Lab+Life Scientist Feb/Mar 2022

Page 6

Marwan Alsarraj*, Biopharma Segment Manager, Digital Biology Group

Using CRISPR and transposons for CAR T cell production CAR T cells are most often manufactured using viruses, but new research is exploring the benefits of using alternative gene editing systems for this purpose.

O

ver the last decade, the CRISPR/

Cas (CRISPR) system has emerged as a cutting-edge tool for gene editing; however, CRISPR’s molecular origins are anything but new. These constructs are evolutionarily related to a long line of small but mighty DNA constructs called transposons that have been practising the technique of jumping into a host cell’s genetic material and rewriting it for hundreds of millions of years. Transposons have been part of our ecosystem for so long that their genetic code is intermingled with that of all life on Earth. To date, scientists have uncovered a mind-boggling array of different types of transposons that follow diverse, but sometimes

that researchers carefully weigh options and choose

and its distant relatives to understand the options

overlapping, mechanisms of action. And in some

the system that best meets their needs. No matter

researchers must weigh.

cases, organisms from bacteria to humans have

what method is used for cell manufacturing, the

CRISPR

managed to usurp these genetic acrobats for their

product must be confirmed to be both safe and

CRISPR-Cas systems are reprogrammable DNA

own benefit.

effective before it is delivered to a patient.

segments that code for an endonuclease and

Even now, researchers are leveraging the

guide RNA. The construct originally served as a bacterial immune system to target viral

based constructs to develop faster, safer and cheaper

Comparing and contrasting gene editing options

ways to manufacture CAR T cells. Each system has

What are the major gene editing constructs

guide RNA to target CRISPR to specific sites in

its own benefits and drawbacks, so it is important

available? Let’s take a quick look at CRISPR/Cas9

the genome of any cell. When combined with

unique qualities of CRISPR and other transposon-

6 | LAB+LIFE SCIENTIST - Feb/Mar 2022

infections. Now, researchers can engineer the

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