<b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>

<p dir="ltr">AsPC-1 pancreatic cancer cells were transfected with the VPg-GSDMDeng saRNA vaccine and subsequently cultured for 15 consecutive passages to evaluate sequence stability during prolonged intracellular replication. Total RNA was isolated from both the first-generation (P1)...

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Автор: Zunyong feng (22673801) (author)
Опубліковано: 2025
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author Zunyong feng (22673801)
author_facet Zunyong feng (22673801)
author_role author
dc.creator.none.fl_str_mv Zunyong feng (22673801)
dc.date.none.fl_str_mv 2025-11-24T12:08:14Z
dc.identifier.none.fl_str_mv 10.6084/m9.figshare.30694151.v1
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/_b_Engineered_b_b_VPg_b_b_b_b_saRNA_achieves_cap-independent_b_b_b_b_low-immunogenic_and_precise_b_b_b_b_encoding_of_therapeutic_proteins_b_b_in_vivo_b_b_b_/30694151
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Synthetic biology
AsPC-1 cells
saRNA vaccine
dc.title.none.fl_str_mv <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <p dir="ltr">AsPC-1 pancreatic cancer cells were transfected with the VPg-GSDMDeng saRNA vaccine and subsequently cultured for 15 consecutive passages to evaluate sequence stability during prolonged intracellular replication. Total RNA was isolated from both the first-generation (P1) transfected cells—used as the non-mutated reference control—and the 15th-generation (P15) cells. High-fidelity reverse transcription PCR (RT-PCR) was performed using a proofreading DNA polymerase to minimize polymerase-induced errors. The resulting amplicons were subjected to bidirectional Sanger sequencing using multiple forward primers (M13F, seq1F, seq2F, seq3F) to ensure complete coverage of the coding region and to detect low-frequency variants.</p><p dir="ltr">All raw chromatogram files (.ab1) and derivative sequence files (.seq) have been deposited in the public repository. Each .ab1 file corresponds to an individual sequencing reaction and retains unprocessed fluorescence trace data, peak calls, and Phred quality values.</p>
eu_rights_str_mv openAccess
id Manara_f2cd20c4e2f9466769c99b206fbb134b
identifier_str_mv 10.6084/m9.figshare.30694151.v1
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30694151
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>Zunyong feng (22673801)Synthetic biologyAsPC-1 cellssaRNA vaccine<p dir="ltr">AsPC-1 pancreatic cancer cells were transfected with the VPg-GSDMDeng saRNA vaccine and subsequently cultured for 15 consecutive passages to evaluate sequence stability during prolonged intracellular replication. Total RNA was isolated from both the first-generation (P1) transfected cells—used as the non-mutated reference control—and the 15th-generation (P15) cells. High-fidelity reverse transcription PCR (RT-PCR) was performed using a proofreading DNA polymerase to minimize polymerase-induced errors. The resulting amplicons were subjected to bidirectional Sanger sequencing using multiple forward primers (M13F, seq1F, seq2F, seq3F) to ensure complete coverage of the coding region and to detect low-frequency variants.</p><p dir="ltr">All raw chromatogram files (.ab1) and derivative sequence files (.seq) have been deposited in the public repository. Each .ab1 file corresponds to an individual sequencing reaction and retains unprocessed fluorescence trace data, peak calls, and Phred quality values.</p>2025-11-24T12:08:14ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.6084/m9.figshare.30694151.v1https://figshare.com/articles/dataset/_b_Engineered_b_b_VPg_b_b_b_b_saRNA_achieves_cap-independent_b_b_b_b_low-immunogenic_and_precise_b_b_b_b_encoding_of_therapeutic_proteins_b_b_in_vivo_b_b_b_/30694151CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/306941512025-11-24T12:08:14Z
spellingShingle <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
Zunyong feng (22673801)
Synthetic biology
AsPC-1 cells
saRNA vaccine
status_str publishedVersion
title <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
title_full <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
title_fullStr <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
title_full_unstemmed <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
title_short <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
title_sort <b>Engineered </b><b>VPg</b><b> </b><b>saRNA achieves cap-independent,</b><b> </b><b>low-immunogenic and precise</b><b> </b><b>encoding of therapeutic proteins </b><b>in vivo</b><b>.</b>
topic Synthetic biology
AsPC-1 cells
saRNA vaccine