anticuerpo o un fragmento de este a un vector de levadura que comprende al menos una region de clonacion, donde dicho constructo de vector contiene un casete de expresion que comprende: al menos una secuencia lider; al menos una region de clonacion para recibir un gen que codifica un peptido o proteina que se une selectivamente a un ligando biologicamente activo; al menos una secuencia de nucleotidos que codifica la region constante de la cadena pesada de inmunoglobulina o la region constante de la cadena ligera de inmunoglobulina, o fragmentos de estas, o una combinacion de la region constante de la cadena pesada de inmunoglobulina o un fragmento de esta y la region constante de la cadena ligera de inmunoglobulina o fragmento de esta, en donde dicha region constante comprende al menos una mutacion con respecto a la region constante de una inmunoglobulina nativa o fragmentos de esta; y al menos una secuencia de etiqueta recombinante o secuencia de acido nucleico codificante de seleccion; en donde la al menos una region de clonacion del casete de expresion comprende un sitio de clonacion multiple 1 (MCS I) y un sitio de clonacion multiple 2 (MCS II), un sitio de clonacion multiple 1 (MCS I) solo o un sitio de clonacion multiple 2 (MCS II) solo, y en donde MCS I comprende una combinacion de los sitios de restriccion NdeI y BglII y HindIII y AscI, y el MCS II comprende una combinacion de los sitios de restriccion NcoI y XbaI y NheI y NotI. The present disclosure relates to vectors for cloning and expressing genetic material including but not limiting to antibody gene or parts thereof and methods of generating said vectors. Said vectors express the antibody genes in different formats such as Fab or scFv as a part of intertransfer system, intratransfer system or direct cloning and expression in individual display systems. In particular, phage display technology is used to clone and screen potential antibody genes in phagemid which is followed by the transfer of said genes to yeast vector for further screening and identification of lead molecules against antigens. The present vectors have numerous advantages including uniquely designed inserts/expression cassettes resulting in efficient and smooth transfer of clonal population from phage to yeast vectors resulting in efficient library preparation and identification of lead molecules.</abstract><oa>free_for_read</oa></addata></record>
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subjects BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS THEREOF
CULTURE MEDIA
ENZYMOLOGY
METALLURGY
MICROBIOLOGY
MICROORGANISMS OR ENZYMES
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
PEPTIDES
PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS
SPIRITS
VINEGAR
WINE
title Vectores para la clonación y expresión de proteínas, métodos y aplicaciones de estos
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