Team:SJTU-BioX-Shanghai/Project/Subproject1/Modeling 2

Modeling-2: Expand aaRS Modulator

In aaRS Modulator, we have modified tRNA^Asp and aspartyl aminoacyl tRNA synthetase (AspRS). tRNA^Asp is modified so that it can recognize rare codon AGG. Aspartyl aminoacyl tRNA synthetase (AspRS) is modified so that it loses the specificity for original tRNA^Asp.

To expand our aaRS Modulator, we intend to modify the tRNA and aaRS of amino acids other than Asp. For tRNA, the anticodon can be mutated to base-pair rare codons other than AGG. For aminoacyl tRNA synthetase (aaRS), the function of the anticodon recognition should be lowered or eliminated.

The 20 aaRS can be classified into two types, one with their anticodon recognition domains at the protein’s terminus, the other with their anticodon recognition domains inside the protein. For the first type, removing the anticodon recognition domains may not influence the overall structure and the aminoacylation function of the enzyme. For the second type, removing the domain may lead to incorrect folding of the protein.

Type One

We have designed the truncated version of the 14 Type One proteins based on their structures. See the designs below.

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AspRS (PDB:1C0A)	MetRS (PDB:1PG2)	ValRS (PDB:1GAX)	IleRS (PDB:1FFY)
ThrRS (PDB:1QF6)	GluRS (PDB:2CV0)	PheRS (PDB:1EIY)	ArgRS (PDB:2ZUE)
TyrRS (PDB:1H3E)	CysRS (PDB:1U0B)	LysRS (PDB:1BBU)	HisRS (PDB:1KMM)
GlyRS (PDB:1GGM)	LeuRS (PDB:2BTE)

Type Two

After we have analyzed the structure of the proteins below, we believe directed evolution is needed to obtain the modified enzyme.

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TrpRS (PDB:2AKE)

ProRS (PDB:1H4Q)

SerRS (PDB:1SER)

AlaRS (PDB:3HXW)