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. Author manuscript; available in PMC: 2019 Sep 28.
Published in final edited form as: J Control Release. 2018 Aug 11;286:415–424. doi: 10.1016/j.jconrel.2018.08.018

Table 1.

Serum proteins bind to AAV9

Accession Description Fold increase
P02671 Fibrinogen alpha chain OS=Homo sapiens GN=FGA PE=1 SV=2 4.945652
P02675 Fibrinogen beta chain OS=Homo sapiens GN=FGB PE=1 SV=2
Fibrinogen gamma chain OS=Homo sapiens GN=FGG PE=1
4.974026
P02679 SV=3
Fibrinogen gamma chain (Fragment) OS=Homo sapiens
4.853614
C9JU00 GN=FGG PE=2 SV=1 8.362319
P02751 Fibronectin OS=Homo sapiens GN=FN1 PE=1 SV=4 5.405263
P00747 Plasminogen OS=Homo sapiens GN=PLG PE=1 SV=2
Platelet factor 4 variant OS=Homo sapiens GN=PF4V1 PE=1
3.232278
P10720 SV=1 1.466667
P04275 von Willebrand factor OS=Homo sapiens GN=VWF PE=1 SV=4
Alpha-1-acid glycoprotein 2 OS=Homo sapiens GN=ORM2
ND
P19652 PE=1 SV=2 ND

ND: indicates no detection of protein in control group

➢ Several serum proteins have a potential effect on AAV vascular permeability.

➢ Serum proteins enhance AAV9 global transduction in mice after systemic administration.

➢ Cryoprecipitate augment AAV9 global transduction in mice.

➢ Fibrinogen and cryoprecipitate slow down the clearance of AAV9 vector in the blood.