Zumutor Biologics Inc.

Veeresha Kamanagowda

Bharath Ravindra Shenoy

Sunit Maity

Vivek Halan

Sanghamitra Bhattacharjee

Maloy Ghosh

Kavitha Iyer Rodrigues

Sahana Bhima Rao

Divya Unnikrishnan

Sohang Chatterjee

Bhargav Prasad

Anuradha Hora

Sankaranarayanan Srinivasan

Aswini Thanigaivel

Karthika Nair

Yogendra Manjunath Bangalore Muniraju

Bairavabalakumar Natarajan

Sathyabalan Murugesan

Subhra Prakash Chakrabarty

Ashvini Kumar Dubey

Amir Khan

Pravin Kumar Dakshinamurthy

Pavithra Mukunda

Amol Maliwalave

Anurag Tiwari

Santosh Kumar

Shivani Patel

Ankurina Sharma

Nikitha M

Rashmi Sharma

Nikitha Markanda

Jahnabi Hazarika

Maliwalave Amol

Yogendra Manjunath Muniraju

Sankarnarayanan Srinivasan

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.

Vectors for cloning and expression of proteins, methods and applications thereof

The present disclosure relates to a method of generating an antibody library, not limiting to a human na&#xef;ve antibody gene expression library encompassing a pool of nucleic acid sequences derived from a natural antibody repertoire comprising humoral immunity from healthy and genetically diverse human populations. More specifically, the method employs a combination of phage and/or yeast antibody surface display concept which allows to screen large antibody library size and facilitates better folding of antibody structure. The present disclosure also relates to a human na&#xef;ve antibody library generated by employing the process of the present disclosure, a set of primers employed in the method and application(s) of said antibody library.

Method of generating an antibody na&#xef;ve library, said library and application(s) thereof

The present disclosure relates to methods of obtaining cell with disrupted fucosylation and obtaining afucosylated protein. The present disclosure employs the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology in a protein producing cell line to produce afucosylated protein. The resulting protein, specifically the resulting monoclonal antibody is completely afucosylated and reveals higher degree of antibody dependent cellular cytotoxicity.

Afucosylated protein, cell expressing said protein and associated methods

The present disclosure relates to a method of generating an antibody library, not limiting to a synthetic antibody gene expression library built on pool of consensus nucleic acid sequences by using codon replacement technology. The present disclosure also relates to a synthetic antibody library generated by employing the method of the present disclosure and application(s) of said antibody library.

Method of generating a synthetic antibody library, said library and application(s) thereof

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Bengaluru, India

Veeresha Kamanagowda