RASP: rapid antibody functional screening by pentavalent phage display

The heavy-chain antibody variable domain (VHH) is the smallest antigen-binding domain of such antibodies, which are derived from camelids. In the past three decades, VHHs, which are also called single-domain antibodies, have been extensively used to target pathogens and/or toxins. Conventional screening methods, such as phage display, rely only on antibody-antigen binding as the sole criterion for selection. Despite being robust and high-throughput, such methods often require additional downstream experiments to identify VHH that neutralize their target. Here, we describe an innovative, high-throughput functional screening method, Rapid Antibody functional Screening by Pentavalent phage display (RASP), that incorporates purified antibody-displaying phages for virus neutralization assays, and thus can be used to directly identify neutralizing VHHs. As a proof-of-concept, we first displayed previously identified neutralizing VHHs specific for the spike proteins of SARS-CoV-2 and respiratory syncytial virus on phages and demonstrated a dose-dependent blockade of viral infection. We further improved our method by utilizing the pentavalent display feature of hyperphages. We showed that hyperphage-derived VHH phages were superior to helper phage-derived VHH phages in assaying viral neutralization potential. Thereafter, we applied RASP to identify multiple candidates by screening a semi-synthetic VHH library against recombinant vesicular stomatitis viruses pseudotyped with spike glycoproteins from SARS-CoV-2, Junin virus, and Ebola virus, featuring as case studies in antiviral antibody discovery. Further, we benchmarked RASP against established phage ELISA and next-generation sequencing methods. Overall, we successfully used RASP in the context of the discovery of antiviral VHHs, highlighting its broader applicability as a platform that can be used either in isolation or in conjunction with other functional screening methods to accelerate the discovery of antiviral VHHs.

Authors

Institutions

Publication Details

Journal
mAbs
Published
2026-02-09
DOI
https://doi.org/10.1080/19420862.2026.2627708
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

RASP: rapid antibody functional screening by pentavalent phage display

Kartik Chandran, Abhishek Dubey, Manpreet Kaur
mAbs
Monoclonal and Polyclonal Antibodies Research
article

RASP: rapid antibody functional screening by pentavalent phage display

Kartik Chandran, Abhishek Dubey, Manpreet Kaur
article en

Abstract

The heavy-chain antibody variable domain (VHH) is the smallest antigen-binding domain of such antibodies, which are derived from camelids. In the past three decades, VHHs, which are also called single-domain antibodies, have been extensively used to target pathogens and/or toxins. Conventional screening methods, such as phage display, rely only on antibody-antigen binding as the sole criterion for selection. Despite being robust and high-throughput, such methods often require additional downstream experiments to identify VHH that neutralize their target. Here, we describe an innovative, high-throughput functional screening method, Rapid Antibody functional Screening by Pentavalent phage display (RASP), that incorporates purified antibody-displaying phages for virus neutralization assays, and thus can be used to directly identify neutralizing VHHs. As a proof-of-concept, we first displayed previously identified neutralizing VHHs specific for the spike proteins of SARS-CoV-2 and respiratory syncytial virus on phages and demonstrated a dose-dependent blockade of viral infection. We further improved our method by utilizing the pentavalent display feature of hyperphages. We showed that hyperphage-derived VHH phages were superior to helper phage-derived VHH phages in assaying viral neutralization potential. Thereafter, we applied RASP to identify multiple candidates by screening a semi-synthetic VHH library against recombinant vesicular stomatitis viruses pseudotyped with spike glycoproteins from SARS-CoV-2, Junin virus, and Ebola virus, featuring as case studies in antiviral antibody discovery. Further, we benchmarked RASP against established phage ELISA and next-generation sequencing methods. Overall, we successfully used RASP in the context of the discovery of antiviral VHHs, highlighting its broader applicability as a platform that can be used either in isolation or in conjunction with other functional screening methods to accelerate the discovery of antiviral VHHs.

mAbsVol. 18(1)
Albert Einstein College of Medicine (US)
Openalex Percentile: Top 64%
Monoclonal and Polyclonal Antibodies Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.