Evidence map›Paper›PMID 40291415›Full record

ArticleBio-protocol2025

A Robust and Easy Protein Purification Method Using SpyDock-Modified Resin.

Xiaofeng Yang, Zhanglin Lin, Ya Xiang, Binrui Chen, Zisha Lao

Abstract read
In one paragraph

Article in Bio-protocol, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xiaofeng YangSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.
Zhanglin LinSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.
Ya XiangSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.
Binrui ChenSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.
Zisha LaoSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein purification is a critical step in both life sciences and biomanufacturing. Traditional affinity chromatography (AC) methods, including His-tag-based purification, provide high-purity proteins but are limited by the high cost of resins and the need for additional tag-removal steps. In this protocol, we present a reusable SpyDock-modified epoxy resin coupled with a pH-inducible self-cleaving intein for direct purification of proteins with authentic N-termini. This method enables efficient protein purification from cell lysates, achieving high purity (>90%) and yields comparable to the His-tag approach, without requiring tag removal. The SpyDock-modified resin protocol is robust, easy to implement, and cost-effective, making it suitable for both research and large-scale industrial applications. Key features • This protocol offers a robust and straightforward method for purifying proteins with authentic N-termini, eliminating the need for additional tag removal steps. • The approach achieves higher purity and comparable yields to the commercial His-tag method. • The SpyDock-modified epoxy resin is easy to prepare, cost-effective, and reusable.

Indexed as

Authentic N-terminiInteinProtein immobilizationProtein purificationSpy chemistrySpyDock-modified epoxy resin

Identifiers

PMID40291415
PMCPMC12021586

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.