Insertion of a foreign sequence on capsid surface loops of human papillomavirus type 16 virus-like particles reduces their capacity to induce neutralizing antibodies and delineates a conformational neutralizing epitope.
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Identification of human papillomavirus type 16 L1 surface loops required for neutralization by human seraCharacterization of HPV16 L1 loop domains in the formation of a type-specific, conformational epitopeLessons learned from successful human vaccines: Delineating key epitopes by dissecting the capsid proteinsCrystal structures of four types of human papillomavirus L1 capsid proteins: understanding the specificity of neutralizing monoclonal antibodiesThe C-Terminal Arm of the Human Papillomavirus Major Capsid Protein Is Immunogenic and Involved in Virus-Host InteractionIdentification of neutralizing conformational epitopes on the human papillomavirus type 31 major capsid protein and functional implicationsNewcastle disease virus-like particles: preparation, purification, quantification, and incorporation of foreign glycoproteinsEfficient production of chimeric human papillomavirus 16 L1 protein bearing the M2e influenza epitope in Nicotiana benthamiana plants.Combinatorial approach to hepadnavirus-like particle vaccine designIdentification of the neutralizing epitopes of Merkel cell polyomavirus major capsid protein within the BC and EF surface loopsBinding and neutralization efficiencies of monoclonal antibodies, Fab fragments, and scFv specific for L1 epitopes on the capsid of infectious HPV particles.Vaccination, immune and gene therapy based on virus-like particles against viral infections and cancer.The DE and FG loops of the HPV major capsid protein contribute to the epitopes of vaccine-induced cross-neutralising antibodies.Viral nanoparticles and virus-like particles: platforms for contemporary vaccine design.Virus-like particles in vaccine development.Developments in virus-like particle-based vaccines for infectious diseases and cancer.Different applications of virus-like particles in biology and medicine: Vaccination and delivery systems.Human papillomavirus type 16 pseudovirions with few point mutations in L1 major capsid protein FG loop could escape actual or future vaccination for potential use in gene therapy.Positively charged synthetic peptides from structural proteins of papillomaviruses abrogate human papillomavirus infectivity.Expression of human papillomavirus 6b L1 protein in silkworm larvae and enhanced green fluorescent protein displaying on its virus-like particlesNanoparticle Vaccines Against Infectious Diseases
P2860
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P2860
Insertion of a foreign sequence on capsid surface loops of human papillomavirus type 16 virus-like particles reduces their capacity to induce neutralizing antibodies and delineates a conformational neutralizing epitope.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@en
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@nl
type
label
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@en
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@nl
prefLabel
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@en
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@nl
P2093
P1433
P1476
Insertion of a foreign sequenc ...... mational neutralizing epitope.
@en
P2093
Jean-Rémy Sadeyen
Marina Shkreli
Pierre Coursaget
Pierre-Yves Sizaret
Sylvie Tourne
P356
10.1016/S0042-6822(02)00134-4
P407
P577
2003-04-01T00:00:00Z