tetano
Editor, Senior Moderator
Sci Adv
. 2022 Dec 9;8(49):eabo3977.
doi: 10.1126/sciadv.abo3977. Epub 2022 Dec 9.
Single-virus tracking reveals variant SARS-CoV-2 spike proteins induce ACE2-independent membrane interactions
Shaun M Christie[SUP] 1 [/SUP], Takuya Tada[SUP] 2 [/SUP], Yandong Yin[SUP] 1 [/SUP], Amit Bhardwaj[SUP] 1 [/SUP], Nathaniel R Landau[SUP] 2 [/SUP], Eli Rothenberg[SUP] 1 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became a global health crisis after its emergence in 2019. Replication of the virus is initiated by binding of the viral spike (S) protein to human angiotensin-converting enzyme 2 (ACE2) on the target cell surface. Mutations acquired by SARS-CoV-2 S variants likely influence virus-target cell interaction. Here, using single-virus tracking to capture these initial steps, we observe how viruses carrying variant S interact with target cells. Specificity for ACE2 occurs for viruses with the reference sequence or D614G mutation. Analysis of the Alpha, Beta, and Delta SARS-CoV-2 variant S proteins revealed a progressive altered cell interaction with a reduced dependence on ACE2. Notably, the Delta variant S affinity was independent of ACE2. These enhanced interactions may account for the increased transmissibility of variants. Knowledge of how mutations influence cell interaction is essential for vaccine development against emerging variants of SARS-CoV-2.
. 2022 Dec 9;8(49):eabo3977.
doi: 10.1126/sciadv.abo3977. Epub 2022 Dec 9.
Single-virus tracking reveals variant SARS-CoV-2 spike proteins induce ACE2-independent membrane interactions
Shaun M Christie[SUP] 1 [/SUP], Takuya Tada[SUP] 2 [/SUP], Yandong Yin[SUP] 1 [/SUP], Amit Bhardwaj[SUP] 1 [/SUP], Nathaniel R Landau[SUP] 2 [/SUP], Eli Rothenberg[SUP] 1 [/SUP]
Affiliations
- PMID: 36490345
- DOI: 10.1126/sciadv.abo3977
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became a global health crisis after its emergence in 2019. Replication of the virus is initiated by binding of the viral spike (S) protein to human angiotensin-converting enzyme 2 (ACE2) on the target cell surface. Mutations acquired by SARS-CoV-2 S variants likely influence virus-target cell interaction. Here, using single-virus tracking to capture these initial steps, we observe how viruses carrying variant S interact with target cells. Specificity for ACE2 occurs for viruses with the reference sequence or D614G mutation. Analysis of the Alpha, Beta, and Delta SARS-CoV-2 variant S proteins revealed a progressive altered cell interaction with a reduced dependence on ACE2. Notably, the Delta variant S affinity was independent of ACE2. These enhanced interactions may account for the increased transmissibility of variants. Knowledge of how mutations influence cell interaction is essential for vaccine development against emerging variants of SARS-CoV-2.