The phrase "ability to interact with multiple" is correct and usable in written English.
It can be used when discussing someone's or something's capacity to engage or communicate with several entities or systems simultaneously.
Example: "The software's ability to interact with multiple databases enhances its functionality and user experience."
Alternatives: "capacity to engage with several" or "capability to communicate with multiple".
Over the past two decades, it has become apparent that PPP1 versatility is achieved by its ability to interact with multiple targeting/regulatory subunits known as PPP1 interacting proteins – PIPs (Cohen, 2002; Virshup and Shenolikar, 2009).
Notably, TIP60 was recently identified as one of the six 'hub' genes uncovered in a large-scale genetic interaction screen in C. elegans, so characterized by their ability to interact with multiple other genes and with all of the developmental signaling pathways screened in the study [24].
One of the major advantages of these naturalistic chemicals is their ability to interact with multiple targets in the body resulting in a combined beneficial effect.
The good news is that in today's multi-screen world, the ability to interact with multiple devices has the potential to increase the odds of forming lasting user habits.
The ability to interact with multiple import receptors provides alternate pathways for nuclear localization of LANA.
These findings indicate that disordered IRs can provide the ability to interact with multiple different proteins.
In contrast, super generalists are expected to evolve and coevolve within megadiversified webs of interactions among free-living species mainly by evolving abilities to interact with multiple, distinct groups of partners.
Both of the Sox17 truncations and the point mutant maintained the ability to interact with Smad3 across multiple binding stringencies (Fig. 7C).
CD44 mediates multiple effects on cell behavior in part through its ability to interact with HA [ 7] and due to the presence of multiple isoforms of CD44 that arise from N- and O-glycosylation, alternative splicing, and proteolytic cleavage.
A distinguishing feature of both proteins is their ability to interact with TGFβ family growth factors, Notch and Notch ligands, and multiple elastic fiber proteins.
Maturation of LRP to the trans-Golgi network is partially dependent upon the presence of LRP-receptor-associated protein (RAP), which binds to LRP at multiple sites to block the receptor's ability to interact with its ligands [11].
