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AI 繪圖提示詞:科研插圖的 S.S.V.D. 框架與 10 個範本

科研插圖專用的 AI 繪圖提示詞框架 S.S.V.D.,附 10 個可直接使用的提示詞範本,協助你用 AI 準確生成訊息傳遞路徑圖、晶體結構等科學插圖。

SciFig Team
SciFig Team
SciFig 編輯團隊
用 SciFig 生成的科學插圖,品質取決於你的 AI 繪圖提示詞。多數研究人員坐下來,輸入類似「畫一張細胞訊息傳遞路徑圖」的指令,然後對結果感到有些失望:一半的蛋白質不見了,配色像兒童教科書。這張科學插圖不能說錯,只是不是他們腦中想的那張。

意圖與產出之間的落差,並不是 AI 的限制,而是提示詞的問題,而且完全可以解決。

每週產出數十張可供發表插圖的資深研究人員,並沒有使用什麼特殊技巧。他們遵循一套簡單的思考框架:告訴模型要畫什麼、如何排列、看起來應該如何,以及要包含多少細節。一旦內化這個四部分結構,你的產出就能從堪用提升到出色。

把這套框架用在最新模型上

比較 Nano Banana 2.1 與 GPT Image 2.5 在科研插圖上的表現,從標註、版面到局部修改。這篇比較指南提供精簡的提示詞結構與精選的科學影像範例;Flare/Sunburst 比較則協助你選擇版本。

完美科學提示詞的組成

每一條好的科學提示詞都會回答四個問題。我們稱之為 S.S.V.D. 框架:
S.S.V.D. 提示詞框架四象限資訊圖:Subject(顯微鏡)、Style(色板)、Visualization(圖表)、Details(參數)匯入中央的提示詞(使用 SciFig 生成)
S.S.V.D. 提示詞框架四象限資訊圖:Subject(顯微鏡)、Style(色板)、Visualization(圖表)、Details(參數)匯入中央的提示詞(使用 SciFig 生成)
  • S — Subject(主題):你要描繪哪一個生物、化學或物理系統?用標準命名(HGNC 基因符號、IUPAC 名稱、解剖學術語)寫出具體的分子、結構或實體。
  • S — Structure(結構):各元素在空間上應如何排列?哪些元件位於上游或下游?需要傳達哪些關係:階層、先後順序,還是分支?
  • V — Visual Style(視覺風格):要採用什麼配色、線條粗細、標籤樣式與美學慣例?應該像 Nature 的方法圖,還是教學用插圖?(避開這些常見的風格錯誤。)
  • D — Detail Level(細節程度):模型應該納入什麼、省略什麼?細節不是越多越好,過於繁雜的圖會模糊重點。
面向要回答的問題範例
S — Subject(主題)什麼系統或概念?NF-κB 訊息傳遞路徑
S — Structure(結構)元素如何排列?線性串聯,由左至右
V — Visual Style(視覺風格)什麼美學風格?簡潔向量、Nature 風格
D — Detail Level(細節程度)納入/排除什麼?只放關鍵蛋白質,不含輔因子

把 S.S.V.D. 當成送出任何提示詞前的檢查清單。涵蓋全部四個面向的提示詞,表現穩定優於只處理一兩個面向的提示詞。所需時間極少,補上這些細節很少超過三十秒,修改輪數卻能大幅減少。

以下提示詞範例示範同一個需求的兩種寫法:

薄弱的提示詞:"Draw an apoptosis pathway."
S.S.V.D. 提示詞:"Create a publication-ready scientific illustration of the intrinsic apoptosis pathway. Show cytochrome c release from the mitochondria, APAF-1 apoptosome formation, caspase-9 activation, and downstream cleavage of executioner caspases 3 and 7. Arrange components top-to-bottom from mitochondrial membrane to nuclear fragmentation. Use a monochromatic blue palette with black labels, clean sans-serif font, and inhibitory arrows (blunt ends) distinct from activating arrows (filled arrowheads). Omit the extrinsic pathway to keep the scientific figure focused."

第二條提示詞大約只多了四十個單字,卻能省下兩到三輪修改。

10 個可直接使用的 AI 繪圖提示詞範本

以下範本可以直接複製、修改後當作 AI 繪圖指令送出。請把方括號中的預留位置換成你的分子、生物體或實驗細節。

領域專用科學詞彙樹:五個主要分支(生物、化學、物理、醫學、生物資訊),每個分支列出 4–5 個具體術語(使用 SciFig 生成)
領域專用科學詞彙樹:五個主要分支(生物、化學、物理、醫學、生物資訊),每個分支列出 4–5 個具體術語(使用 SciFig 生成)
10 類提示詞範本的 2×5 網格展示,涵蓋分子結構、細胞生物學、解剖、訊息傳遞路徑、實驗、摘要圖與統計(使用 SciFig 生成)
10 類提示詞範本的 2×5 網格展示,涵蓋分子結構、細胞生物學、解剖、訊息傳遞路徑、實驗、摘要圖與統計(使用 SciFig 生成)

1. 細胞訊息傳遞路徑

"Create a publication-ready cell signaling pathway diagram illustrating [pathway name, e.g., PI3K/AKT/mTOR]. Begin at the receptor ([receptor name]) at the plasma membrane and trace signal propagation through [key intermediates] to downstream effectors [transcription factors or functional outputs]. Use distinct arrow styles for phosphorylation (circled P), ubiquitination (circled Ub), and translocation events. Apply a white background with a two-color scheme ([primary color] for active components, grey for inactive). Label all proteins with their standard HGNC symbols. Include subcellular compartment labels (plasma membrane, cytoplasm, nucleus)."

2. 蛋白質結構示意圖

"Generate a schematic diagram of [protein name] domain architecture. Show the following domains from N-terminus to C-terminus: [list domains with approximate residue ranges, e.g., PH domain (aa 1–100), kinase domain (aa 150–400), regulatory C-tail (aa 401–480)]. Indicate known post-translational modification sites: phosphorylation at [residue numbers], ubiquitination at [residue numbers]. Use color-coded blocks for each domain with a consistent legend. Include a linear scale bar. Style: clean academic illustration suitable for a review article figure panel."

3. 實驗流程/操作步驟

"Create a step-by-step experimental workflow diagram for [protocol name, e.g., chromatin immunoprecipitation followed by sequencing (ChIP-seq)]. Depict the following sequential steps: [list steps in order]. Use rectangular boxes connected by downward arrows for each step. Inside each box, include the step name in bold and a one-line procedural note. Use [color] to highlight critical quality-control checkpoints at steps [numbers]. Apply a clean white background with light grey box fills and black text. Add estimated time annotations on the right margin."

4. 器官/組織剖面

"Illustrate a labeled cross-sectional diagram of [organ or tissue, e.g., human kidney cortex at the cellular level]. Show the following cellular layers and structures: [list layers/structures]. Use a naturalistic color palette ([skin/tissue tones]). Include leader lines with anatomical labels in a clean sans-serif font positioned outside the illustration boundary. Add a scale bar indicating [dimension]. Style should be suitable for a medical journal or textbook — scientifically accurate, not stylized."

5. 化學反應機構

"Draw a step-by-step organic reaction mechanism for [reaction name, e.g., serine protease-catalyzed peptide bond hydrolysis]. Show all intermediates: [list intermediates]. Use standard curved-arrow notation for electron movement. Label nucleophilic, electrophilic, and leaving-group species. Display partial charges (δ+ and δ−) at transition states. Arrange steps left-to-right in a single horizontal sequence. Use black structures on a white background. Include compound labels below each structure and reaction condition labels (pH, temperature) above each arrow."

6. 奈米粒子藥物遞送系統

"Create a scientific illustration of a [type of nanoparticle, e.g., lipid nanoparticle] drug delivery system for [therapeutic application, e.g., siRNA delivery to hepatocytes]. Depict the nanoparticle cross-section showing: outer PEG corona, lipid bilayer shell, aqueous core containing [cargo]. Show the delivery sequence in four panels: (1) systemic circulation, (2) receptor-mediated endocytosis at the target cell, (3) endosomal escape, (4) intracellular cargo release. Use a consistent color scheme: [color] for the particle, [color] for the biological membranes. Label all components. Include a particle size scale (~[diameter] nm) in the first panel."

7. 基因表現串聯反應

"Illustrate the gene expression cascade from extracellular signal to protein output for [signaling context, e.g., interferon-γ stimulation of macrophages]. Show the sequential steps: ligand binding → receptor activation → JAK kinase phosphorylation → STAT transcription factor dimerization → nuclear import → promoter binding at [target gene loci] → mRNA transcription → cytoplasmic translation → functional protein. Arrange vertically from extracellular space (top) to cytoplasm (bottom). Use dashed boxes to delineate nuclear events. Apply a blue-to-orange gradient to indicate signal progression. Label all molecular players."

8. 搭配原始影像的顯微圖版面

"Create a schematic layout with [N] empty placeholders for original microscopy images from [experimental conditions]. Label the placeholders A, B, C, and D, and provide space for the channel labels and factual captions. Do not generate or simulate microscopy observations, phenotypes, or measured results. Add scale-bar placeholders only; the author will supply the original images and bars based on actual acquisition calibration in a layout editor."

9. 臨床試驗設計流程圖

"Design a CONSORT-style clinical trial flowchart for a [trial type, e.g., phase III randomized controlled trial] studying [intervention] in [patient population]. Show: enrollment and eligibility screening (n = [number]); randomization with allocation ratios; [number] intervention arms with arm labels and dosing; follow-up time points at [weeks/months]; primary and secondary endpoint assessment; dropout/loss-to-follow-up at each stage. Use standard flowchart boxes (rectangles for processes, diamonds for decisions). Apply a clean white background with [color] shading for the intervention arms. Include placeholder n-values at each node."

10. 生態系交互作用圖

"Create a scientific ecosystem interaction diagram for [ecosystem or community, e.g., coral reef trophic network]. Show [N] key species or functional groups: [list species]. Represent trophic interactions with directed arrows (arrow points to consumer). Distinguish interaction types: predation (solid lines), mutualism (dashed lines), competition (double-headed lines). Size nodes proportional to biomass [or trophic level]. Use a consistent species color scheme from primary producers (green) to apex predators (red). Position nodes to reflect trophic levels vertically. Include a legend. Style: clean academic illustration with white background."

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探索該工具

常見的提示詞錯誤(與修正方式)

即使是熟悉 SciFig 等 AI 工具的研究人員,也常落入幾個可預期的陷阱。認得這些模式,就能在送出前自行修正。

雙欄指南:應納入(主題、風格、視角、標籤、色板)與應避免(模糊、互相矛盾、缺少比例)(使用 SciFig 生成)
雙欄指南:應納入(主題、風格、視角、標籤、色板)與應避免(模糊、互相矛盾、缺少比例)(使用 SciFig 生成)
提示詞修改前後比較:四列範例,左側為模糊提示詞與品質不佳的產出,右側為具體提示詞與高品質產出(使用 SciFig 生成)
提示詞修改前後比較:四列範例,左側為模糊提示詞與品質不佳的產出,右側為具體提示詞與高品質產出(使用 SciFig 生成)

錯誤 1:用籠統的類別名稱,而不是具體的識別名稱

修改前:"Show a receptor activating a kinase cascade."
修改後:"Show EGFR dimerization activating the RAS/RAF/MEK/ERK cascade, with specific phosphorylation events at EGFR Tyr1068, RAS GTP loading, and ERK1/2 dual phosphorylation at Thr202/Tyr204."
為什麼重要:籠統的詞彙只會換來籠統的產出。模型對經典分子及其結構特徵有豐富的知識,但前提是你要叫出它們的名字。使用具體命名,是最快見效的一項改進。

錯誤 2:忽略空間與關係脈絡

修改前:"Draw the complement system activation pathway."
修改後:"Draw the classical complement activation pathway arranged left-to-right. Begin with antibody-antigen complex and C1q binding on the left, progress through C4b2a C3 convertase formation in the center, and end with membrane attack complex (MAC) pore formation on the right. Use vertical lanes to separate the recognition, amplification, and effector phases."
為什麼重要:沒有空間指示,模型只能猜測版面。在訊息傳遞路徑與流程圖中,空間配置傳達的是邏輯:從上游到下游、由外到內、先後或平行。描述排列方式只需要約十個單字,卻能消除大多數版面失誤。

錯誤 3:沒有定義視覺風格

修改前:"Make a pathway diagram with a nice color scheme."
修改後:"Use a two-color palette: blue (#2C5F8A) for active/phosphorylated states, grey (#BDBDBD) for inactive states. White background. Label all proteins in 8pt Arial bold. Use 1.5pt line weight for arrows and 0.75pt for structural outlines."
為什麼重要:「好看」對模型來說毫無意義。模型會套用一種看似合理但隨意的預設美學,未必符合你投稿期刊的風格規範。定義顏色、字型與線條粗細只需三十秒,通常可省下一整輪修改。

錯誤 4:在一條提示詞中要求太多

修改前:"Show the entire MAPK pathway including all isoforms, all cross-talk with PI3K, the role of scaffold proteins, subcellular localizations at the plasma membrane and nucleus, phosphorylation and ubiquitination states, and inhibitor binding sites."
修改後(第一條提示詞):"Show the core RAS/RAF/MEK/ERK cascade from plasma membrane to nucleus. Include only the canonical components: RAS, BRAF, MEK1/2, ERK1/2. Show activation-state arrows and nuclear translocation."

接著再迭代:"Add the ERK-mediated negative feedback phosphorylation of SOS at Ser1132."

為什麼重要:塞得太滿的提示詞會產出雜亂、不連貫的圖。迭代式提示:先建立核心結構,再在後續輪次補充細節,效果穩定優於一開始就想把所有內容寫完。

錯誤 5:省略輸出限制

修改前:"Create a scientific figure of the cell cycle."
修改後:"Create a circular cell cycle diagram suitable for a two-column journal layout (max 84 mm width). Use a minimal style: white background, no decorative gradients. Ensure all text is legible at 300 DPI after scaling to final print size."
為什麼重要:在螢幕解析度下看起來很好的科學插圖,到了印刷尺寸,標籤可能無法辨識。請在提示詞中寫明最終輸出尺寸與解析度要求,讓模型一開始就以合適的大小配置元素。

進階技巧:反覆修正

單一提示詞很少能直接產出定稿。效率最高的研究人員,會把 SciFig 的 AI 生成插圖 當成多輪對話,而不是一次性的交易。
循環式提示詞迭代流程:初始提示詞 → 評估缺口 → 修正提示詞 → 改善產出,每一輪累積品質星等(使用 SciFig 生成)
循環式提示詞迭代流程:初始提示詞 → 評估缺口 → 修正提示詞 → 改善產出,每一輪累積品質星等(使用 SciFig 生成)

這個流程分為四個階段:

階段 1:核心結構提示詞。建立主要元件及其空間關係,接受一份不完美的初稿。目標是確認基本架構正確:分子對、階層對、流向對。
階段 2:風格修正。結構確認後,再加入視覺規格。"Keep the current layout. Switch to a monochromatic blue palette. Increase label font size by 20%. Change inhibitory arrows to blunt-ended T-bars."
階段 3:補充細節。加入階段 1 刻意省略的元素。"Add the IκBα resynthesis feedback loop from the nucleus back to the cytoplasm. Add a phosphorylation event marker at IKKβ Ser177."
階段 4:準備輸出。對照資料來源檢查蛋白質標籤與細胞區室邊界。選擇支援的輸出解析度,需要向量細修時使用 SVG 轉換,並以預定的投稿尺寸檢查最終檔案。

分階段進行,可以把核心結構的檢查與視覺修飾分開。先確認元件與關係,再處理外觀。每次修訂仍需對照來源核實,所需的迭代次數取決於圖本身與實際產出。

定點修正讓修改要求保持具體:"Add a boundary between the cytoplasm and nucleus." 重新生成後,也要再檢查圖的其他部分,因為局部指令也可能影響其他內容。

由表格計算而來的圖,例如散布圖、盒鬚圖與熱圖,請使用 DataChart,並可下載繪圖用的 Python 程式碼檢查流程。概念圖請使用 Illustration,可編輯的 SVG 流程圖則使用 FlowChart。

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提示

影響最大的單一提示詞改進,是把籠統的類別詞換成具體的分子識別名稱。從 "a receptor tyrosine kinase" 改成 "EGFR (HER1)"(四個單字),對產出準確度的提升通常比把提示詞總長度加倍還多。拿不準時,先把分子寫具體,再考慮風格。

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