Q.1.
Only one cycle of directed evolution cycle is sufficient to obtain the desired protein molecule.
Q.2.
The starting point of both rational and irrational protein design is a wild-type protein.
Q.3.
Which step is performed after the mutation of genes in directed evolution?
Q.4.
Which of the following is not a method of directed evolution?
Q.5.
Who pioneered phage-display technology?
Q.6.
In the case of monovalent display, the valency of display depends on the ratio of phage containing phagemid vector and helper phage at the time of infection.
Q.7.
Which of the following bacteriophage is used in phage-display technology?
Q.8.
Mis a filamentous phage and it contains a circular single-stranded DNA genome.
Q.9.
Which of the following is the major coat protein of M13?
Q.10.
Which of the following is not true for error-prone PCR?
Q.11.
Which of the following proteins are involved in initiating phage assembly and maintaining the stability of the viral particle?
Q.12.
In the case of a monovalent display, the protein fusion can be constructed in a phagemid vector that carries a copy of the viral capsid gene.
Q.13.
Which of the following is used to create a large library of mutants for a given protein gene?
Q.14.
In the case of polyvalent-display, all gp III are conjugated with peptide and this results in occasional loss of infectivity.
Q.15.
In the case of a polyvalent display, the proteins can be cloned directly into a viral vector as a fusion to a capsid protein.